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Volumn 23, Issue 3, 2011, Pages 190-214

Assignment of absolute configuration using chiral reagents and NMR spectroscopy

Author keywords

absolute configuration; absolute stereochemistry; chiral derivatizing agents; chiral solvating agents; NMR spectroscopy

Indexed keywords

ALCOHOL DERIVATIVE; ALDEHYDE DERIVATIVE; ALKENE DERIVATIVE; AMINE; AMINE OXIDE; AMINO ACID DERIVATIVE; BETA AMINO ACID; CARBOHYDRATE DERIVATIVE; CARBOXYLIC ACID DERIVATIVE; EPOXIDE; ESTER DERIVATIVE; HYDROCARBON; IMINE; ISOCYANIC ACID DERIVATIVE; KETONE DERIVATIVE; LACTONE DERIVATIVE; METAL COMPLEX; NITROGEN DERIVATIVE; OXAZIRIDINE DERIVATIVE; PHOSPHATE; PHOSPHINE DERIVATIVE; PHOSPHINE OXIDE DERIVATIVE; PHOSPHONIC ACID DERIVATIVE; PHOSPHORUS DERIVATIVE; PHTHALIDE DERIVATIVE; POLYOL; REAGENT; SULFOXIDE; THIOL DERIVATIVE;

EID: 79951503684     PISSN: 08990042     EISSN: 1520636X     Source Type: Journal    
DOI: 10.1002/chir.20889     Document Type: Review
Times cited : (141)

References (251)
  • 2
    • 33947085552 scopus 로고
    • Nuclear magnetic resonance enantiomer reagents. Configurational correlations via nuclear magnetic resonance chemical shifts of diastereomeric mandelate, O-methylmandelate, and α-methoxy-α- trifluoromethylphenylacetate (MTPA) esters
    • Dale JA, Mosher HS,. Nuclear magnetic resonance enantiomer reagents. Configurational correlations via nuclear magnetic resonance chemical shifts of diastereomeric mandelate, O-methylmandelate, and α-methoxy-α- trifluoromethylphenylacetate (MTPA) esters. J Am Chem Soc 1973; 95: 512-519.
    • (1973) J Am Chem Soc , vol.95 , pp. 512-519
    • Dale, J.A.1    Mosher, H.S.2
  • 3
    • 2142858450 scopus 로고
    • High-field FT NMR application of Mosher's method. The absolute configuration of marine terpenoids
    • Ohtani I, Kusumi T, Kashman Y, Kakisawa H,. High-field FT NMR application of Mosher's method. The absolute configuration of marine terpenoids. J Am Chem Soc 1991; 113: 4092-4096.
    • (1991) J Am Chem Soc , vol.113 , pp. 4092-4096
    • Ohtani, I.1    Kusumi, T.2    Kashman, Y.3    Kakisawa, H.4
  • 4
    • 38449102399 scopus 로고    scopus 로고
    • Mosher ester analysis for the determination of absolute configuration of stereogenic (chiral) carbinol carbons
    • Hoye TR, Jeffrey CS, Shao F,. Mosher ester analysis for the determination of absolute configuration of stereogenic (chiral) carbinol carbons. Nat Protoc 2007; 2: 2451-2458.
    • (2007) Nat Protoc , vol.2 , pp. 2451-2458
    • Hoye, T.R.1    Jeffrey, C.S.2    Shao, F.3
  • 5
    • 12744252858 scopus 로고    scopus 로고
    • Novel chiral molecular tools for preparation of enantiopure alcohols by resolution and simultaneous determination of their absolute configurations by the 1H NMR anisotropy method
    • Kasai Y, Naito J, Kuwahara S, Watanabe M, Ichikawa A, Harada N,. Novel chiral molecular tools for preparation of enantiopure alcohols by resolution and simultaneous determination of their absolute configurations by the 1H NMR anisotropy method. J Synth Org Chem Jpn 2004; 62: 48-61.
    • (2004) J Synth Org Chem Jpn , vol.62 , pp. 48-61
    • Kasai, Y.1    Naito, J.2    Kuwahara, S.3    Watanabe, M.4    Ichikawa, A.5    Harada, N.6
  • 6
    • 43249096726 scopus 로고    scopus 로고
    • 1H NMR anisotropy
    • DOI 10.1002/chir.20478
    • Harada N,. Determination of absolute configurations by X-r (Pubitemid 351656173)
    • (2008) Chirality , vol.20 , Issue.5 , pp. 691-723
    • Harada, N.1
  • 7
    • 0033534444 scopus 로고    scopus 로고
    • 9-anthrylmethoxyacetic acid esterification shifts-correlation with the absolute stereochemistry of secondary alcohols
    • PII S0040402098010552
    • Seco JM, Quiñoá E, Riguera R,. 9-Anthrylmethoxyacetic acid esterification shifts-correlation with the absolute stereochemistry of secondary alcohols. Tetrahedron 1999; 55: 569-584. (Pubitemid 29017860)
    • (1999) Tetrahedron , vol.55 , Issue.2 , pp. 569-584
    • Seco, J.M.1    Quinoa, E.2    Riguera, R.3
  • 8
    • 0001376826 scopus 로고
    • Conformational structure and dynamics of arylmethoxyacetates: DNMR spectroscopy and aromatic shielding effect
    • Latypov SK, Seco JM, Quiñoá E, Riguera R,. Conformational structure and dynamics of arylmethoxyacetates: DNMR spectroscopy and aromatic shielding effect. J Org Chem 1995; 60: 504-515.
    • (1995) J Org Chem , vol.60 , pp. 504-515
    • Latypov, S.K.1    Seco, J.M.2    Quiñoá, E.3    Riguera, R.4
  • 10
    • 0035835949 scopus 로고    scopus 로고
    • Determination of the absolute stereochemistry of alcohols and amines by NMR of the group directly linked to the chiral derivatizing reagent
    • DOI 10.1016/S0040-4020(01)00056-4, PII S0040402001000564
    • Latypov SK, Galiullina NF, Aganov AV, Kataev VE, Riguera R,. Determination of the absolute stereochemistry of alcohols and amines by NMR of the group directly linked to the chiral derivatizing reagent. Tetrahedron 2001; 57: 2231-2236. (Pubitemid 32200542)
    • (2001) Tetrahedron , vol.57 , Issue.11 , pp. 2231-2236
    • Latypov, S.K.1    Galiullina, N.F.2    Aganov, A.V.3    Kataev, V.E.4    Riguera, R.5
  • 11
    • 10044266568 scopus 로고    scopus 로고
    • 1H NMR spectroscopy
    • DOI 10.1021/ol0479489
    • Takeuchi Y, Fujisawa H, Noyori R,. A very reliable method for determination of absoute configuration of chiral secondary alcohols by 1H NMR spectroscopy. Org Lett 2004; 6: 4607-4610. (Pubitemid 39611822)
    • (2004) Organic Letters , vol.6 , Issue.24 , pp. 4607-4610
    • Takeuchi, Y.1    Fujisawa, H.2    Noyori, R.3
  • 12
    • 37049084316 scopus 로고
    • The remarkably high reactivity of α-cyano-α- fluorophenylacetyl chloride (CFPA-CI) towards hindered nucleophiles in enantiomeric excess determination
    • Takeuchi Y, Itoh N, Koizumi T,. The remarkably high reactivity of α-cyano-α-fluorophenylacetyl chloride (CFPA-CI) towards hindered nucleophiles in enantiomeric excess determination. Chem Commun 1992; 1514-1515.
    • (1992) Chem Commun , pp. 1514-1515
    • Takeuchi, Y.1    Itoh, N.2    Koizumi, T.3
  • 13
    • 0032568272 scopus 로고    scopus 로고
    • 1H NMR with O-substituted mandelate derivatives
    • DOI 10.1016/S0040-4039(98)00059-8, PII S0040403998000598
    • Chataigner I, Lebreton J, Durand D, Guingant A, Villiéras J,. A new approach for the determination of the absolute configuration of secondary alcohols by 1H NMR with O-substituted mandelate derivatives. Tetrahedron Lett 1998; 39: 1759-1762. (Pubitemid 28204375)
    • (1998) Tetrahedron Letters , vol.39 , Issue.13 , pp. 1759-1762
    • Chataigner, I.1    Lebreton, J.2    Durand, D.3    Guingant, A.4    Villieras, J.5
  • 14
    • 0942277395 scopus 로고    scopus 로고
    • The assignment of absolute configuration by NMR
    • Seco JM, Quinoa E, Riguera R,. The assignment of absolute configuration by NMR. Chem Rev 2004; 104: 17-117.
    • (2004) Chem Rev , vol.104 , pp. 17-117
    • Seco, J.M.1    Quinoa, E.2    Riguera, R.3
  • 15
    • 33947303494 scopus 로고
    • Nuclear magnetic resonance nonequivalence of diastereomeric esters of α-substituted phenylacetic acids for the determination of stereochemical purity
    • Dale JA, Mosher HS,. Nuclear magnetic resonance nonequivalence of diastereomeric esters of α-substituted phenylacetic acids for the determination of stereochemical purity. J Am Chem Soc 1968; 90: 3732-3738.
    • (1968) J Am Chem Soc , vol.90 , pp. 3732-3738
    • Dale, J.A.1    Mosher, H.S.2
  • 16
    • 33845376028 scopus 로고
    • On the use of the O-methylmandelate ester for establishment of absolute configuration of secondary alcohols
    • Trost BM, Belletire JL, Godleski S, McDougal PG, Balkovec JM,. On the use of the O-methylmandelate ester for establishment of absolute configuration of secondary alcohols. J Org Chem 1986; 51: 2370-2374.
    • (1986) J Org Chem , vol.51 , pp. 2370-2374
    • Trost, B.M.1    Belletire, J.L.2    Godleski, S.3    McDougal, P.G.4    Balkovec, J.M.5
  • 17
    • 48349138800 scopus 로고    scopus 로고
    • Resin-bound chiral derivatizing agents for assignment of configuration by NMR spectroscopy
    • Porto S, Seco JM, Espinosa JF, Quinoa E, Riguera R,. Resin-bound chiral derivatizing agents for assignment of configuration by NMR spectroscopy. J Org Chem 2008; 73: 5714-5722.
    • (2008) J Org Chem , vol.73 , pp. 5714-5722
    • Porto, S.1    Seco, J.M.2    Espinosa, J.F.3    Quinoa, E.4    Riguera, R.5
  • 18
    • 0028861537 scopus 로고
    • Determination of the absolute configuration of alcohols by low temperature 1H NMR of aryl(methoxy)acetates
    • Seco JM, Latypov S, Quiñoá E, Riguera R,. Determination of the absolute configuration of alcohols by low temperature 1H NMR of aryl(methoxy)acetates. Tetrahedron: Asymmetry 1995; 6: 107-110.
    • (1995) Tetrahedron: Asymmetry , vol.6 , pp. 107-110
    • Seco, J.M.1    Latypov, S.2    Quiñoá, E.3    Riguera, R.4
  • 19
    • 0037189213 scopus 로고    scopus 로고
    • 1H NMR: In situ complexation of α-methoxyphenylacetic acid esters with barium(II)
    • DOI 10.1021/jo0256989
    • García R, Seco JM, Vázquez SA, Quiñoá E, Riguera R,. Absolute configuration of secondary alcohols by 1H NMR: in situ complexation of α-methoxyphenylacetic acid esters with barium(II). J Org Chem 2002; 67: 4579-4589. (Pubitemid 34700821)
    • (2002) Journal of Organic Chemistry , vol.67 , Issue.13 , pp. 4579-4589
    • Garcia, R.1    Seco, J.M.2    Vazquez, S.A.3    Quinoa, E.4    Riguera, R.5
  • 20
    • 0001384141 scopus 로고
    • Use of shift reagent with diastereomeric MTPA esters for determination of configuration and enantiomeric purity of secondary carbinols in 1H NMR spectroscopy
    • Yamaguchi S, Yasuhara F, Kabuto K,. Use of shift reagent with diastereomeric MTPA esters for determination of configuration and enantiomeric purity of secondary carbinols in 1H NMR spectroscopy. Tetrahedron 1976; 32: 1363-1367.
    • (1976) Tetrahedron , vol.32 , pp. 1363-1367
    • Yamaguchi, S.1    Yasuhara, F.2    Kabuto, K.3
  • 21
    • 0343725486 scopus 로고
    • Use of shift reagent with MTPA derivatives in 1H NMR spectroscopy. II. Determination of absolute configuration and diastereomeric composition of secondary carbinols in epimeric mixture
    • Yamaguchi S, Yasuhara F,. Use of shift reagent with MTPA derivatives in 1H NMR spectroscopy. II. Determination of absolute configuration and diastereomeric composition of secondary carbinols in epimeric mixture. Tetrahedron Lett 1977; 18: 16 89-92.
    • (1977) Tetrahedron Lett , vol.18 , Issue.16 , pp. 89-92
    • Yamaguchi, S.1    Yasuhara, F.2
  • 22
    • 0037077802 scopus 로고    scopus 로고
    • Use of diamagnetic lanthanide complex for extending the scope of NMR determination of absolute configuration by the modified Mosher's method
    • Omata K, Fujiwara T, Kabuto K,. Use of diamagnetic lanthanide complex for extending the scope of NMR determination of absolute configuration by the modified Mosher's method. Tetrahedron: Asymmetry 2002; 13: 1655-1662.
    • (2002) Tetrahedron: Asymmetry , vol.13 , pp. 1655-1662
    • Omata, K.1    Fujiwara, T.2    Kabuto, K.3
  • 23
    • 21844475636 scopus 로고    scopus 로고
    • 1H-NMR and HPLC after labeling with a chiral derivatization reagent, 2-(2,3- anthracenedicarboximide)cyclohexane carboxylic acid
    • DOI 10.1002/chir.20141
    • Ohtaki T, Akasaka K, Kabuto C, Ohrui H,. Chiral discrimination of secondary alcohols by both 1H-NMR and HPLC after labeling with a chiral derivatization reagent, 2-(2,3-anthracenedicarboximide)cyclohexane carboxylic acid. Chirality 2005; 17: S171-S176. (Pubitemid 40962078)
    • (2005) Chirality , vol.17 , Issue.SUPPL.
    • Ohtaki, T.1    Akasaka, K.2    Kabuto, C.3    Ohrui, H.4
  • 24
    • 0037034361 scopus 로고    scopus 로고
    • Toward the creation of NMR databases in chiral solvents: Bidentate chiral NMR solvents for assignment of the absolute configuration of acyclic secondary alcohols
    • Kobayashi Y, Hayashi N, Kishi Y,. Toward the creation of NMR databases in chiral solvents: bidentate chiral NMR solvents for assignment of the absolute configuration of acyclic secondary alcohols. Org Lett 2002; 4: 411-414.
    • (2002) Org Lett , vol.4 , pp. 411-414
    • Kobayashi, Y.1    Hayashi, N.2    Kishi, Y.3
  • 25
    • 11444259272 scopus 로고    scopus 로고
    • Application of chiral lanthanide shift reagents for assignment of absolute configuration of alcohols
    • DOI 10.1021/ol048061f
    • Ghosh I, Zeng H, Kishi Y,. Application of chiral lanthanide shift reagents for assignment of absolute configuration of alcohols. Org Lett 2004; 6: 4715-4718. (Pubitemid 40081628)
    • (2004) Organic Letters , vol.6 , Issue.25 , pp. 4715-4718
    • Ghosh, I.1    Zeng, H.2    Kishi, Y.3
  • 27
    • 79951480698 scopus 로고
    • Application of 1H NMR-Eu(fod)3-shifted spectra for the determination of the enantiomeric composition and absolute configuration of secondary alcohols, using (-)-ω-camphanic esters
    • Jurczak J, Konowal A, Krawczyk Z, Ejchart A,. Application of 1H NMR-Eu(fod)3-shifted spectra for the determination of the enantiomeric composition and absolute configuration of secondary alcohols, using (-)-ω-camphanic esters. Org Magn Reson 1981; 17: 50-52.
    • (1981) Org Magn Reson , vol.17 , pp. 50-52
    • Jurczak, J.1    Konowal, A.2    Krawczyk, Z.3    Ejchart, A.4
  • 28
    • 0033522862 scopus 로고    scopus 로고
    • Conformational analysis of MNCB (MBNC) esters and amides: Promising chiral reagents for stereoselective applications
    • DOI 10.1016/S0040-4020(99)00356-7, PII S0040402099003567
    • Latypov SK, Aganov AV, Tahara S, Fukushi Y,. Conformational analysis of MNCB (MBNC) esters and amides: promising chiral reagents for stereoselective applications. Tetrahedron 1999; 55: 7305-7318. (Pubitemid 29256131)
    • (1999) Tetrahedron , vol.55 , Issue.23 , pp. 7305-7318
    • Latypov, S.K.1    Aganov, A.V.2    Tahara, S.3    Fukushi, Y.4
  • 29
    • 0028212262 scopus 로고
    • A new method for establishment of absolute configurations of secondary alcohols by NMR spectroscopy
    • DOI 10.1016/S0040-4039(00)75848-5
    • Fukushi Y, Yajima C, Mizutani J,. A new method for establishment of absolute configurations of secondary alcohols by NMR spectroscopy. Tetrahedron Lett 1994; 35: 599-602. (Pubitemid 24071923)
    • (1994) Tetrahedron Letters , vol.35 , Issue.4 , pp. 599-602
    • Fukushi, Y.1    Yajima, C.2    Mizutani, J.3
  • 30
    • 0012683326 scopus 로고    scopus 로고
    • 1H NMR determination of absolute configuration of 1- or 2-aryl-substituted alcohols and amines by means of their diastereomers: Novel separation technique of diastereomeric derivatives of pyridyl alcohols by extraction
    • Matsugi M, Itoh K, Nojima M, Hagimoto Y, Kita Y,. 1H NMR determination of absolute configuration of 1- or 2-aryl-substituted alcohols and amines by means of their diastereomers: novel separation technique of diastereomeric derivatives of pyridyl alcohols by extraction. Chem Eur J 2002; 8: 5551-5564.
    • (2002) Chem Eur J , vol.8 , pp. 5551-5564
    • Matsugi, M.1    Itoh, K.2    Nojima, M.3    Hagimoto, Y.4    Kita, Y.5
  • 31
    • 84985532520 scopus 로고
    • Stereoelectronic effects and chiral recognition: A natural system of relationships between chiral compounds based on selectivities in the formation of acetals
    • Noe CR, Knollmüller M, Göstl G, Oberhauser B, Völlenkle H,. Stereoelectronic effects and chiral recognition: a natural system of relationships between chiral compounds based on selectivities in the formation of acetals. Angew Chem Int Ed Engl 1987; 26: 442-444.
    • (1987) Angew Chem Int Ed Engl , vol.26 , pp. 442-444
    • Noe, C.R.1    Knollmüller, M.2    Göstl, G.3    Oberhauser, B.4    Völlenkle, H.5
  • 32
    • 84988121035 scopus 로고    scopus 로고
    • Chiral lactols. XIII. on the determination of the absolute configuration of aromatic cyanohydrins and structurally related compounds
    • Noe CR, Knollmüller M, Gärtner P, Katikarides E, Gaischin L, Völlenkle H,. Chiral lactols. XIII. On the determination of the absolute configuration of aromatic cyanohydrins and structurally related compounds. Liebigs Ann Chem 1995: 1353-1360.
    • Liebigs Ann Chem , vol.1995 , pp. 1353-1360
    • Noe, C.R.1    Knollmüller, M.2    Gärtner, P.3    Katikarides, E.4    Gaischin, L.5    Völlenkle, H.6
  • 33
    • 42049122153 scopus 로고    scopus 로고
    • Carbon-13 chemical shifts of isoprenoid-β-D-glucopyranosides and -β-D-mannopyranosides. Stereochemical influences of aglycone alcohols
    • Kasai R, Suzuo M, Asakawa J, Tanaka O,. Carbon-13 chemical shifts of isoprenoid-β-D-glucopyranosides and -β-D-mannopyranosides. Stereochemical influences of aglycone alcohols. Tetrahedron Lett 1977: 175-178.
    • Tetrahedron Lett , vol.1977 , pp. 175-178
    • Kasai, R.1    Suzuo, M.2    Asakawa, J.3    Tanaka, O.4
  • 34
    • 33947094112 scopus 로고
    • Determination of the absolute configuration of a secondary hydroxy group in a chiral secondary alcohol using glycosidation shifts in carbon-13 nuclear magnetic resonance spectroscopy
    • Seo S, Tomita Y, Tori K, Yoshimura Y,. Determination of the absolute configuration of a secondary hydroxy group in a chiral secondary alcohol using glycosidation shifts in carbon-13 nuclear magnetic resonance spectroscopy. J Am Chem Soc 1978; 100: 3331-3339.
    • (1978) J Am Chem Soc , vol.100 , pp. 3331-3339
    • Seo, S.1    Tomita, Y.2    Tori, K.3    Yoshimura, Y.4
  • 35
    • 31644436433 scopus 로고    scopus 로고
    • Monosaccharides as internal probes for the determination of the absolute configuration of 2-butanol
    • DOI 10.1002/mrc.1735
    • Seroka P, Plosinski M, Czub J, Sowinski P, Pawlak,. Monosaccharides as internal probes for the determination of the absolute configuration of 2-butanol. Magn Reson Chem 2006; 44: 132-138. (Pubitemid 43171602)
    • (2006) Magnetic Resonance in Chemistry , vol.44 , Issue.2 , pp. 132-138
    • Seroka, P.1    Plosinski, M.2    Czub, J.3    Sowinski, P.4    Pawlak, J.5
  • 36
    • 0344867952 scopus 로고
    • Determination of the absolute configuration of chiral secondary alcohols from tetra-O-acetylglucosidation-induced 1H nuclear magnetic resonance shifts
    • Faghih R, Fontaine C, Horibe I, Imamura PM, Lukacs G, Olesker A, Seo S,. Determination of the absolute configuration of chiral secondary alcohols from tetra-O-acetylglucosidation-induced 1H nuclear magnetic resonance shifts. J Org Chem 1985; 50: 4918-4920.
    • (1985) J Org Chem , vol.50 , pp. 4918-4920
    • Faghih, R.1    Fontaine, C.2    Horibe, I.3    Imamura, P.M.4    Lukacs, G.5    Olesker, A.6    Seo, S.7
  • 37
    • 0000679433 scopus 로고
    • Tetra-O-benzoylglucosylation: A new 1H nuclear magnetic resonance method for determination of the absolute configuration of secondary alcohols
    • Trujillo M, Morales EQ, Vázquez JT,. Tetra-O-benzoylglucosylation: a new 1H nuclear magnetic resonance method for determination of the absolute configuration of secondary alcohols. J Org Chem 1994; 59: 6637-6642.
    • (1994) J Org Chem , vol.59 , pp. 6637-6642
    • Trujillo, M.1    Morales, E.Q.2    Vázquez, J.T.3
  • 38
    • 0029038522 scopus 로고
    • CD and 1H NMR study of the rotational population dependence of the hydroxymethyl group in β glucopyranosides on the aglycon and its absolute configuration
    • Morales EQ, Padrõn JI, Trujillo M, Vázquez JT,. CD and 1H NMR study of the rotational population dependence of the hydroxymethyl group in β glucopyranosides on the aglycon and its absolute configuration. J Org Chem 1995; 60: 2537-2548.
    • (1995) J Org Chem , vol.60 , pp. 2537-2548
    • Morales, E.Q.1    Padrõn, J.I.2    Trujillo, M.3    Vázquez, J.T.4
  • 39
    • 0030941721 scopus 로고    scopus 로고
    • 13C nuclear magnetic resonance method to determine the absolute configuration of secondary alcohols
    • DOI 10.1016/S0040-4020(97)00291-3, PII S0040402097002913
    • Kobayashi M,. The fucofuranoside method, a new 1H and 13C nuclear magnetic resonance method to determine the absolute configuration of secondary alcohols. Tetrahedron 1997; 53: 5973-5994. (Pubitemid 27174351)
    • (1997) Tetrahedron , vol.53 , Issue.17 , pp. 5973-5994
    • Kobayashi, M.1
  • 40
    • 0001988773 scopus 로고
    • Dynamic NMR studies of diastereomeric carbamates: Implications toward the determination of relative configuration by NMR
    • Pirkle WH, Simmons KA, Boeder CW,. Dynamic NMR studies of diastereomeric carbamates: implications toward the determination of relative configuration by NMR. J Org Chem 1979; 44: 4891-4896.
    • (1979) J Org Chem , vol.44 , pp. 4891-4896
    • Pirkle, W.H.1    Simmons, K.A.2    Boeder, C.W.3
  • 42
    • 0242499866 scopus 로고    scopus 로고
    • (S)-2-chloro-2-fluoroethanoyl isocyanate, a chiral derivative of trichloroacetyl isocyanate
    • DOI 10.1002/chir.10231
    • Vodicka P, Streinz L, Koutek B, Budešínský M, Ondrácek J, Císarova I,. (S)-2-Chloro-2-fluoroethanoyl isocyanate, a chiral derivative of trichloroacetyl isocyanate. Chirality 2003; 15: 472-478. (Pubitemid 36523137)
    • (2003) Chirality , vol.15 , Issue.5 , pp. 472-478
    • Vodicka, P.1    Streinz, L.2    Koutek, B.3    Budesinsky, M.4    Ondracek, J.5    Cisarova, I.6
  • 43
    • 28844464373 scopus 로고    scopus 로고
    • Determining the absolute configuration of secondary alcohols by means of a chiral auxiliary and NOESY
    • DOI 10.1016/j.tetasy.2005.11.003, PII S0957416605008426
    • Domínguez BE, García PE, Cárdenas J,. Determining the absolute configuration of secondary alcohols by means of a chiral auxiliary and NOESY. Tetrahedron: Asymmetry 2005; 16: 3976-3985. (Pubitemid 41773076)
    • (2005) Tetrahedron Asymmetry , vol.16 , Issue.24 , pp. 3976-3985
    • Dominguez, B.E.1    Garcia, P.E.2    Cardenas, J.3
  • 44
    • 0842305159 scopus 로고    scopus 로고
    • Highly efficient chiral resolution and determination of absolute configuration of 2-alkanols by using a cyclopenta[b]furan derivative
    • DOI 10.1016/j.tetlet.2003.12.104
    • Nemoto H, Tsutsumi H, Yuzawa S, Peng X, Zhong W, Xie J, Miyoshi N, Suzuki I, Shibuya M,. Highly efficient chiral resolution and determination of absolute configuration of 2-alkanols by using a cyclopenta[b]furan derivative. Tetrahedron Lett 2004; 45: 1667-1670. (Pubitemid 38169296)
    • (2004) Tetrahedron Letters , vol.45 , Issue.8 , pp. 1667-1670
    • Nemoto, H.1    Tsutsumi, H.2    Yuzawa, S.3    Peng, X.4    Zhong, W.5    Xie, J.6    Miyoshi, N.7    Suzuki, I.8    Shibuya, M.9
  • 45
    • 4544227180 scopus 로고    scopus 로고
    • Chiral silylation reagents: Determining configuration via NMR-spectroscopic coanalysis
    • DOI 10.1021/ol049233b
    • Schroeder FC, Weibel DB, Meinwald J,. Chiral silylation reagents: determining configuration via NMR-spectroscopic coanalysis. Org Lett 2004; 6: 3019-3022. (Pubitemid 39233109)
    • (2004) Organic Letters , vol.6 , Issue.18 , pp. 3019-3022
    • Schroeder, F.C.1    Weibel, D.B.2    Meinwald, J.3
  • 47
    • 37049084867 scopus 로고    scopus 로고
    • Optically active diazacyclophosphamides: Novel efficient reagents for the determination of the absolute configuration of amines and alcohols
    • Oshikawa T, Yamashita M, Kumagai S, Seo K, Kobayashi J,. Optically active diazacyclophosphamides: novel efficient reagents for the determination of the absolute configuration of amines and alcohols. Chem Commun 1995: 435-436.
    • Chem Commun , vol.1995 , pp. 435-436
    • Oshikawa, T.1    Yamashita, M.2    Kumagai, S.3    Seo, K.4    Kobayashi, J.5
  • 48
    • 2942674673 scopus 로고    scopus 로고
    • 31P NMR spectroscopy
    • DOI 10.1016/j.tetasy.2004.04.031, PII S0957416604003131
    • Chauvin A, Bernardinelli G, Alexakis A,. Determination of the absolute configuration of chiral aryl-alkyl carbinols using organophosphorus diamine derivatizing agents by 31P NMR spectroscopy. Tetrahedron: Asymmetry 2004; 15: 1857-1879. (Pubitemid 38780917)
    • (2004) Tetrahedron Asymmetry , vol.15 , Issue.12 , pp. 1857-1879
    • Chauvin, A.-S.1    Bernardinelli, G.2    Alexakis, A.3
  • 49
    • 0000748384 scopus 로고
    • Nonequivalence of the nuclear magnetic resonance spectra of enantiomers in optically active solvents. IV. Assignment of absolute configuration
    • Pirkle WH, Beare SD,. Nonequivalence of the nuclear magnetic resonance spectra of enantiomers in optically active solvents. IV. Assignment of absolute configuration. J Am Chem Soc 1967; 89: 5485-5487.
    • (1967) J Am Chem Soc , vol.89 , pp. 5485-5487
    • Pirkle, W.H.1    Beare, S.D.2
  • 50
    • 0026659841 scopus 로고
    • Optically active trans-bis(hydroxydiphenylmethyl)-2,2-dimethyl-1,3- dioxacyclopentane and its derivatives as chiral shift reagents for the determination of enantiomeric purity and absolute configuration
    • Tanaka K, Ootani M, Toda F,. Optically active trans- bis(hydroxydiphenylmethyl)-2,2-dimethyl-1,3-dioxacyclopentane and its derivatives as chiral shift reagents for the determination of enantiomeric purity and absolute configuration. Tetrahedron: Asymmetry 1992; 3: 709-712.
    • (1992) Tetrahedron: Asymmetry , vol.3 , pp. 709-712
    • Tanaka, K.1    Ootani, M.2    Toda, F.3
  • 51
    • 36549064821 scopus 로고    scopus 로고
    • Trianglamine as a new chiral shift reagent for secondary alcohols
    • DOI 10.1016/j.tetasy.2007.10.024, PII S0957416607007823
    • Tanaka K, Fukuda N, Fujiwara T,. Trianglamine as a new chiral shift reagent for secondary alcohols. Tetrahedron: Asymmetry 2007; 18: 2657-2661. (Pubitemid 350176655)
    • (2007) Tetrahedron Asymmetry , vol.18 , Issue.22 , pp. 2657-2661
    • Tanaka, K.1    Fukuda, N.2    Fujiwara, T.3
  • 52
    • 0242286024 scopus 로고    scopus 로고
    • Application of modified Mosher's method for primary alcohols with a methyl group at C2 position
    • Tsuda M, Toriyabe Y, Endo T, Kobayashi J,. Application of modified Mosher's method for primary alcohols with a methyl group at C2 position. Chem Pharm Bull 2003; 51: 448-451. (Pubitemid 41694826)
    • (2003) Chemical and Pharmaceutical Bulletin , vol.51 , Issue.4 , pp. 448-451
    • Tsuda, M.1    Toriyabe, Y.2    Endo, T.3    Kobayashi, J.4
  • 53
    • 69149096162 scopus 로고    scopus 로고
    • Application of a modified Mosher's method for the determination of enantiomeric ratio and absolute configuration at C-3 of chiral 1,3-dihydroxyketones
    • Galman JL, Hailes HC,. Application of a modified Mosher's method for the determination of enantiomeric ratio and absolute configuration at C-3 of chiral 1,3-dihydroxyketones. Tetrahedron: Asymmetry 2009; 20: 1828-1831.
    • (2009) Tetrahedron: Asymmetry , vol.20 , pp. 1828-1831
    • Galman, J.L.1    Hailes, H.C.2
  • 54
    • 0032550653 scopus 로고    scopus 로고
    • Assignment of the absolute configuration of β-chiral primary alcohols by NMR: Scope and limitations
    • DOI 10.1021/ja972550b
    • Latypov SK, Ferreiro MJ, Quiñoá E, Riguera R,. Assignment of the absolute configuration of β-chiral primary alcohols by NMR: scope and limitations. J Am Chem Soc 1998; 120: 4741-4751. (Pubitemid 28282727)
    • (1998) Journal of the American Chemical Society , vol.120 , Issue.19 , pp. 4741-4751
    • Latypov, S.K.1    Ferreiro, M.J.2    Quinoa, E.3    Riguera, R.4
  • 55
    • 33947669978 scopus 로고    scopus 로고
    • Challenging the absence of observable hydrogens in the assignment of absolute configurations by NMR: Application to chiral primary alcohols
    • DOI 10.1039/b617184b
    • Freire F, Seco JM, Quinoa E, Riguera,. Challenging the absence of observable hydrogens in the assignment of absolute configurations by NMR: application to chiral primary alcohols. Chem Commun 2007: 1456-1458. (Pubitemid 46496520)
    • (2007) Chemical Communications , Issue.14 , pp. 1456-1458
    • Freire, F.1    Seco, J.M.2    Quinoa, E.3    Riguera, R.4
  • 56
    • 0010791095 scopus 로고
    • Use of shift reagent with MTPA derivatives in 1H NMR spectroscopy. III. Determination of absolute configuration and enantiomeric purity of primary carbinols with chiral center at the C-2 Position
    • Yasuhara F, Yamaguchi S,. Use of shift reagent with MTPA derivatives in 1H NMR spectroscopy. III. Determination of absolute configuration and enantiomeric purity of primary carbinols with chiral center at the C-2 Position. Tetrahedron Lett 1977; 18: 4085-4088.
    • (1977) Tetrahedron Lett , vol.18 , pp. 4085-4088
    • Yasuhara, F.1    Yamaguchi, S.2
  • 57
    • 0036521430 scopus 로고    scopus 로고
    • A solution of the "intrinsic problem" of diastereomer method in chiral discrimination. Development of a method for highly efficient and sensitive discrimination of chiral alcohols
    • Ohrui H, Terashima H, Imaizumi K, Akasaka K,. A solution of the "intrinsic problem" of diastereomer method in chiral discrimination. Development of a method for highly efficient and sensitive discrimination of chiral alcohols. Proc Japan Acad Ser B Phys Biol Sci 2002; 78: 69-72.
    • (2002) Proc Japan Acad ser B Phys Biol Sci , vol.78 , pp. 69-72
    • Ohrui, H.1    Terashima, H.2    Imaizumi, K.3    Akasaka, K.4
  • 58
    • 20544473079 scopus 로고    scopus 로고
    • NMR determination of the absolute configuration of β-chiral primary alcohols
    • DOI 10.1016/j.tetlet.2005.05.028, PII S0040403905010245
    • Fukui H, Fukushi Y, Tahara S,. NMR determination of the absolute configuration of β-chiral primary alcohols. Tetrahedron Lett 2005; 46: 5089-5093. (Pubitemid 40840670)
    • (2005) Tetrahedron Letters , vol.46 , Issue.30 , pp. 5089-5093
    • Fukui, H.1    Fukushi, Y.2    Tahara, S.3
  • 59
    • 84986384775 scopus 로고
    • Cath., proceeding with retention of configuration
    • Cath., proceeding with retention of configuration. Helv Chim Acta 1989; 72: 391-400.
    • (1989) Helv Chim Acta , vol.72 , pp. 391-400
    • Fretz, H.1    Woggon, W.2    Voges, R.3
  • 60
    • 0034102478 scopus 로고    scopus 로고
    • Synthesis of allylic isoprenoid diphosphates by SN2 displacement of diethyl phosphate
    • Ravn MM, Jin Q, Coates RM,. Synthesis of allylic isoprenoid diphosphates by SN2 displacement of diethyl phosphate. Eur J Org Chem 2000: 1401-1410.
    • Eur J Org Chem , vol.2000 , pp. 1401-1410
    • Ravn, M.M.1    Jin, Q.2    Coates, R.M.3
  • 61
    • 37049122840 scopus 로고    scopus 로고
    • Determination of the enantiomeric purity and absolute configuration of α-deuteriated primary alcohols
    • Gerlach H, Zagalak B,. Determination of the enantiomeric purity and absolute configuration of α-deuteriated primary alcohols. Chem Commun 1973: 274-275.
    • Chem Commun , vol.1973 , pp. 274-275
    • Gerlach, H.1    Zagalak, B.2
  • 62
    • 0001288832 scopus 로고
    • Identification of absolute configuration of tertiary alcohols by combination of Mosher's method and conformational analysis
    • Izumi S, Moriyoshi H, Hirata T,. Identification of absolute configuration of tertiary alcohols by combination of Mosher's method and conformational analysis. Bull Chem Soc Jpn 1994; 67: 2600-2602.
    • (1994) Bull Chem Soc Jpn , vol.67 , pp. 2600-2602
    • Izumi, S.1    Moriyoshi, H.2    Hirata, T.3
  • 63
    • 59649128088 scopus 로고    scopus 로고
    • Absolute configuration of ketone cyanohydrins by 1H NMR: The special case of polar substituted tertiary alcohols
    • Louzao I, Garcia R, Seco JM, Quinoa E, Riguera R,. Absolute configuration of ketone cyanohydrins by 1H NMR: the special case of polar substituted tertiary alcohols. Org Lett 2009; 11: 53-56.
    • (2009) Org Lett , vol.11 , pp. 53-56
    • Louzao, I.1    Garcia, R.2    Seco, J.M.3    Quinoa, E.4    Riguera, R.5
  • 64
    • 0033235072 scopus 로고    scopus 로고
    • Determination of absolute configurations of tertiary alcohols by NMR spectroscopy
    • Takahashi H, Kato N, Iwashima M, Iguchi K,. Determination of absolute configurations of tertiary alcohols by NMR spectroscopy. Chem Lett 1999; 28: 1181-1182.
    • (1999) Chem Lett , vol.28 , pp. 1181-1182
    • Takahashi, H.1    Kato, N.2    Iwashima, M.3    Iguchi, K.4
  • 65
    • 0032505215 scopus 로고    scopus 로고
    • The fucofuranoside method for determining the absolute configuration of the tertiary alcohols substituted with methyl and two methylene groups
    • PII S0040402098006450
    • Kobayashi M,. The fucofuranoside method for determining the absolute configuration of the tertiary alcohols substituted with methyl and two methylene groups. Tetrahedron 1998; 54: 10987-10998. (Pubitemid 28391990)
    • (1998) Tetrahedron , vol.54 , Issue.37 , pp. 10987-10998
    • Kobayashi, M.1
  • 66
    • 61849146197 scopus 로고    scopus 로고
    • A new chiral shift reagent for the determination of enantiomeric excess and absolute configuration in cyanohydrins
    • Moon LS, Jolly RS, Kasetti Y, Bharatam PV,. A new chiral shift reagent for the determination of enantiomeric excess and absolute configuration in cyanohydrins. Chem Commun 2009: 1067-1069.
    • Chem Commun , vol.2009 , pp. 1067-1069
    • Moon, L.S.1    Jolly, R.S.2    Kasetti, Y.3    Bharatam, P.V.4
  • 67
    • 0042335750 scopus 로고    scopus 로고
    • Application of chiral bidentate NMR solvents for assignment of the absolute configuration of alcohols: Scope and limitation
    • DOI 10.1016/j.tetlet.2003.08.022
    • Kobayashi Y, Hayashi N, Kishi Y,. Application of chiral bidentate NMR solvents for assignment of the absolute configuration of alcohols: scope and limitation. Tetrahedron Lett 2003; 44: 7489-7491. (Pubitemid 37102984)
    • (2003) Tetrahedron Letters , vol.44 , Issue.40 , pp. 7489-7491
    • Kobayashi, Y.1    Hayashi, N.2    Kishi, Y.3
  • 68
    • 0007102419 scopus 로고    scopus 로고
    • Application of the modified Mosher's method to acyclic glycols
    • Ichikawa A,. Application of the modified Mosher's method to acyclic glycols. Enantiomer 1997; 2: 327-331. (Pubitemid 127716127)
    • (1997) Enantiomer , vol.2 , Issue.5 , pp. 327-331
    • Ichikawa, A.1
  • 69
    • 0031795721 scopus 로고    scopus 로고
    • Application of the modified Mosher's method to acyclic glycols (2). Glycols possessing aromatic groups
    • Ichikawa A,. Application of the modified Mosher's method to acyclic glycols 2. Glycols possessing aromatic groups. Enantiomer 1998; 3: 255-261. (Pubitemid 28517614)
    • (1998) Enantiomer , vol.3 , Issue.3 , pp. 255-261
    • Ichikawa, A.1
  • 70
    • 25444502911 scopus 로고    scopus 로고
    • 1H NMR spectroscopy: Principles and applications
    • DOI 10.1002/chem.200500181
    • Freire F, Seco JM, Quiñoá E, Riguera R,. The prediction of the absolute stereochemistry of primary and secondary 1,2-diols by 1H NMR spectroscopy: principles and applications. Chem Eur J 2005; 11: 5509-5522. (Pubitemid 41368729)
    • (2005) Chemistry - A European Journal , vol.11 , Issue.19 , pp. 5509-5522
    • Freire, F.1    Seco, J.M.2    Quinoa, E.3    Riguera, R.4
  • 71
    • 18744369934 scopus 로고    scopus 로고
    • 1H NMR: Basis and applications
    • DOI 10.1021/jo048643a
    • Freire F, Seco JM, Quiñoá E, Riguera R,. Determining the absolute stereochemistry of secondary/secondary diols by 1H NMR: basis and applications. J Org Chem 2005; 70: 3778-3790. (Pubitemid 40675303)
    • (2005) Journal of Organic Chemistry , vol.70 , Issue.10 , pp. 3778-3790
    • Freire, F.1    Seco, J.M.2    Quinoa, E.3    Riguera, R.4
  • 73
    • 74949112163 scopus 로고    scopus 로고
    • Chiral 1,2-diols: The assignment of their absolute configuration by NMR made easy
    • Freire F, Seco JM, Quinoa E, Riguera R,. Chiral 1,2-diols: the assignment of their absolute configuration by NMR made easy. Org Lett 2010; 12: 208-211.
    • (2010) Org Lett , vol.12 , pp. 208-211
    • Freire, F.1    Seco, J.M.2    Quinoa, E.3    Riguera, R.4
  • 74
    • 0036135410 scopus 로고    scopus 로고
    • Determination of absolute configuration of 1,3-diols by the modified Mosher's method using their di-MTPA esters
    • DOI 10.1002/chir.10035
    • Konno K, Fujishima T, Liu Z, Takayama H,. Determination of absolute configuration of 1,3-diols by the modified Mosher's method using their di-MTPA esters. Chirality 2002; 13: 72-80. (Pubitemid 34024604)
    • (2002) Chirality , vol.14 , Issue.1 , pp. 72-80
    • Konno, K.1    Fujishima, T.2    Liu, Z.3    Takayama, H.4
  • 75
    • 0001290748 scopus 로고
    • A CD method for determination of the absolute stereochemistry of acyclic glycols. 1. Application of the CD exciton chirality method to acyclic 1,3-dibenzoate systems
    • Harada N, Saito A, Ono H, Gawronski J, Gawronska K, Sugioka T, Uda H, Kuriki T,. A CD method for determination of the absolute stereochemistry of acyclic glycols. 1. Application of the CD exciton chirality method to acyclic 1,3-dibenzoate systems. J Am Chem Soc 1991; 113: 3842-3850.
    • (1991) J Am Chem Soc , vol.113 , pp. 3842-3850
    • Harada, N.1    Saito, A.2    Ono, H.3    Gawronski, J.4    Gawronska, K.5    Sugioka, T.6    Uda, H.7    Kuriki, T.8
  • 76
    • 72949083166 scopus 로고    scopus 로고
    • The stereochemistry of 1,2,3-triols revealed by 1H NMR spectroscopy: Principles and applications
    • Freire F, Lallana E, Quinoa E, Riguera R,. The stereochemistry of 1,2,3-triols revealed by 1H NMR spectroscopy: principles and applications. Chem Eur J 2009; 15: 11963-11975.
    • (2009) Chem Eur J , vol.15 , pp. 11963-11975
    • Freire, F.1    Lallana, E.2    Quinoa, E.3    Riguera, R.4
  • 77
    • 8444223084 scopus 로고    scopus 로고
    • Assignment of the relative and absolute configurations of acyclic secondary 1,2-diols
    • DOI 10.1016/j.tet.2004.08.101, PII S0040402004015042
    • Higashibayashi S, Kishi Y,. Assignment of the relative and absolute configurations of acyclic secondary 1,2-diols. Tetrahedron 2004; 60: 11977-11982. (Pubitemid 39487447)
    • (2004) Tetrahedron , vol.60 , Issue.51 , pp. 11977-11982
    • Higashibayashi, S.1    Kishi, Y.2
  • 78
    • 0035850292 scopus 로고    scopus 로고
    • Toward the creation of NMR databases in chiral solvents for assignments of relative and absolute stereochemistry: Proof of concept
    • DOI 10.1021/ol010108z
    • Kobayashi Y, Hayashi N, Tan C, Kishi Y,. Toward the creation of NMR databases in chiral solvents for assignments of relative and absolute stereochemistry: proof of concept. Org Lett 2001; 3: 2245-2248. (Pubitemid 33627139)
    • (2001) Organic Letters , vol.3 , Issue.14 , pp. 2245-2248
    • Kobayashi, Y.1    Hayashi, N.2    Tan, C.-H.3    Kishi, Y.4
  • 79
    • 0033619844 scopus 로고    scopus 로고
    • Toward creation of a universal NMR database for the stereochemical assignment of acyclic compounds: The case of two contiguous propionate units
    • Kobayashi Y, Lee J, Tezuka K, Kishi Y,. Toward creation of a universal NMR database for the stereochemical assignment of acyclic compounds: the case of two contiguous propionate units. Org Lett 1999; 1: 2177-2180.
    • (1999) Org Lett , vol.1 , pp. 2177-2180
    • Kobayashi, Y.1    Lee, J.2    Tezuka, K.3    Kishi, Y.4
  • 80
    • 70349772081 scopus 로고    scopus 로고
    • Advances in the universal NMR database: Toward the determination of the relative configurations of large polypropionates
    • Fleury E, Lannou MI, Bistri O, Sautel F, Massiot G, Pancrazi A, Ardisson J,. Advances in the universal NMR database: toward the determination of the relative configurations of large polypropionates. Eur J Org Chem 2009: 4992-5001.
    • Eur J Org Chem , vol.2009 , pp. 4992-5001
    • Fleury, E.1    Lannou, M.I.2    Bistri, O.3    Sautel, F.4    Massiot, G.5    Pancrazi, A.6    Ardisson, J.7
  • 81
    • 70349146708 scopus 로고    scopus 로고
    • Pattern-based recognition for the rapid determination of identity, concentration, and enantiomeric excess of subtly different threo diols
    • Shabbir SH, Joyce LA, da Cruz GM, Lynch VM, Sorey S, Anslyn EV,. Pattern-based recognition for the rapid determination of identity, concentration, and enantiomeric excess of subtly different threo diols. J Am Chem Soc 2009; 131: 13125-13131.
    • (2009) J Am Chem Soc , vol.131 , pp. 13125-13131
    • Shabbir, S.H.1    Joyce, L.A.2    Da Cruz, G.M.3    Lynch, V.M.4    Sorey, S.5    Anslyn, E.V.6
  • 82
    • 0342423948 scopus 로고
    • Assignment of absolute configuration to metabolically formed trans-dihydrodiols of dibenz[a,h]anthracene by two distinct spectroscopic methods
    • Schollmeier M, Frank H, Oesch F, Platt KL,. Assignment of absolute configuration to metabolically formed trans-dihydrodiols of dibenz[a,h] anthracene by two distinct spectroscopic methods. J Org Chem 1986; 51: 5368-5372.
    • (1986) J Org Chem , vol.51 , pp. 5368-5372
    • Schollmeier, M.1    Frank, H.2    Oesch, F.3    Platt, K.L.4
  • 83
    • 0002915314 scopus 로고
    • Synthesis of enantiomerically pure bay-region 3,4-diol 1,2-epoxide diastereomers and other derivatives of the potent carcinogen dibenz[c,h] acridine
    • Lehr RE, Kumar S, Shirai N, Jerina DM,. Synthesis of enantiomerically pure bay-region 3,4-diol 1,2-epoxide diastereomers and other derivatives of the potent carcinogen dibenz[c,h] acridine. J Org Chem 1985; 50: 98-107.
    • (1985) J Org Chem , vol.50 , pp. 98-107
    • Lehr, R.E.1    Kumar, S.2    Shirai, N.3    Jerina, D.M.4
  • 84
    • 0034677827 scopus 로고    scopus 로고
    • 13C NMR method for determining the absolute configuration of the 1,2-glycols consisting of secondary and tertiary hydroxyl groups
    • DOI 10.1016/S0040-4020(00)00070-3, PII S0040402000000703
    • Kobayashi M,. The 13C NMR method for determining the absolute configuration of the 1,2-glycols consisting of secondary and tertiary hydroxyl groups. Tetrahedron 2000; 56: 1661-1665. (Pubitemid 30190433)
    • (2000) Tetrahedron , vol.56 , Issue.12 , pp. 1661-1665
    • Kobayashi, M.1
  • 85
    • 0038327829 scopus 로고    scopus 로고
    • NMR determination of the absolute configuration of chiral 1,2- and 1,3-diols
    • DOI 10.1016/S0040-4039(03)00845-1
    • Fukui H, Fukushi Y, Tahara S,. NMR determination of the absolute configuration of chiral 1,2- and 1,3-diols. Tetrahedron Lett 2003; 44: 4063-4065. (Pubitemid 36549130)
    • (2003) Tetrahedron Letters , vol.44 , Issue.21 , pp. 4063-4065
    • Fukui, H.1    Fukushi, Y.2    Tahara, S.3
  • 86
    • 0000031605 scopus 로고
    • Stereoselective acetalization of 1,3-alkanediols by L-menthone: Application to the resolution of racemic 1,3-alkanediols and to the determination of the absolute configuration of enantiomeric 1,3-alkanediols
    • Harada T, Kurokawa H, Kagamihara Y, Tanaka S, Inoue A, Oku A,. Stereoselective acetalization of 1,3-alkanediols by L-menthone: application to the resolution of racemic 1,3-alkanediols and to the determination of the absolute configuration of enantiomeric 1,3-alkanediols. J Org Chem 1992; 57: 1412-1421.
    • (1992) J Org Chem , vol.57 , pp. 1412-1421
    • Harada, T.1    Kurokawa, H.2    Kagamihara, Y.3    Tanaka, S.4    Inoue, A.5    Oku, A.6
  • 87
    • 0001224353 scopus 로고    scopus 로고
    • Carbon-13 NMR study of the stereoisomerism of 4,5-disubstituted 2,2-dimethyl-1,3-dioxolanes
    • Dana G, Danechpajouh H,. Carbon-13 NMR study of the stereoisomerism of 4,5-disubstituted 2,2-dimethyl-1,3-dioxolanes. Bull Soc Chim Fr 1980: 395-399.
    • Bull Soc Chim Fr , vol.1980 , pp. 395-399
    • Dana, G.1    Danechpajouh, H.2
  • 88
    • 0013519976 scopus 로고
    • Synthesis and absolute configuration of two diastereoisomeric (1R, 2S, 3R)- and (1S, 2S, 3R)-2-amino-1-(2-furyl)-1,3-butandiols
    • Szechner B,. Synthesis and absolute configuration of two diastereoisomeric (1R, 2S, 3R)- and (1S, 2S, 3R)-2-amino-1-(2-furyl)-1,3- butandiols. Tetrahedron 1981; 37: 949-952.
    • (1981) Tetrahedron , vol.37 , pp. 949-952
    • Szechner, B.1
  • 89
    • 0029000548 scopus 로고
    • Chemoenzymatic synthesis of chiral boronates for the 1H NMR determination of the absolute configuration and enantiomeric excess of bacterial and synthetic cis-diols
    • Resnick SM, Torok DS, Gibson DT,. Chemoenzymatic synthesis of chiral boronates for the 1H NMR determination of the absolute configuration and enantiomeric excess of bacterial and synthetic cis-diols. J Org Chem 1995; 60: 3546-3549.
    • (1995) J Org Chem , vol.60 , pp. 3546-3549
    • Resnick, S.M.1    Torok, D.S.2    Gibson, D.T.3
  • 90
    • 0011249494 scopus 로고
    • Use of osmate(VI) ester trans-N,N,N',N'-tetramethyl-1,2- cyclohexanediamine complexes for determination of glycol stereochemistry
    • Resch JF, Meinwald J,. Use of osmate(VI) ester trans-N,N,N',N'- tetramethyl-1,2-cyclohexanediamine complexes for determination of glycol stereochemistry. Tetrahedron Lett 1981; 22: 3159-3162.
    • (1981) Tetrahedron Lett , vol.22 , pp. 3159-3162
    • Resch, J.F.1    Meinwald, J.2
  • 91
    • 0030953273 scopus 로고    scopus 로고
    • 1H NMR spectroscopy of their per-O-(S)-2-methylbutyrate derivatives
    • DOI 10.1016/S0008-6215(97)00050-5, PII S0008621597000505
    • York WS, Hantus S, Albersheim P, Darvill AG,. Determination of the absolute configuration of monosaccharides by 1H NMR spectroscopy of their per-O-(S)-2-methylbutyrate derivatives. Carbohydr Res 1997; 300: 199-206. (Pubitemid 27217815)
    • (1997) Carbohydrate Research , vol.300 , Issue.3 , pp. 199-206
    • York, W.S.1    Hantus, S.2    Albersheim, P.3    Darvill, A.G.4
  • 92
    • 0032453988 scopus 로고    scopus 로고
    • Synthesis and NMR studies of methyl 3-O-[(R)- and (S)-1-carboxyethyl]- α-D-gluco-, galacto- and manno- pyranosides
    • DOI 10.1016/S0008-6215(98)00272-9, PII S0008621598002729
    • Andersson L, Kenne L,. Synthesis and NMR studies of methyl 3-O-[(R)- and (S)-1-carboxyethyl]-α-D-gluco-, galacto- and manno-pyranosides. Carbohydr Res 1998; 313: 157-164. (Pubitemid 29129508)
    • (1998) Carbohydrate Research , vol.313 , Issue.3-4 , pp. 157-164
    • Andersson, L.1    Kenne, L.2
  • 93
    • 0026228555 scopus 로고
    • Determination of the absolute configuration of monosaccharides using (+) or (-) 2-tert-butyl-2-methyl-1,3-benzodioxole-4-carboxylic acid and high-resolution 1H-NMR spectroscopy
    • Nishida Y, Kumagai M, Kamiyama A, Ohrui H, Meguro H,. Determination of the absolute configuration of monosaccharides using (+) or (-) 2-tert-butyl-2-methyl-1,3-benzodioxole-4-carboxylic acid and high-resolution 1H-NMR spectroscopy. Carbohydr Res 1991; 218: 63-73.
    • (1991) Carbohydr Res , vol.218 , pp. 63-73
    • Nishida, Y.1    Kumagai, M.2    Kamiyama, A.3    Ohrui, H.4    Meguro, H.5
  • 94
    • 0036400758 scopus 로고    scopus 로고
    • Determination of the D- and L-configurations of amino deoxy sugars by (S)-TBMB carboxylic acid, a fluorescent chiral derivatization reagent
    • Bai C, Liang B, Wang S, Zheng X, Lin Z, Huang W,. Determination of the D- and L-configurations of amino deoxy sugars by (S)-TBMB carboxylic acid, a fluorescent chiral derivatization reagent. Shengwu Huaxue Yu Shengwu Wuli Xuebao 2002; 34: 615-618. (Pubitemid 35193145)
    • (2002) Acta Biochimica et Biophysica Sinica , vol.34 , Issue.5 , pp. 615-618
    • Bai, C.1    Liang, B.2    Wang, S.-Z.3    Zheng, X.-X.4    Lin, Z.-P.5    Huang, W.-D.6
  • 95
    • 0342714457 scopus 로고
    • Determination of the absolute and anomeric configurations of sugars in oligo- and polysaccharides by the effect of glycosylation in carbon-13 NMR spectra
    • Shashkov AS, Usov AI, Knirel YA, Dmitriev BA, Kochetkov NK,. Determination of the absolute and anomeric configurations of sugars in oligo- and polysaccharides by the effect of glycosylation in carbon-13 NMR spectra. Russ J Bioorg Chem 1981; 7: 1364-1371.
    • (1981) Russ J Bioorg Chem , vol.7 , pp. 1364-1371
    • Shashkov, A.S.1    Usov, A.I.2    Knirel, Y.A.3    Dmitriev, B.A.4    Kochetkov, N.K.5
  • 97
    • 1542701400 scopus 로고
    • Determination of the Absolute Configuration and the Conformation of Carbohydrate Molecules Based on the Approach of Analytical Organic Chemistry
    • Nishida Y,. Determination of the absolute configuration and the conformation of carbohydrate molecules based on the approach of analytical organic chemistry. Tohoku J Agric Res 1995; 46: 73-91. (Pubitemid 126029313)
    • (1995) TOHOKU JOURNAL OF AGRICULTURAL RESEARCH , vol.46 , Issue.1-2 , pp. 73-91
    • Nishida, Y.1
  • 98
    • 0027051086 scopus 로고
    • 13C NMR data
    • DOI 10.1016/S0008-6215(92)84229-L
    • Lipkind GM, Shashkov AS, Nifant'ev NE, Kochetkov NK,. Computer-assisted analysis of the structure of regular branched polysaccharides containing 2,3-disubstituted rhamnopyranose and mannopyranose residues on the basis of 13C NMR data. Carbohydr Res 1992; 237: 11-22. (Pubitemid 23021091)
    • (1992) Carbohydrate Research , vol.237 , pp. 11-22
    • Lipkind, G.M.1    Shashkov, A.S.2    Nifant'ev, N.E.3    Kochetkov, N.K.4
  • 99
    • 0034723380 scopus 로고    scopus 로고
    • Phenylglycine methyl ester, a useful tool for absolute configuration determination of various chiral carboxylic acids
    • DOI 10.1021/jo991218a
    • Yabuuchi T, Kusumi T,. Phenylglycine methyl ester, a useful tool for absolute configuration determination of various chiral carboxylic acids. J Org Chem 2000; 65: 397-404. (Pubitemid 30061118)
    • (2000) Journal of Organic Chemistry , vol.65 , Issue.2 , pp. 397-404
    • Yabuuchi, T.1    Kusumi, T.2
  • 100
    • 0001908387 scopus 로고    scopus 로고
    • Determination of the absolute configuration of biologically active compounds by the modified Mosher's method
    • Kusumi T, Ohtani II,. Determination of the absolute configuration of biologically active compounds by the modified Mosher's method. Biol-Chem Interface 1999: 103-137.
    • Biol-Chem Interface , vol.1999 , pp. 103-137
    • Kusumi, T.1    Ohtani, I.I.2
  • 101
    • 18944403941 scopus 로고    scopus 로고
    • Objective separation and absolute configuration of enantiomeric carboxylic acids and amines. 1
    • Helmchen G, Ott R, Sauber K,. Objective separation and absolute configuration of enantiomeric carboxylic acids and amines. 1. Tetrahedron Lett 1972: 3873-3878.
    • Tetrahedron Lett , vol.1972 , pp. 3873-3878
    • Helmchen, G.1    Ott, R.2    Sauber, K.3
  • 102
    • 0034175635 scopus 로고    scopus 로고
    • An NMR method for determination of configuration of β-substituted carboxylic acids
    • DOI 10.1016/S0040-4039(00)00163-5, PII S0040403900001635
    • Hoye TR, Hamad AS, Koltun DO, Tennakoon MA,. An NMR method for determination of configuration of β-substituted carboxylic acids. Tetrahedron Lett 2000; 41: 2289-2293. (Pubitemid 30217047)
    • (2000) Tetrahedron Letters , vol.41 , Issue.14 , pp. 2289-2293
    • Hoye, T.R.1    Hamad, A.-S.S.2    Koltun, D.O.3    Tennakoon, M.A.4
  • 104
    • 0035260993 scopus 로고    scopus 로고
    • Synthesis, absolute configuration and biological activity of both enantiomers of 2-(5,6-dichloro-3-indolyl)propionic acid: New dichloroindole auxins
    • DOI 10.1271/bbb.65.270
    • Katayama M, Kato Y, Marumo S,. Synthesis, absolute configuration and biological activity of both enantiomers of 2-(5,6-dichloro-3-indolyl)propionic acid: new dichloroindole auxins. Biosci Biotechnol Biochem 2001; 65: 270-276. (Pubitemid 33626236)
    • (2001) Bioscience, Biotechnology and Biochemistry , vol.65 , Issue.2 , pp. 270-276
    • Katayama, M.1    Kato, Y.2    Marumo, S.3
  • 105
    • 4544233004 scopus 로고    scopus 로고
    • Synthesis, absolute configuration and biological activities of both enantiomers of 2-(5,7-dichloro-3-indolyl)propionic acid: A novel dichloroindole auxin and antiauxin
    • DOI 10.1271/bbb.68.1287
    • Katayama M, Kato Y, Marumo S,. Synthesis, absolute configuration and biological activities of both enantiomers of 2-(5,7-dichloro-3-indolyl)propionic acid: a novel dichloroindole auxin and antiauxin. Biosci Biotechnol Biochem 2004; 68: 1287-1292. (Pubitemid 39251386)
    • (2004) Bioscience, Biotechnology and Biochemistry , vol.68 , Issue.6 , pp. 1287-1292
    • Katayama, M.1    Kato, Y.2    Marumo, S.3
  • 106
    • 0028048654 scopus 로고
    • Stereoisomeric flavour compounds LXVII. 2-, 3-, and 4-alkyl-branched acids, part 1: General approach to the synthesis of the enantiopure acids
    • Karl V, Kaunzinger A, Gutser J, Steuer P, Angles-Angel J, Mosandl A,. Stereoisomeric flavour compounds LXVII. 2-, 3-, and 4-Alkyl-branched acids, part 1: general approach to the synthesis of the enantiopure acids. Chirality 1994; 6: 420-426. (Pubitemid 24273951)
    • (1994) Chirality , vol.6 , Issue.5 , pp. 420-426
    • Karl, V.1    Kaunzinger, A.2    Gutser, J.3    Steuer, P.4    Angles-Angel, J.5    Mosandl, A.6
  • 108
    • 62849122560 scopus 로고    scopus 로고
    • Synthesis of optically active α-benzyl paraconic acids and their esters and assignment of their absolute configuration
    • Berti F, Forzato C, Furlan G, Nitti P, Pitacco G, Valentin E, Zangrando E,. Synthesis of optically active α-benzyl paraconic acids and their esters and assignment of their absolute configuration. Tetrahedron: Asymmetry 2009; 20: 313-321.
    • (2009) Tetrahedron: Asymmetry , vol.20 , pp. 313-321
    • Berti, F.1    Forzato, C.2    Furlan, G.3    Nitti, P.4    Pitacco, G.5    Valentin, E.6    Zangrando, E.7
  • 109
    • 33749259049 scopus 로고    scopus 로고
    • Chemoenzymatic synthesis of diastereomeric ethyl γ-benzyl paraconates and determination of the absolute configurations of their acids
    • DOI 10.1016/j.tetasy.2006.08.013, PII S0957416606006215
    • Berti F, Felluga F, Forzato C, Furlan G, Nitti P, Pitacco G, Valentin E,. Chemoenzymatic synthesis of diastereomeric ethyl α-benzyl paraconates and determination of the absolute configurations of their acids. Tetrahedron: Asymmetry 2006; 17: 2344-2353. (Pubitemid 44485502)
    • (2006) Tetrahedron Asymmetry , vol.17 , Issue.16 , pp. 2344-2353
    • Berti, F.1    Felluga, F.2    Forzato, C.3    Furlan, G.4    Nitti, P.5    Pitacco, G.6    Valentin, E.7
  • 110
    • 0030586223 scopus 로고    scopus 로고
    • 1H nuclear magnetic resonance spectroscopy for the determination of the absolute configuration of chiral carboxylic acids
    • DOI 10.1016/0040-4020(96)00516-9
    • Tyrrell E, Tsang MWH, Skinner GA, Fawcett J,. The application of 1H nuclear magnetic resonance spectroscopy for the determination of the absolute configuration of chiral carboxylic acids. Tetrahedron 1996; 52: 9841-9852. (Pubitemid 26267197)
    • (1996) Tetrahedron , vol.52 , Issue.29 , pp. 9841-9852
    • Tyrrell, E.1    Tsang, M.W.H.2    Skinner, G.A.3    Fawcett, J.4
  • 111
    • 0030200525 scopus 로고    scopus 로고
    • A new NMR chiral derivatizing reagent for determining the absolute configurations of carboxylic acids
    • DOI 10.1016/0040-4039(96)00954-9
    • Fukushi Y, Shigematsu K, Mizutani J, Tahara S,. A new NMR chiral derivatizing reagent for determining the absolute configurations of carboxylic acids. Tetrahedron Lett 1996; 37: 4737-4740. (Pubitemid 26225570)
    • (1996) Tetrahedron Letters , vol.37 , Issue.27 , pp. 4737-4740
    • Fukushi, Y.1    Shigematsu, K.2    Mizutani, J.3    Tahara, S.4
  • 112
    • 37049087887 scopus 로고    scopus 로고
    • 1,2-Diphenylethane-1,2-diamine: An effective NMR chiral solvating agent for chiral carboxylic acids
    • Fulwood R, Parker D,. 1,2-Diphenylethane-1,2-diamine: an effective NMR chiral solvating agent for chiral carboxylic acids. J Chem Soc, Perkin Trans 2 1994: 57-64.
    • J Chem Soc, Perkin Trans 2 , vol.1994 , pp. 57-64
    • Fulwood, R.1    Parker, D.2
  • 113
    • 3242754320 scopus 로고    scopus 로고
    • 1H-NMR
    • Murray RS, Boyd VA, Lynch VM, Negrete GR,. Pyrimidinone conjugate for the assignment of the absolute configuration of α-chiral carboxylic acids by 1H-NMR. ARKIVOC 2001; 2001: 58-73. (Pubitemid 38972338)
    • (2001) Arkivoc , vol.2001 , Issue.11 , pp. 58-73
    • Murray, R.S.1    Boyd, V.A.2    Lynch, V.M.3    Negrete, G.R.4
  • 114
    • 52049084094 scopus 로고    scopus 로고
    • In tube determination of the absolute configuration of α- And β-hydroxy acids by NMR via chiral BINOL borates
    • Friere F, Quinoa E, Riguera R,. In tube determination of the absolute configuration of α- and β-hydroxy acids by NMR via chiral BINOL borates. Chem Commun 2008: 4147-4149.
    • Chem Commun , vol.2008 , pp. 4147-4149
    • Friere, F.1    Quinoa, E.2    Riguera, R.3
  • 115
    • 34250719114 scopus 로고    scopus 로고
    • Structurally simple chiral thioureas as chiral solvating agents in the enantiodiscrimination of α-hydroxy and α-amino carboxylic acids
    • DOI 10.1016/j.tet.2007.05.021, PII S0040402007008514
    • Hernandez-Rodriguez M, Juaristi E,. Structurally simple chiral thioureas as chiral solvating agents in the enantiodiscrimination of α-hydroxy and β-amino carboxylic acids. Tetrahedron 2007; 63: 7673-7678. (Pubitemid 46962639)
    • (2007) Tetrahedron , vol.63 , Issue.32 , pp. 7673-7678
    • Hernandez-Rodriguez, M.1    Juaristi, E.2
  • 116
    • 61549123666 scopus 로고    scopus 로고
    • 'Calixarene-like' chiral amine macrocycles as novel chiral shift reagents for carboxylic acids
    • Tanaka K, Fukuda N,. 'Calixarene-like' chiral amine macrocycles as novel chiral shift reagents for carboxylic acids. Tetrahedron: Asymmetry 2009; 20: 111-114.
    • (2009) Tetrahedron: Asymmetry , vol.20 , pp. 111-114
    • Tanaka, K.1    Fukuda, N.2
  • 117
    • 65649144745 scopus 로고    scopus 로고
    • Absolute configuration of ceriporic acids, the iron redox-silencing metabolites produced by a selective lignin-degrading fungus, Ceriporiopsis subvermispora
    • Nishimura H, Murayama K, Watanabe T, Honda Y, Watanabe T,. Absolute configuration of ceriporic acids, the iron redox-silencing metabolites produced by a selective lignin-degrading fungus, Ceriporiopsis subvermispora. Chem Phys Lipids 2009; 159: 77-80.
    • (2009) Chem Phys Lipids , vol.159 , pp. 77-80
    • Nishimura, H.1    Murayama, K.2    Watanabe, T.3    Honda, Y.4    Watanabe, T.5
  • 118
    • 0026466088 scopus 로고
    • Absolute configuration of aldonic acids and lanthanoid induced shift by the chiral shift reagent propylenediaminetetraacetatoeuropium(III) in aqueous solution
    • Kabuto K, Sasaki K, Sasaki Y,. Absolute configuration of aldonic acids and lanthanoid induced shift by the chiral shift reagent propylenediaminetetraacetatoeuropium(III) in aqueous solution. Tetrahedron: Asymmetry 1992; 3: 1357-1360.
    • (1992) Tetrahedron: Asymmetry , vol.3 , pp. 1357-1360
    • Kabuto, K.1    Sasaki, K.2    Sasaki, Y.3
  • 119
    • 0016932097 scopus 로고
    • Determination of enantiomeric purity of glycerides with a chiral PMR shift reagent
    • Bus J, Lok CM, Groenewegen A,. Determination of enantiomeric purity of glycerides with a chiral PMR shift reagent. Chem Phys Lipids 1976; 16: 123-132.
    • (1976) Chem Phys Lipids , vol.16 , pp. 123-132
    • Bus, J.1    Lok, C.M.2    Groenewegen, A.3
  • 120
    • 2242449835 scopus 로고
    • Experiments directed towards the synthesis of anthracyclinones. XXIV. Homochiral intermediates for vineomycin syntheses
    • Pausler MG, Rutledge PS,. Experiments directed towards the synthesis of anthracyclinones. XXIV. Homochiral intermediates for vineomycin syntheses. Aust J Chem 1994; 47: 2149-2160.
    • (1994) Aust J Chem , vol.47 , pp. 2149-2160
    • Pausler, M.G.1    Rutledge, P.S.2
  • 121
    • 33748618450 scopus 로고    scopus 로고
    • Attempts to assemble a universal NMR database without synthesis of NMR database compounds
    • DOI 10.1021/ol061580t
    • Seike H, Ghosh I, Kishi Y,. Attempts to assemble a universal NMR database without synthesis of NMR database compounds. Org Lett 2006; 8: 3861-3864. (Pubitemid 44378382)
    • (2006) Organic Letters , vol.8 , Issue.17 , pp. 3861-3864
    • Seike, H.1    Ghosh, I.2    Kishi, Y.3
  • 122
    • 0034605919 scopus 로고    scopus 로고
    • Stereochemical assignment of the C21-C38 portion of the desertomycin/oasomycin class of natural products by using universal NMR databases: Prediction
    • Kobayashi Y, Tan C, Kishi Y,. Stereochemical assignment of the C21-C38 portion of the desertomycin/oasomycin class of natural products by using universal NMR databases: prediction. Angew Chem, Int Ed 2000; 39: 4279-4281.
    • (2000) Angew Chem, Int Ed , vol.39 , pp. 4279-4281
    • Kobayashi, Y.1    Tan, C.2    Kishi, Y.3
  • 123
    • 0035819982 scopus 로고    scopus 로고
    • Toward creation of a universal NMR database for stereochemical assignment: Complete structure of the desertomycin/oasomycin class of natural products [10]
    • DOI 10.1021/ja004154q
    • Kobayashi Y, Tan C, Kishi Y,. Toward creation of a universal NMR database for stereochemical assignment: complete structure of the desertomycin/oasomycin class of natural products. J Am Chem Soc 2001; 123: 2076-2078. (Pubitemid 32200037)
    • (2001) Journal of the American Chemical Society , vol.123 , Issue.9 , pp. 2076-2078
    • Kobayashi, Y.1    Tan, C.-H.2    Kishi, Y.3
  • 124
    • 33847088636 scopus 로고
    • Nuclear magnetic resonance determination of enantiomeric composition and absolute configuration of γ-lactones using chiral 2,2,2-trifluoro-1-(9- anthryl)ethanol
    • Pirkle WH, Sikkenga DL, Pavlin MS,. Nuclear magnetic resonance determination of enantiomeric composition and absolute configuration of γ-lactones using chiral 2,2,2-trifluoro-1-(9-anthryl)ethanol. J Org Chem 1977; 42: 384-387.
    • (1977) J Org Chem , vol.42 , pp. 384-387
    • Pirkle, W.H.1    Sikkenga, D.L.2    Pavlin, M.S.3
  • 125
    • 0000170052 scopus 로고
    • The use of chiral solvating agents for nuclear magnetic resonance determination of enantiomeric purity and absolute configuration of lactones. Consequences of three-point interactions
    • Pirkle WH, Sikkenga DL,. The use of chiral solvating agents for nuclear magnetic resonance determination of enantiomeric purity and absolute configuration of lactones. Consequences of three-point interactions. J Org Chem 1977; 42: 1370-1374.
    • (1977) J Org Chem , vol.42 , pp. 1370-1374
    • Pirkle, W.H.1    Sikkenga, D.L.2
  • 126
    • 18844400147 scopus 로고
    • Determination of enantiomeric purity and absolute configuration of chiral β-propiolactones by nuclear magnetic resonance in optically active solvents
    • Leborgne A, Moreau M, Spassky N,. Determination of enantiomeric purity and absolute configuration of chiral β-propiolactones by nuclear magnetic resonance in optically active solvents. Tetrahedron Lett 1983; 24: 1027-1030.
    • (1983) Tetrahedron Lett , vol.24 , pp. 1027-1030
    • Leborgne, A.1    Moreau, M.2    Spassky, N.3
  • 127
    • 0001622565 scopus 로고
    • Enantiomerically pure lactones. 3. Synthesis of and stereospecific conjugate additions to α,β-unsaturated lactones
    • Pirkle WH, Adams PE,. Enantiomerically pure lactones. 3. Synthesis of and stereospecific conjugate additions to α,β-unsaturated lactones. JOrg Chem 1980; 45: 4117-4121.
    • (1980) JOrg Chem , vol.45 , pp. 4117-4121
    • Pirkle, W.H.1    Adams, P.E.2
  • 128
    • 33751391368 scopus 로고
    • Degradation and absolute configurational assignment to C34-botryococcene
    • White JD, Somers TC, Reddy GN,. Degradation and absolute configurational assignment to C34-botryococcene. J Org Chem 1992; 57: 4991-4998.
    • (1992) J Org Chem , vol.57 , pp. 4991-4998
    • White, J.D.1    Somers, T.C.2    Reddy, G.N.3
  • 129
    • 0005239672 scopus 로고
    • Synthesis and separation of diastereomeric imino alcohol derivatives of chiral phthalides: A method for assignment of phthalide absolute configurations
    • Pirkle WH, Sowin TJ,. Synthesis and separation of diastereomeric imino alcohol derivatives of chiral phthalides: a method for assignment of phthalide absolute configurations. J Org Chem 1987; 52: 3011-3017.
    • (1987) J Org Chem , vol.52 , pp. 3011-3017
    • Pirkle, W.H.1    Sowin, T.J.2
  • 131
    • 0028288492 scopus 로고
    • (N-Methylphenylsulfoximidoyl)methyllithium: A versatile reagent for the determination of absolute configuration of six-membered ring ketones
    • DOI 10.1016/0957-4166(94)80003-0
    • Preite MD, González-Sierra M, Zinczuk J, Rúveda EA,. (N-Methylphenylsulfoximidoyl)methyllithium: a versatile reagent for the determination of absolute configuration of six-membered ring ketones. Tetrahedron: Asymmetry 1994; 5: 503-506. (Pubitemid 24131763)
    • (1994) Tetrahedron Asymmetry , vol.5 , Issue.4 , pp. 503-506
    • Preite, M.D.1    Gonzalez-Sierra, M.2    Zinczuk, J.3    Ruveda, E.A.4
  • 132
    • 4844221913 scopus 로고
    • Female sex pheromone of the German cockroach, Blattella germanica (L.) (Orthoptera: Blattellidae), responsible for male wing-raising. IV. The absolute configuration of the pheromone, 3,11-dimethyl-2-nonacosanone
    • Nishida R, Kuwahara Y, Fukami H, Ishii S,. Female sex pheromone of the German cockroach, Blattella germanica (L.) (Orthoptera: Blattellidae), responsible for male wing-raising. IV. The absolute configuration of the pheromone, 3,11-dimethyl-2-nonacosanone. J Chem Ecol 1979; 5: 289-297.
    • (1979) J Chem Ecol , vol.5 , pp. 289-297
    • Nishida, R.1    Kuwahara, Y.2    Fukami, H.3    Ishii, S.4
  • 133
    • 84986505860 scopus 로고
    • NMR determination of absolute configurations in 2-alkylthiazolidine-4- carboxylic acids
    • Restelli A, Annunziata R, Pellacini F, Ferrario F,. NMR determination of absolute configurations in 2-alkylthiazolidine-4-carboxylic acids. J Heterocycl Chem 1990; 27: 1035-1039.
    • (1990) J Heterocycl Chem , vol.27 , pp. 1035-1039
    • Restelli, A.1    Annunziata, R.2    Pellacini, F.3    Ferrario, F.4
  • 134
    • 33845375849 scopus 로고
    • Chiral 3-substituted aldehydes: Determination of absolute configurations and enantiomeric excesses by NMR analysis of derived oxazolidines
    • Agami C, Meynier F, Belan J, Besace Y, Brochard L,. Chiral 3-substituted aldehydes: determination of absolute configurations and enantiomeric excesses by NMR analysis of derived oxazolidines. J Org Chem 1986; 51: 73-75.
    • (1986) J Org Chem , vol.51 , pp. 73-75
    • Agami, C.1    Meynier, F.2    Belan, J.3    Besace, Y.4    Brochard, L.5
  • 135
    • 0000209750 scopus 로고
    • Resolution and determination of enantiomeric excesses of chiral aldehydes via chiral imidazolidines
    • Mangeney P, Alexakis A, Normant JF,. Resolution and determination of enantiomeric excesses of chiral aldehydes via chiral imidazolidines. Tetrahedron Lett 1988; 29: 2677-2680.
    • (1988) Tetrahedron Lett , vol.29 , pp. 2677-2680
    • Mangeney, P.1    Alexakis, A.2    Normant, J.F.3
  • 136
    • 0002835303 scopus 로고    scopus 로고
    • Configurational correlations for chiral epoxides by nuclear magnetic resonance spectroscopy in optically active solvents
    • Moretti I, Taddei F, Torre G, Spassky N,. Configurational correlations for chiral epoxides by nuclear magnetic resonance spectroscopy in optically active solvents. Chem Commun 1973: 25-26.
    • Chem Commun , vol.1973 , pp. 25-26
    • Moretti, I.1    Taddei, F.2    Torre, G.3    Spassky, N.4
  • 137
    • 0000960849 scopus 로고
    • Use of chiral lanthanide shift reagents in the determination of enantiomer composition and absolute configuration of epoxides and arene oxides
    • Yeh HJC, Balani SK, Yagi H, Greene RME, Sharma ND, Boyd DR, Jerina DM,. Use of chiral lanthanide shift reagents in the determination of enantiomer composition and absolute configuration of epoxides and arene oxides. J Org Chem 1986; 51: 5439-5443.
    • (1986) J Org Chem , vol.51 , pp. 5439-5443
    • Yeh, H.J.C.1    Balani, S.K.2    Yagi, H.3    Greene, R.M.E.4    Sharma, N.D.5    Boyd, D.R.6    Jerina, D.M.7
  • 138
    • 84989625581 scopus 로고
    • Chiral phenyl-substituted chalcone epoxides. I. Correlative determination of absolute configuration by 1H NMR lanthanide-induced shifts
    • Langin-Lantéri M, Fonbonne C, Huet J, Petit-Ramel M,. Chiral phenyl-substituted chalcone epoxides. I. Correlative determination of absolute configuration by 1H NMR lanthanide-induced shifts. Magn Reson Chem 1987; 25: 216-218.
    • (1987) Magn Reson Chem , vol.25 , pp. 216-218
    • Langin-Lantéri, M.1    Fonbonne, C.2    Huet, J.3    Petit-Ramel, M.4
  • 139
    • 0034619611 scopus 로고    scopus 로고
    • Theoretical and experimental aspects of enantiomeric differentiation using natural abundance multinuclear NMR spectroscopy in chiral polypeptide liquid crystals
    • Sarfati M, Lesot P, Merlet D, Courtieu J,. Theoretical and experimental aspects of enantiomeric differentiation using natural abundance multinuclear NMR spectroscopy in chiral polypeptide liquid crystals. Chem Commun 2000: 2069-2081.
    • Chem Commun , vol.2000 , pp. 2069-2081
    • Sarfati, M.1    Lesot, P.2    Merlet, D.3    Courtieu, J.4
  • 140
    • 36148981416 scopus 로고    scopus 로고
    • Empirical determination of the absolute configuration of small chiral molecules using natural abundance 2H NMR in chiral liquid crystals
    • Ziani L, Lesot P, Meddour A, Courtieu J,. Empirical determination of the absolute configuration of small chiral molecules using natural abundance 2H NMR in chiral liquid crystals. Chem Commun 2007: 4737-4739.
    • Chem Commun , vol.2007 , pp. 4737-4739
    • Ziani, L.1    Lesot, P.2    Meddour, A.3    Courtieu, J.4
  • 141
    • 2542510038 scopus 로고    scopus 로고
    • 1H NMR
    • DOI 10.1016/S0957-4166(98)00048-2, PII S0957416698000482
    • García-Martínez C, Taguchi Y, Oishi A, Hayamizu K,. Ring current effects of phenyl and naphthyl groups: internal probes for determining the absolute configuration of chiral azetidin-2-ones by 1H NMR. Tetrahedron: Asymmetry 1998; 9: 955-965. (Pubitemid 28168105)
    • (1998) Tetrahedron Asymmetry , vol.9 , Issue.6 , pp. 955-965
    • Garcia-Martinez, C.1    Taguchi, Y.2    Oishi, A.3    Hayamizu, K.4
  • 142
    • 0000953504 scopus 로고    scopus 로고
    • Choosing the Right Reagent for the Determination of the Absolute Configuration of Amines by NMR: MTPA or MPA?
    • Seco JM, Latypov SK, Quiñoá E, Riguera R,. Choosing the right reagent for the determination of the absolute configuration of amines by NMR: MTPA or MPA? J Org Chem 1997; 62: 7569-7574. (Pubitemid 127494400)
    • (1997) Journal of Organic Chemistry , vol.62 , Issue.22 , pp. 7569-7574
    • Seco, J.M.1    Latypov, Sh.K.2    Quinoa, E.3    Riguera, R.4
  • 143
    • 0025790925 scopus 로고
    • Elucidation of the absolute configurations of amino acids and amines by the modified Mosher's method
    • Kusumi T, Fukushima T, Ohtani I, Kakisawa H,. Elucidation of the absolute configurations of amino acids and amines by the modified Mosher's method. Tetrahedron Lett 1991; 32: 2939-2942.
    • (1991) Tetrahedron Lett , vol.32 , pp. 2939-2942
    • Kusumi, T.1    Fukushima, T.2    Ohtani, I.3    Kakisawa, H.4
  • 145
    • 0344086176 scopus 로고    scopus 로고
    • Boc-phenylglycine: The reagent of choice for the assignment of the absolute configuration of α-chiral primary amines by 1H NMR spectroscopy
    • Seco JM, Quiñoá E, Riguera R,. Boc-phenylglycine: the reagent of choice for the assignment of the absolute configuration of α-chiral primary amines by 1H NMR spectroscopy. J Org Chem 1999; 64: 4669-4675.
    • (1999) J Org Chem , vol.64 , pp. 4669-4675
    • Seco, J.M.1    Quiñoá, E.2    Riguera, R.3
  • 146
    • 0000424872 scopus 로고    scopus 로고
    • Nonreductive enantioselective ring opening of N-(methylsulfonyl) dicarboximides with diisopropoxytitanium α,α,α′, α′-tetraaryl-1,3-dioxolane-4,5- dimethanolate
    • Ramõn DJ, Guillena G, Seebach D,. Nonreductive enantioselective ring opening of N-(methylsulfonyl)dicarboximides with Diisopropoxytitanium α,α,α',α'-tetraaryl-1,3-dioxolane-4,5-dimethanolate. Helv Chim Acta 1996; 79: 875-894. (Pubitemid 126497794)
    • (1996) Helvetica Chimica Acta , vol.79 , Issue.3 , pp. 875-894
    • Ramon, D.J.1    Guillena, G.2    Seebach, D.3
  • 147
    • 0001356627 scopus 로고
    • On the use of O-methylmandelic acid for the establishment of absolute configuration of α-chiral primary amines
    • Trost BM, Bunt RC, Pulley SR,. On the use of O-methylmandelic acid for the establishment of absolute configuration of α-chiral primary amines. J Org Chem 1994; 59: 4202-4205.
    • (1994) J Org Chem , vol.59 , pp. 4202-4205
    • Trost, B.M.1    Bunt, R.C.2    Pulley, S.R.3
  • 148
    • 36849091867 scopus 로고    scopus 로고
    • Determination of the absolute configuration of primary amines in polar NMR solvents
    • Ahn HC, Choi K,. Determination of the absolute configuration of primary amines in polar NMR solvents. Chem Lett 2007; 36: 1330-1331.
    • (2007) Chem Lett , vol.36 , pp. 1330-1331
    • Ahn, H.C.1    Choi, K.2
  • 149
    • 58149150975 scopus 로고    scopus 로고
    • (1-naphthyl)(trifluoromethyl) O-carboxy anhydride as a chiral derivatizing agent: Eclipsed conformation enforced by hydrogen bonding
    • du Boullay OT, Alba A, Oukhatar F, Mantin-Vaca B, Bourissou D,. (1-naphthyl)(trifluoromethyl) O-carboxy anhydride as a chiral derivatizing agent: eclipsed conformation enforced by hydrogen bonding. Org Lett 2008; 10: 4669-4672.
    • (2008) Org Lett , vol.10 , pp. 4669-4672
    • Du Boullay, O.T.1    Alba, A.2    Oukhatar, F.3    Mantin-Vaca, B.4    Bourissou, D.5
  • 150
    • 0000959494 scopus 로고
    • Optically active NMR solvents VI. The determination of optical purity and absolute configuration of amines
    • Pirkle WH, Burlingame TG, Beare SD,. Optically active NMR solvents VI. The determination of optical purity and absolute configuration of amines. Tetrahedron Lett 1968; 9: 5849-5852.
    • (1968) Tetrahedron Lett , vol.9 , pp. 5849-5852
    • Pirkle, W.H.1    Burlingame, T.G.2    Beare, S.D.3
  • 151
    • 0000089084 scopus 로고
    • A determination method of absolute configuration
    • Toda F, Mori K, Sato A,. A determination method of absolute configuration. Bull Chem Soc Jpn 1988; 61: 4167-4169.
    • (1988) Bull Chem Soc Jpn , vol.61 , pp. 4167-4169
    • Toda, F.1    Mori, K.2    Sato, A.3
  • 152
    • 33845279410 scopus 로고
    • α-Methoxy-α-(trifluoromethyl)benzyl isocyanate. A convenient reagent for the determination of the enantiomeric composition of primary and secondary amines
    • Nabeya A, Endo T,. α-Methoxy-α-(trifluoromethyl)benzyl isocyanate. A convenient reagent for the determination of the enantiomeric composition of primary and secondary amines. J Org Chem 1988; 53: 3358-3361.
    • (1988) J Org Chem , vol.53 , pp. 3358-3361
    • Nabeya, A.1    Endo, T.2
  • 153
    • 0000931413 scopus 로고
    • Improved chiral derivatizing agents for the chromatographic resolution of racemic primary amines
    • Pirkle WH, Simmons KA,. Improved chiral derivatizing agents for the chromatographic resolution of racemic primary amines. J Org Chem 1983; 48: 2520-2527.
    • (1983) J Org Chem , vol.48 , pp. 2520-2527
    • Pirkle, W.H.1    Simmons, K.A.2
  • 154
    • 0011894043 scopus 로고
    • A simple method for distinguishing optical isomers of chiral amines, hydroxylamines, amino acids, and peptides
    • Kolasa T, Miller MJ,. A simple method for distinguishing optical isomers of chiral amines, hydroxylamines, amino acids, and peptides. J Org Chem 1986; 51: 3055-3058.
    • (1986) J Org Chem , vol.51 , pp. 3055-3058
    • Kolasa, T.1    Miller, M.J.2
  • 155
    • 33644773399 scopus 로고    scopus 로고
    • Simple protocol for NMR analysis of the enantiomeric purity of primary amines
    • DOI 10.1021/ol052776g
    • Pérez-Fuertes Y, Kelly AM, Johnson AL, Arimori S, Bull SD, James TD,. Simple protocol for NMR analysis of the enantiomeric purity of primary amines. Org Lett 2006; 8: 609-612. (Pubitemid 43341971)
    • (2006) Organic Letters , vol.8 , Issue.4 , pp. 609-612
    • Perez-Fuertes, Y.1    Kelly, A.M.2    Johnson, A.L.3    Arimori, S.4    Bull, S.D.5    James, T.D.6
  • 156
    • 0003124526 scopus 로고
    • New chiral shift reagents, optically active 2,2'-dihydroxy-1,1'- binaphthyl and 1,6-di(o-chlorophenyl)-1,6-diphenylhexa-2,4-diyne-1,6-diol
    • Toda F, Mori K, Okada J, Node M, Itoh A, Oomine K, Fuji K,. New chiral shift reagents, optically active 2,2'-dihydroxy-1,1'-binaphthyl and 1,6-di(o-chlorophenyl)-1,6-diphenylhexa-2,4-diyne-1,6-diol. Chem Lett 1988; 17: 131-134.
    • (1988) Chem Lett , vol.17 , pp. 131-134
    • Toda, F.1    Mori, K.2    Okada, J.3    Node, M.4    Itoh, A.5    Oomine, K.6    Fuji, K.7
  • 157
    • 0001692739 scopus 로고    scopus 로고
    • MTPA (Mosher) amides of cyclic secondary amines: Conformational aspects and a useful method for assignment of amine configuration
    • Hoye TR, Renner MK,. MTPA (Mosher) amides of cyclic secondary amines: conformational aspects and a useful method for assignment of amine configuration. J Org Chem 1996; 61: 2056-2064.
    • (1996) J Org Chem , vol.61 , pp. 2056-2064
    • Hoye, T.R.1    Renner, M.K.2
  • 158
    • 0000709690 scopus 로고    scopus 로고
    • Applications of MTPA (Mosher) amides of secondary amines: Assignment of absolute configuration in chiral cyclic amines
    • Hoye TR, Renner MK,. Applications of MTPA (Mosher) amides of secondary amines: assignment of absolute configuration in chiral cyclic amines. J Org Chem 1996; 61: 8489-8495. (Pubitemid 126528191)
    • (1996) Journal of Organic Chemistry , vol.61 , Issue.24 , pp. 8489-8495
    • Hoye, T.R.1    Renner, M.K.2
  • 159
    • 29544451711 scopus 로고    scopus 로고
    • Assignment of absolute configuration of cyclic secondary amines by NMR techniques using Mosher's method: A general procedure exemplified with (-)-isoanabasine
    • Kang CQ, Guo HQ, Qiu XP, Bai XL, Yao HB, Gao LX,. Assignment of absolute configuration of cyclic secondary amines by NMR techniques using Mosher's method: a general procedure exemplified with (-)-isoanabasine. Magn Reson Chem 2006; 44: 20-24.
    • (2006) Magn Reson Chem , vol.44 , pp. 20-24
    • Kang, C.Q.1    Guo, H.Q.2    Qiu, X.P.3    Bai, X.L.4    Yao, H.B.5    Gao, L.X.6
  • 160
    • 35548981851 scopus 로고    scopus 로고
    • Assignment of absolute configuration on the basis of the conformational effects induced by chiral derivatizing agents: The 2-arylpyrrolidine case
    • Vidal P, Pedregal C, Diaz N, Broughton H, Acena JL, Jimenez A, Espinosa JF,. Assignment of absolute configuration on the basis of the conformational effects induced by chiral derivatizing agents: the 2-arylpyrrolidine case. Org Lett 2007; 9: 4123-4126.
    • (2007) Org Lett , vol.9 , pp. 4123-4126
    • Vidal, P.1    Pedregal, C.2    Diaz, N.3    Broughton, H.4    Acena, J.L.5    Jimenez, A.6    Espinosa, J.F.7
  • 161
    • 38949128377 scopus 로고    scopus 로고
    • The use of MPA amide for the assignment of absolute configuration of a sterically hindered cyclic secondary amine by 'mix and shake' NMR method
    • Gao J, Haas H, Wang KY, Chen Z, Breitenstein W, Rajan S,. The use of MPA amide for the assignment of absolute configuration of a sterically hindered cyclic secondary amine by 'mix and shake' NMR method. Magn Reson Chem 2007; 46: 17-22.
    • (2007) Magn Reson Chem , vol.46 , pp. 17-22
    • Gao, J.1    Haas, H.2    Wang, K.Y.3    Chen, Z.4    Breitenstein, W.5    Rajan, S.6
  • 162
    • 33645791369 scopus 로고    scopus 로고
    • Asymmetric synthesis at nitrogen by oxidation of imines with m-chloroperbenzoic acid in the presence of optically active carbinols. Absolute stereochemistry of chiral alcohol-imine-peracid solvates
    • Bucciarelli M, Forni A, Moretti I, Torre G,. Asymmetric synthesis at nitrogen by oxidation of imines with m-chloroperbenzoic acid in the presence of optically active carbinols. Absolute stereochemistry of chiral alcohol-imine-peracid solvates. J Chem Soc, Perkin Trans 1 1980: 2152-2161.
    • J Chem Soc, Perkin Trans 1 , vol.1980 , pp. 2152-2161
    • Bucciarelli, M.1    Forni, A.2    Moretti, I.3    Torre, G.4
  • 163
    • 51649125972 scopus 로고    scopus 로고
    • Cross interaction between auxiliaries: The chirality of amino alcohols by NMR
    • Leiro V, Seco JM, Quinoa E, Riguera R,. Cross interaction between auxiliaries: the chirality of amino alcohols by NMR. Org Lett 2008; 10: 2729-2732.
    • (2008) Org Lett , vol.10 , pp. 2729-2732
    • Leiro, V.1    Seco, J.M.2    Quinoa, E.3    Riguera, R.4
  • 164
    • 51649089354 scopus 로고    scopus 로고
    • Assigning the configuration of amino alcohols by NMR; A single derivatization method
    • Leiro V, Seco JM, Quinoa E, Riguera R,. Assigning the configuration of amino alcohols by NMR; a single derivatization method. Org Lett 2008; 10: 2733-2736.
    • (2008) Org Lett , vol.10 , pp. 2733-2736
    • Leiro, V.1    Seco, J.M.2    Quinoa, E.3    Riguera, R.4
  • 165
    • 23944457556 scopus 로고    scopus 로고
    • Enantioselective recognition of 1,2-amino alcohols by reversible formation of imines with resonance-assisted hydrogen bonds
    • DOI 10.1021/ol051267b
    • Kim KM, Park H, Kim H, Chin J, Nam W,. Enantioselective recognition of 1,2-amino alcohols by reversible formation of imines with resonance-assisted hydrogen bonds. Org Lett 2005; 7: 3525-3527. (Pubitemid 41186822)
    • (2005) Organic Letters , vol.7 , Issue.16 , pp. 3525-3527
    • Kwan, M.K.1    Park, H.2    Kim, H.-J.3    Chin, J.4    Nam, W.5
  • 166
    • 2942639912 scopus 로고    scopus 로고
    • Boc-phenylglycine: A chiral solvating agent for the assignment of the absolute configuration of amino alcohols and their ethers by NMR
    • DOI 10.1016/j.tetasy.2004.04.032, PII S0957416604003301
    • Pazos Y, Leiro V, Seco JM, Quiñoá E, Riguera R,. Boc-phenylglycine: a chiral solvating agent for the assignment of the absolute configuration of amino alcohols and their ethers by NMR. Tetrahedron: Asymmetry 2004; 15: 1825-1829. (Pubitemid 38780912)
    • (2004) Tetrahedron Asymmetry , vol.15 , Issue.12 , pp. 1825-1829
    • Pazos, Y.1    Leiro, V.2    Seco, J.M.3    Quinoa, E.4    Riguera, R.5
  • 167
    • 33751391094 scopus 로고
    • A microscale NMR method of determining absolute stereochemistries in β-amino alcohols by enantioselective complexation and the mode of action of their oxidative resolution
    • Potvin PG,. A microscale NMR method of determining absolute stereochemistries in β-amino alcohols by enantioselective complexation and the mode of action of their oxidative resolution. J Org Chem 1992; 57: 3272-3274.
    • (1992) J Org Chem , vol.57 , pp. 3272-3274
    • Potvin, P.G.1
  • 168
    • 0001551621 scopus 로고    scopus 로고
    • 1H NMR of (R)-O-aryllactic acid amides
    • Chinchilla R, Falvello LR, Nájera C,. Determination of the absolute configuration of amines and α-amino acids by 1H NMR of (R)-O-aryllactic acid amides. J Org Chem 1996; 61: 7285-7290. (Pubitemid 126532314)
    • (1996) Journal of Organic Chemistry , vol.61 , Issue.21 , pp. 7285-7290
    • Chinchilla, R.1    Falvello, L.R.2    Najera, C.3
  • 169
    • 0035930797 scopus 로고    scopus 로고
    • Determination of the absolute configurations of α-amino esters from the 19F NMR chemical shifts of their CFTA amide diastereomers
    • Fujiwara T, Omata K, Kabuto K, Kabuto C, Takahashi T, Segawa M, Takeuchi Y,. Determination of the absolute configurations of α-amino esters from the 19F NMR chemical shifts of their CFTA amide diastereomers. Chem Commun 2001: 2694-2695.
    • Chem Commun , vol.2001 , pp. 2694-2695
    • Fujiwara, T.1    Omata, K.2    Kabuto, K.3    Kabuto, C.4    Takahashi, T.5    Segawa, M.6    Takeuchi, Y.7
  • 170
    • 62749156477 scopus 로고    scopus 로고
    • New chiral derivatizing agents: Convenient determination of absolute configurations of free amino acids by 1H NMR
    • Kurosu M, Li K,. New chiral derivatizing agents: convenient determination of absolute configurations of free amino acids by 1H NMR. Org Lett 2009; 11: 911-914.
    • (2009) Org Lett , vol.11 , pp. 911-914
    • Kurosu, M.1    Li, K.2
  • 171
    • 0001123933 scopus 로고
    • Optically active solvents in nuclear magnetic resonance spectroscopy. IX. Direct determinations of optical purities and correlations of absolute configurations of α-amino acids
    • Pirkle WH, Beare SD,. Optically active solvents in nuclear magnetic resonance spectroscopy. IX. Direct determinations of optical purities and correlations of absolute configurations of α-amino acids. J Am Chem Soc 1969; 91: 5150-5155.
    • (1969) J Am Chem Soc , vol.91 , pp. 5150-5155
    • Pirkle, W.H.1    Beare, S.D.2
  • 172
    • 84970582655 scopus 로고
    • Studies on the stereochemical characterization of N-methylated amino acids
    • Ang S, Low SH,. Studies on the stereochemical characterization of N-methylated amino acids. Aust J Chem 1991; 44: 1591-1601.
    • (1991) Aust J Chem , vol.44 , pp. 1591-1601
    • Ang, S.1    Low, S.H.2
  • 173
    • 0037437690 scopus 로고    scopus 로고
    • Nuclear magnetic resonance studies for the chiral recognition of (+)-(R)-18-crown-6-tetracarboxylic acid to amino compounds
    • DOI 10.1016/S0731-7085(02)00537-X, PII S073170850200537X
    • Machida Y, Kagawa M, Nishi H,. Nuclear magnetic resonance studies for the chiral recognition of (+)-(R)-18-crown-6-tetracarboxylic acid to amino compounds. J Pharm Biomed Anal 2003; 30: 1929-1942. (Pubitemid 35453998)
    • (2003) Journal of Pharmaceutical and Biomedical Analysis , vol.30 , Issue.6 , pp. 1929-1942
    • Machida, Y.1    Kagawa, M.2    Nishi, H.3
  • 174
    • 1842319547 scopus 로고
    • Enantiomeric shift difference induced by the lanthanide shift reagent: Its correlation with absolute configuration of α-amino acids
    • Ajisaka K, Kamisaku M, Kainosho M,. Enantiomeric shift difference induced by the lanthanide shift reagent: its correlation with absolute configuration of α-amino acids. Chem Lett 1972; 1: 857-858.
    • (1972) Chem Lett , vol.1 , pp. 857-858
    • Ajisaka, K.1    Kamisaku, M.2    Kainosho, M.3
  • 175
    • 4143107235 scopus 로고    scopus 로고
    • 1H chemical shift non-equivalence of several α-amino ester signals using tris[3- (trifluoromethylhydroxymethylene)-(+)-camphorato]samarium(III): A chiral lanthanide shift reagent that causes minimal line broadening
    • DOI 10.1016/j.tetasy.2004.06.021, PII S0957416604004483
    • Omata K, Aoyagi S, Kabuto K,. Observing the enantiomeric 1H chemical shift non-equivalence of several α-amino ester signals using tris[3-(trifluoromethylhydroxy-methylene)-(+)-camphorato]samarium(III): a chiral lanthanide shift reagent that causes minimal line bordering. Tetrahedron: Asymmetry 2004; 15: 2351-2356. (Pubitemid 39092297)
    • (2004) Tetrahedron Asymmetry , vol.15 , Issue.15 , pp. 2351-2356
    • Omata, K.1    Aoyagi, S.2    Kabuto, K.3
  • 176
    • 37049083982 scopus 로고    scopus 로고
    • Highly consistent correlation between absolute configuration of α-amino acids and their shift induced by the NMR chiral shift reagent propylenediaminetetraacetatoeuropium(III) in aqueous solution
    • Kabuto K, Sasaki Y,. Highly consistent correlation between absolute configuration of α-amino acids and their shift induced by the NMR chiral shift reagent propylenediaminetetraacetatoeuropium(III) in aqueous solution. Chem Commun 1987: 670-671.
    • Chem Commun , vol.1987 , pp. 670-671
    • Kabuto, K.1    Sasaki, Y.2
  • 177
    • 0009531638 scopus 로고    scopus 로고
    • A europium(III)-N,N,N',N'-tetrakis(2-pyridylmethyl)-(R)-propylenediamine complex as a new chiral lanthanide NMR shift reagent for aqueous neutral solution
    • Hazama R, Umakoshi K, Kabuto C, Kabuto K, Sasaki Y,. A europium(III)-N,N,N',N'-tetrakis(2-pyridylmethyl)-(R)-propylenediamine complex as a new chiral lanthanide NMR shift reagent for aqueous neutral solution. Chem Commun 1996: 15-16.
    • Chem Commun , vol.1996 , pp. 15-16
    • Hazama, R.1    Umakoshi, K.2    Kabuto, C.3    Kabuto, K.4    Sasaki, Y.5
  • 178
    • 60849089711 scopus 로고    scopus 로고
    • Properties of chiral Ce(III)-tppn complex as a chiral shift reagent in aqueous solution
    • Sato J, Omata K, Kabuto K, Jin H, Umakoshi K, Sasaki Y,. Properties of chiral Ce(III)-tppn complex as a chiral shift reagent in aqueous solution. Kidorui 1998; 32: 58-59.
    • (1998) Kidorui , vol.32 , pp. 58-59
    • Sato, J.1    Omata, K.2    Kabuto, K.3    Jin, H.4    Umakoshi, K.5    Sasaki, Y.6
  • 179
    • 0032821574 scopus 로고    scopus 로고
    • 1H NMR
    • Sato J, Jin H, Omata K, Kabuto K, Sasaki Y,. Resolution of enantiomer signals by diamagnetic lanthanum(III)-N,N,N',N'-tetrakis(2-pyridinylmethyl)-(R)- propylenediamine complex in 1H NMR. Enantiomer 1999; 4: 147-150. (Pubitemid 29410522)
    • (1999) Enantiomer , vol.4 , Issue.2 , pp. 147-150
    • Sato, J.1    Jin, H.-Y.2    Omata, K.3    Kabuto, K.4    Sasaki, Y.5
  • 180
    • 0025133978 scopus 로고
    • A facile NMR method for assigning absolute confirugation of underivatized α-methyl-α-amino acids using a chiral lanthanoid shift reagent for aqueous solution
    • DOI 10.1016/S0040-4039(00)94422-8
    • Kabuto K, Sasaki Y,. A facile NMR method for assigning absolute configuration of underivatized α-methyl-α-amino acids using a chiral lanthanoid shift reagent for aqueous solution. Tetrahedron Lett 1990; 31: 1031-1034. (Pubitemid 20051563)
    • (1990) Tetrahedron Letters , vol.31 , Issue.7 , pp. 1031-1034
    • Kabuto, K.1    Sasaki, Y.2
  • 181
    • 63049109575 scopus 로고    scopus 로고
    • Use of Sm(III)-{1,2-propanediamine-N,N,N′,N′-tetra(α, α-dideuterioacetate)} complex for NMR determination of absolute configuration of each α-amino acid in peptide hydrolysate mixtures
    • Omata K, Fujioka M, Kabuto K, Sasaki Y,. Use of Sm(III)-{1,2- propanediamine-N,N,N′,N′-tetra(α,α-dideuterioacetate)} complex for NMR determination of absolute configuration of each α-amino acid in peptide hydrolysate mixtures. Chem Commun 2008: 4903-4905.
    • Chem Commun , vol.2008 , pp. 4903-4905
    • Omata, K.1    Fujioka, M.2    Kabuto, K.3    Sasaki, Y.4
  • 182
    • 67651125025 scopus 로고    scopus 로고
    • Use of diketopiperazines for determining absolute configurations of α-substituted series by 1H NMR spectroscopy
    • Sano S, Nakao M, Takeyasu M, Kitaike S, Yoshioka Y, Nagao Y,. Use of diketopiperazines for determining absolute configurations of α-substituted series by 1H NMR spectroscopy. Heterocycles 2009; 79: 781-789.
    • (2009) Heterocycles , vol.79 , pp. 781-789
    • Sano, S.1    Nakao, M.2    Takeyasu, M.3    Kitaike, S.4    Yoshioka, Y.5    Nagao, Y.6
  • 183
    • 4043095002 scopus 로고    scopus 로고
    • Chiral shift reagent for amino acids based on resonance-assisted hydrogen bonding
    • DOI 10.1021/ol049084x
    • Chin J, Kim DC, Kim H, Panosyan FB, Kim KM,. Chiral shift reagent for amino acids based on resonance-assisted hydrogen bonding. Org Lett 2004; 6: 2591-2593. (Pubitemid 39077776)
    • (2004) Organic Letters , vol.6 , Issue.15 , pp. 2591-2593
    • Chin, J.1    Dong, C.K.2    Kim, H.-J.3    Panosyan, F.B.4    Kwan, M.K.5
  • 184
    • 0037463663 scopus 로고    scopus 로고
    • 31P NMR spectroscopy as a powerful tool for the determination of enantiomeric excess and absolute configurations of α-amino acids
    • Bravo J, Cativiela C, Chaves JE, Navarro R, Urriolabeitia EP,. 31P NMR spectroscopy as a powerful tool for the determination of enantiomeric excess and absolute configurations of α-amino acids. Inorg Chem 2003; 42: 1006-1013.
    • (2003) Inorg Chem , vol.42 , pp. 1006-1013
    • Bravo, J.1    Cativiela, C.2    Chaves, J.E.3    Navarro, R.4    Urriolabeitia, E.P.5
  • 185
    • 33745222302 scopus 로고    scopus 로고
    • A new chiral lanthanide NMR probe for the determination of the enantiomeric purity of α-hydroxy acids and the absolute configuration of α-amino acids in water
    • Dickins RS, Badari A,. A new chiral lanthanide NMR probe for the determination of the enantiomeric purity of α-hydroxy acids and the absolute configuration of α-amino acids in water. Dalton Trans 2006; 35: 3088-3096.
    • (2006) Dalton Trans , vol.35 , pp. 3088-3096
    • Dickins, R.S.1    Badari, A.2
  • 186
    • 61849113251 scopus 로고    scopus 로고
    • A new method proposed for the determination of absolute configurations of α-amino acids
    • Gomez ED, Duddeck H,. A new method proposed for the determination of absolute configurations of α-amino acids. Magn Reson Chem 2009; 47: 222-227.
    • (2009) Magn Reson Chem , vol.47 , pp. 222-227
    • Gomez, E.D.1    Duddeck, H.2
  • 187
    • 0027982608 scopus 로고
    • Use of a selone chiral derivatizing agent for the absolute configurational assignment of stereogenic centers
    • DOI 10.1016/0957-4166(94)80066-9
    • Peng J, Odom JD, Dunlap RB, Silks LA,. Use of a selone chiral derivatizing agent for the absolute configurational assignment of stereogenic centers. Tetrahedron: Asymmetry 1994; 5: 1627-1630. (Pubitemid 24278679)
    • (1994) Tetrahedron Asymmetry , vol.5 , Issue.9 , pp. 1627-1630
    • Peng, J.1    Odom, J.2    Dunlap, R.B.3    Silks III, L.A.4
  • 188
    • 39749161513 scopus 로고    scopus 로고
    • Discrimination of enantiomers of α-amino acids by chiral derivatizing reagents from trans-1,2-diaminocyclohexane
    • DOI 10.1002/chir.20435
    • Kaik M, Gajewy J, Grajewski J, Gawronski J,. Discrimination of enantiomers of α-amino acids by chiral derivatizing reagents from trans-1,2-diaminocyclohexane. Chirality 2008; 20: 301-306. (Pubitemid 351303968)
    • (2008) Chirality , vol.20 , Issue.3-4 , pp. 301-306
    • Kaik, M.1    Gajewy, J.2    Grajewski, J.3    Gawronski, J.4
  • 189
    • 44449157182 scopus 로고    scopus 로고
    • Chiral amino alcohols derived from natural amino acids as chiral solvating agents for carboxylic acids
    • DOI 10.1016/j.tetasy.2008.04.030, PII S0957416608002875
    • Wang W, Shen X, Ma F, Li Z, Zhang C,. Chiral amino alcohols derived from natural amino acids as chiral solvating agents for carboxylic acids. Tetrahedron: Asymmetry 2008; 19: 1193-1199. (Pubitemid 351758812)
    • (2008) Tetrahedron Asymmetry , vol.19 , Issue.10 , pp. 1193-1199
    • Wang, W.1    Shen, X.2    Ma, F.3    Li, Z.4    Zhang, C.5
  • 190
    • 49049098354 scopus 로고    scopus 로고
    • External vs. internal interactions in the enantiodiscrimination of fluorinated α-amino acid derivatives by heptakis[2,3-di-O-acetyl-6-O- (tert-butyldimethylsilyl)]-β-cyclodextrin, a powerful chiral solvating agent for NMR spectroscopy
    • Uccello-Barretta G, Balzano F, Pertici F, Jicsinszky L, Sicoli G, Schurig V,. External vs. internal interactions in the enantiodiscrimination of fluorinated α-amino acid derivatives by heptakis[2,3-di-O-acetyl-6-O- (tert-butyldimethylsilyl)]-β-cyclodextrin, a powerful chiral solvating agent for NMR spectroscopy. Eur J Org Chem 2008: 1855-1863.
    • Eur J Org Chem , vol.2008 , pp. 1855-1863
    • Uccello-Barretta, G.1    Balzano, F.2    Pertici, F.3    Jicsinszky, L.4    Sicoli, G.5    Schurig, V.6
  • 191
    • 70349223813 scopus 로고    scopus 로고
    • (18-Crown-6)-2,3,11,12-tetracarboxylic acid as a chiral NMR solvating agent for determining the enantiomeric purity and absolute configuration of β-amino acids
    • Wenzel TJ, Bourne CE, Clark RL,. (18-Crown-6)-2,3,11,12-tetracarboxylic acid as a chiral NMR solvating agent for determining the enantiomeric purity and absolute configuration of β-amino acids. Tetrahedron: Asymmetry 2009; 20: 2052-2060.
    • (2009) Tetrahedron: Asymmetry , vol.20 , pp. 2052-2060
    • Wenzel, T.J.1    Bourne, C.E.2    Clark, R.L.3
  • 192
    • 34548046718 scopus 로고    scopus 로고
    • Enantiomer signal separation of β-amino acids induced by Eu(III)-pdta; Relation between the absolute configurations and relative shifts of enantiomer signals
    • Sasaki M, Omata K, Kabuto K, Sasaki Y,. Enantiomer signal separation of β-amino acids induced by Eu(III)-pdta; relation between the absolute configurations and relative shifts of enantiomer signals. Kidorui 2003; 42: 198-199.
    • (2003) Kidorui , vol.42 , pp. 198-199
    • Sasaki, M.1    Omata, K.2    Kabuto, K.3    Sasaki, Y.4
  • 193
    • 0034472076 scopus 로고    scopus 로고
    • Determination of enantiomer purity of β- and γ-amino acids by NMR analysis of diastereoisomeric palladium complexes
    • DOI 10.1002/1522-2675(20001220)83:12<3262::AID-HLCA3262>3.0.CO;2-P
    • Böhm A, Seebach D,. Determination of enantiomer purity of β- and γ-amino acids by NMR analysis of diastereoisomeric palladium complexes. Helv Chim Acta 2000; 83: 3262-3278. (Pubitemid 32178912)
    • (2000) Helvetica Chimica Acta , vol.83 , Issue.12 , pp. 3262-3278
    • Bohm, A.1    Seebach, D.2
  • 194
    • 0021247616 scopus 로고
    • A liquid chromatographic method for resolving chiral lactams as their diastereomeric ureide derivatives
    • Pirkle WH, Robertson MR, Hyun MH,. A liquid chromatographic method for resolving chiral lactams as their diastereomeric ureide derivatives. J Org Chem 1984; 49: 2433-2437. (Pubitemid 14096525)
    • (1984) Journal of Organic Chemistry , vol.49 , Issue.13 , pp. 2433-2437
    • Pirkle, W.H.1    Robertson, M.R.2    Hyun, M.H.3
  • 195
    • 9644302464 scopus 로고    scopus 로고
    • Assignment of the absolute configuration of 7-substituted 3-azabicyclo[3.3.1]nonan-2-ones by NMR-titration experiments
    • DOI 10.1016/j.tetasy.2004.10.008, PII S0957416604007657
    • Bauer A, Bach T,. Assignment of the absolute configuration of 7-substituted 3-azabicyclo[3.3.1]nonan-2-ones by NMR-titration experiments. Tetrahedron: Asymmetry 2004; 15: 3799-3803. (Pubitemid 39574801)
    • (2004) Tetrahedron Asymmetry , vol.15 , Issue.23 , pp. 3799-3803
    • Bauer, A.1    Bach, T.2
  • 196
    • 0027248235 scopus 로고
    • Control of the enantiomeric purity and correlation with the absolute configuration of N-protected 2-cyanoglycinates
    • DOI 10.1016/S0957-4166(00)80429-2
    • Hudhomme P, Duguay G,. Control of the enantiomeric purity and correlation with the absolute configuration of N-protected 2-cyanoglycinates. Tetrahedron: Asymmetry 1993; 4: 1891-1900. (Pubitemid 23245810)
    • (1993) Tetrahedron Asymmetry , vol.4 , Issue.8 , pp. 1891-1900
    • Hudhomme, P.1    Duguay, G.2
  • 197
    • 33947298829 scopus 로고
    • Optically active solvents for nuclear magnetic resonance. X. Enantiomeric nonequivalence of sulfinamides, sulfinates, sulfites, thiosulfinates, phosphine oxides, and amine oxides
    • Pirkle WH, Beare SD, Muntz RL,. Optically active solvents for nuclear magnetic resonance. X. Enantiomeric nonequivalence of sulfinamides, sulfinates, sulfites, thiosulfinates, phosphine oxides, and amine oxides. J Am Chem Soc 1969; 91: 4575.
    • (1969) J Am Chem Soc , vol.91 , pp. 4575
    • Pirkle, W.H.1    Beare, S.D.2    Muntz, R.L.3
  • 198
    • 0000449248 scopus 로고
    • Chiral nuclear magnetic resonance solvents. XI. A method for determining the absolute configuration of chiral N,N-dialkylarylamine oxides
    • Pirkle WH, Muntz RL, Paul IC,. Chiral nuclear magnetic resonance solvents. XI. A method for determining the absolute configuration of chiral N,N-dialkylarylamine oxides. J Am Chem Soc 1971; 93: 2817-2819.
    • (1971) J Am Chem Soc , vol.93 , pp. 2817-2819
    • Pirkle, W.H.1    Muntz, R.L.2    Paul, I.C.3
  • 199
    • 0011251273 scopus 로고
    • Absolute configuration at chiral nitrogen in oxaziridines configurational correlations by NMR spectroscopy in optically active solvating agents
    • Forni A, Moretti I, Torre G,. Absolute configuration at chiral nitrogen in oxaziridines configurational correlations by NMR spectroscopy in optically active solvating agents. Tetrahedron Lett 1978; 19: 2941-2944.
    • (1978) Tetrahedron Lett , vol.19 , pp. 2941-2944
    • Forni, A.1    Moretti, I.2    Torre, G.3
  • 202
    • 0002709209 scopus 로고    scopus 로고
    • Assignment of absolute configuration of sulfoxides by NMR. A solvation model
    • Pirkle WH, Beare SD, Muntz RL,. Assignment of absolute configuration of sulfoxides by NMR. A solvation model. Tetrahedron Lett 1974: 2295-2298.
    • Tetrahedron Lett , vol.1974 , pp. 2295-2298
    • Pirkle, W.H.1    Beare, S.D.2    Muntz, R.L.3
  • 203
    • 0030728759 scopus 로고    scopus 로고
    • Enantiomeric excess determination of some chiral sulfoxides by NMR: Use of (S)-Ibuprofenρ and (S)-Naproxenρ as shift reagents
    • PII S0040403997101538
    • Fauconnot L, Nugier-Chauvin C, Noiret N, Patin H,. Enantiomeric excess determination of some chiral sulfoxides by NMR: use of (S)-Ibuprofen and (S)-Naproxen as shift reagents. Tetrahedron Lett 1997; 38: 7875-7878. (Pubitemid 27501890)
    • (1997) Tetrahedron Letters , vol.38 , Issue.45 , pp. 7875-7878
    • Fauconnot, L.1    Nugier-Chauvin, C.2    Noiret, N.3    Patin, H.4
  • 204
    • 0009322477 scopus 로고
    • 1H NMR spectral nonequivalence of sulphoxide enantiomers in the presence of 2,2'-dihydroxy-1,1'-binaphthyl
    • Drabowicz J, Duddeck H,. 1H NMR spectral nonequivalence of sulphoxide enantiomers in the presence of 2,2'-dihydroxy-1,1'-binaphthyl. Sulfur Lett 1989; 10: 37-40.
    • (1989) Sulfur Lett , vol.10 , pp. 37-40
    • Drabowicz, J.1    Duddeck, H.2
  • 205
    • 0000602525 scopus 로고
    • Optically active 4,4',6,6'-tetrachloro-2,2'-bis(hydroxydiphenylmethyl)- biphenyl as a host for optical resolution and a chiral shift reagent
    • Toda F, Toyotaka R, Fukuda H,. Optically active 4,4',6,6'-tetrachloro-2, 2'-bis(hydroxydiphenylmethyl)-biphenyl as a host for optical resolution and a chiral shift reagent. Tetrahedron: Asymmetry 1990; 1: 303-306.
    • (1990) Tetrahedron: Asymmetry , vol.1 , pp. 303-306
    • Toda, F.1    Toyotaka, R.2    Fukuda, H.3
  • 206
    • 33746155686 scopus 로고    scopus 로고
    • Recent progress in application of spectroscopic methods for assigning absolute configuration of optically active sulfoxides
    • DOI 10.2174/157019306775474149
    • Donnoli MI, Superchi S, Rosini C,. Recent progress in application of spectroscopic methods for assigning absolute configuration of optically active sulfoxides. Mini-Reviews Org Chem 2006; 3: 77-92. (Pubitemid 44083035)
    • (2006) Mini-Reviews in Organic Chemistry , vol.3 , Issue.1 , pp. 77-92
    • Donnoli, M.I.1    Superchi, S.2    Rosini, C.3
  • 207
    • 0001615971 scopus 로고
    • Chiral nuclear magnetic resonance solvating agents. Resolution, determination of enantiomeric purity, and assignment of absolute configuration of cyclic and acyclic sulfinate esters
    • Pirkle WH, Hoekstra MS,. Chiral nuclear magnetic resonance solvating agents. Resolution, determination of enantiomeric purity, and assignment of absolute configuration of cyclic and acyclic sulfinate esters. J Am Chem Soc 1976; 98: 1832-1839.
    • (1976) J Am Chem Soc , vol.98 , pp. 1832-1839
    • Pirkle, W.H.1    Hoekstra, M.S.2
  • 208
    • 0002107206 scopus 로고
    • Determination of the optical purity and absolute configuration of enantiomeric aralkylamines
    • Hoyer G, Rosenberg D, Rufer C, Seeger A,. Determination of the optical purity and absolute configuration of enantiomeric aralkylamines. Tetrahedron Lett 1972; 13: 985-988.
    • (1972) Tetrahedron Lett , vol.13 , pp. 985-988
    • Hoyer, G.1    Rosenberg, D.2    Rufer, C.3    Seeger, A.4
  • 209
    • 21844437838 scopus 로고    scopus 로고
    • Effective enantiodifferentiation of spirochalcogenuranes by the dirhodium method: Towards the determination of absolute configurations?
    • DOI 10.1002/chir.20103
    • Gáti T, Tõth G, Drabowicz J, Moeller S, Hofer E, Polavarapu P, Duddeck H,. Effective enantiodifferentiation of spirochalcogenuranes by the dirhodium method: towards the determination of absolute configurations? Chirality 2005; 17: S40-S47. (Pubitemid 40962061)
    • (2005) Chirality , vol.17 , Issue.SUPPL.
    • Gati, T.1    Toth, G.2    Drabowicz, J.3    Moeller, S.4    Hofer, E.5    Polavarapu, P.6    Duddeck, H.7
  • 210
    • 36849024432 scopus 로고    scopus 로고
    • Chiral thiols: The assignment of absolute configuration by 1H NMR
    • Porto S, Seco JM, Ortiz O, Quinoa E, Riguera R,. Chiral thiols: the assignment of absolute configuration by 1H NMR. Org Lett 2007; 9: 5015-5018.
    • (2007) Org Lett , vol.9 , pp. 5015-5018
    • Porto, S.1    Seco, J.M.2    Ortiz, O.3    Quinoa, E.4    Riguera, R.5
  • 211
    • 0242349137 scopus 로고    scopus 로고
    • 1H-NMR of diastereomeric thiol esters
    • Matsugi M, Hagimoto Y, Itoh K, Nojima M, Kita Y,. A simple determination method of the absolute configuration of 1-arylethanthiols by an intramolecular CH/π shielding effect in 1H-NMR of diastereomeric thiol esters. Chem Pharm Bull 2003; 51: 460-462. (Pubitemid 41694829)
    • (2003) Chemical and Pharmaceutical Bulletin , vol.51 , Issue.4 , pp. 460-462
    • Matsugi, M.1    Hagimoto, Y.2    Itoh, K.3    Nojima, M.4    Kita, Y.5
  • 212
    • 67649637594 scopus 로고    scopus 로고
    • Assignment of the absolute configuration of hydroxy- and aminophosphonates by NMR spectroscopy
    • Blazewska KM, Gajda T,. Assignment of the absolute configuration of hydroxy- and aminophosphonates by NMR spectroscopy. Tetrahedron: Asymmetry 2009; 20: 1337-1361.
    • (2009) Tetrahedron: Asymmetry , vol.20 , pp. 1337-1361
    • Blazewska, K.M.1    Gajda, T.2
  • 213
    • 0038738249 scopus 로고    scopus 로고
    • The classical Kagan's amides are still practical NMR chiral shift reagents: Determination of enantiomeric purity of P-chirogenic phospholene oxides
    • DOI 10.1016/S0957-4166(03)00207-6
    • Pakulski Z, Demchuk OM, Kwiatosz R, Osinski PW, Swierczynska W, Pietrusiewicz KM,. The classical Kagan's amides are still practical NMR chiral shift reagents: determination of enantiomeric purity of P-chirogenic phospholene oxides. Tetrahedron: Asymmetry 2003; 14: 1459-1462. (Pubitemid 36588843)
    • (2003) Tetrahedron Asymmetry , vol.14 , Issue.11 , pp. 1459-1462
    • Pakulski, Z.1    Demchuk, O.M.2    Kwiatosz, R.3    Osinski, P.W.4    Swierczynska, W.5    Pietrusiewicz, K.M.6
  • 214
    • 57049130385 scopus 로고    scopus 로고
    • A convenient application of the NMR and CD methodologies for the determination of enantiomeric ratio and absolute configuration of chiral atropoisomeric phosphine oxides
    • Demchuk OM, Swierczynska WS, Pietrusiewicz KM, Woznica M, Wojcik D, Frelek J,. A convenient application of the NMR and CD methodologies for the determination of enantiomeric ratio and absolute configuration of chiral atropoisomeric phosphine oxides. Tetrahedron: Asymmetry 2008; 19: 2339-2345.
    • (2008) Tetrahedron: Asymmetry , vol.19 , pp. 2339-2345
    • Demchuk, O.M.1    Swierczynska, W.S.2    Pietrusiewicz, K.M.3    Woznica, M.4    Wojcik, D.5    Frelek, J.6
  • 215
    • 33744932198 scopus 로고    scopus 로고
    • 1H NMR chemical shifts to determine the absolute configuration and enantiomeric purity for enantiomers of 3,3′- disubstituted-MeO-BIPHEP derivatives
    • DOI 10.1139/V05-230
    • Gorobets E, Parvez M, Wheatley BMM, Keay BA,. Use of 1H NMR chemical shifts to determine the absolute configuration and enantiomeric purity for enantiomers of 3,3′-disubstituted-MeO-BIPHEP derivatives. Can J Chem 2006; 84: 93-98. (Pubitemid 43844802)
    • (2006) Canadian Journal of Chemistry , vol.84 , Issue.2 , pp. 93-98
    • Gorobets, E.1    Parvez, M.2    Wheatley, B.M.M.3    Keay, B.A.4
  • 216
    • 33744952039 scopus 로고    scopus 로고
    • The dirhodium-method in the determination of absolute configurations of phospholene chalcogenides
    • DOI 10.1002/chir.20256
    • Moeller S, Drzazga Z, Pakulski Z, Pietrusiewicz KM, Duddeck H,. The dirhodium-method in the determination of absolute configurations of phospholene chalcogenides. Chirality 2006; 18: 395-397. (Pubitemid 43855622)
    • (2006) Chirality , vol.18 , Issue.6 , pp. 395-397
    • Moeller, S.1    Drzazga, Z.2    Pakulski, Z.3    Pietrusiewicz, K.M.4    Duddeck, H.5
  • 217
    • 0035859706 scopus 로고    scopus 로고
    • Enantiomeric resolution and determination of the absolute configuration of dibenzophosphole 5-oxides
    • DOI 10.1016/S0957-4166(01)00339-1, PII S0957416601003391
    • Durán E, Gordo E, Granell J, Font-Bardía M, Solans X, Velasco D, Lõpez-Calahorra F,. Enantiomeric resolution and determination of the absolute configuration of dibenzophosphole 5-oxides. Tetrahedron: Asymmetry 2001; 12: 1987-1997. (Pubitemid 32924982)
    • (2001) Tetrahedron Asymmetry , vol.12 , Issue.14 , pp. 1987-1997
    • Duran, E.1    Gordo, E.2    Granell, J.3    Font-Bardia, M.4    Solans, X.5    Velasco, D.6    Lopez-Calahorra, F.7
  • 218
    • 0042285392 scopus 로고    scopus 로고
    • [1] evaluation of homochiral t-butyl(phenyl)phosphinothioic acid for the determination of enantiomeric excesses and absolute configurations of α-substituted phosphonates
    • Drescher M, Felsinger S, Hammerschmidt F, Kählig H, Schmidt S, Wuggenig F,. Enzymes in organic chemistry 7. Evaluation of homochiral t-butyl(phenyl)phosphinothioic acid for the determination of enantiomeric excesses and absolute configurations of α-substituted phosphonates. Phosphorus, Sulfur Silicon Relat Elem 1998; 140: 79-93. (Pubitemid 128396123)
    • (1998) Phosphorus, Sulfur and Silicon and Related Elements , vol.140 , pp. 79-93
    • Drescher, M.1    Felsinger, S.2    Hammerschmidt, F.3    Kahlig, H.4    Schmidt, S.5    Wuggenig, F.6
  • 219
    • 37049099046 scopus 로고    scopus 로고
    • The proton magnetic resonance spectra of chiral phosphinate esters. Chemical shift non-equivalence of enantiomers induced by optically active phosphinothioic acids
    • Harger MJP,. The proton magnetic resonance spectra of chiral phosphinate esters. Chemical shift non-equivalence of enantiomers induced by optically active phosphinothioic acids. J Chem Soc, Perkin Trans 2 1980: 1505-1511.
    • J Chem Soc, Perkin Trans 2 , vol.1980 , pp. 1505-1511
    • Harger, M.J.P.1
  • 220
    • 37049093030 scopus 로고    scopus 로고
    • Proton magnetic resonance non-equivalence of the enantiomers of alkylphenylphosphinic amides
    • Harger MJP,. Proton magnetic resonance non-equivalence of the enantiomers of alkylphenylphosphinic amides. J Chem Soc, Perkin Trans 2 1977: 1882-1887.
    • J Chem Soc, Perkin Trans 2 , vol.1977 , pp. 1882-1887
    • Harger, M.J.P.1
  • 221
    • 13044253744 scopus 로고
    • Proton magnetic resonance spectra of menthyl phosphinates
    • Lewis RA, Korpiun O, Mislow K,. Proton magnetic resonance spectra of menthyl phosphinates. J Am Chem Soc 1968; 90: 4847-4853.
    • (1968) J Am Chem Soc , vol.90 , pp. 4847-4853
    • Lewis, R.A.1    Korpiun, O.2    Mislow, K.3
  • 222
    • 0001765212 scopus 로고
    • 1H, 31P, and 13C nuclear magnetic resonance nonequivalence of diastereomeric salts of chiral phosphorus thio acids with optically active amines. A method for determining the optical purity and configuration of chiral phosphorus thio acids
    • Mikolajczyk M, Omelanczuk J, Leitloff M, Drabowicz J, Ejchart A, Jurczak J,. 1H, 31P, and 13C nuclear magnetic resonance nonequivalence of diastereomeric salts of chiral phosphorus thio acids with optically active amines. A method for determining the optical purity and configuration of chiral phosphorus thio acids. J Am Chem Soc 1978; 100: 7003-7008.
    • (1978) J Am Chem Soc , vol.100 , pp. 7003-7008
    • Mikolajczyk, M.1    Omelanczuk, J.2    Leitloff, M.3    Drabowicz, J.4    Ejchart, A.5    Jurczak, J.6
  • 223
    • 0009267666 scopus 로고
    • Synthesis of optically active cyclic phosphorothionates and phosphoramidothionates with insecticidal activity by using a chiral phosphorylating agent
    • Hirashima A, Eto M,. Synthesis of optically active cyclic phosphorothionates and phosphoramidothionates with insecticidal activity by using a chiral phosphorylating agent. Agric Biol Chem 1983; 47: 2831-2839.
    • (1983) Agric Biol Chem , vol.47 , pp. 2831-2839
    • Hirashima, A.1    Eto, M.2
  • 224
    • 79251631817 scopus 로고
    • Asymmetric synthesis of (Rp)- and (Sp)-2-ethyl-, (Rp)-2-pentyloxy-, (Sp)-2-pentylthio- and (Sp)-2-pentylamino-4H-1,3,2-benzodioxaphosphorin 2-oxides
    • Wu S, Casida JE,. Asymmetric synthesis of (Rp)- and (Sp)-2-ethyl-, (Rp)-2-pentyloxy-, (Sp)-2-pentylthio- and (Sp)-2-pentylamino-4H-1,3,2- benzodioxaphosphorin 2-oxides. Phosphorus, Sulfur Silicon Relat Elem 1994; 88: 129-137.
    • (1994) Phosphorus, Sulfur Silicon Relat Elem , vol.88 , pp. 129-137
    • Wu, S.1    Casida, J.E.2
  • 225
    • 0008674170 scopus 로고
    • Thiophosphoryl transfer reactions: A general synthesis and configurational analysis of O-substituted [16O,18O]thiophosphates
    • Cullis PM, Iagrossi A, Rous AJ,. Thiophosphoryl transfer reactions: a general synthesis and configurational analysis of O-substituted [16O,18O]thiophosphates. J Am Chem Soc 1986; 108: 7869-7870.
    • (1986) J Am Chem Soc , vol.108 , pp. 7869-7870
    • Cullis, P.M.1    Iagrossi, A.2    Rous, A.J.3
  • 226
    • 0019320839 scopus 로고
    • Analysis of chiral inorganic [16O, 17O, 18O]thiophosphate and the stereochemistry of the 3-phosphoglycerate kinase reaction
    • Webb MR, Trentham DR,. Analysis of chiral inorganic [16O, 17O, 18O]thiophosphate and the stereochemistry of the 3-phosphoglycerate kinase reaction. J Biol Chem 1980; 255: 1775-1779.
    • (1980) J Biol Chem , vol.255 , pp. 1775-1779
    • Webb, M.R.1    Trentham, D.R.2
  • 227
    • 33847085696 scopus 로고
    • Determination of the absolute configuration of [16O, 17O, 18O]phosphate monoesters by using 31P NMR
    • Buchwald SL, Knowles JR,. Determination of the absolute configuration of [16O, 17O, 18O]phosphate monoesters by using 31P NMR. J Am Chem Soc 1980; 102: 6601-6602.
    • (1980) J Am Chem Soc , vol.102 , pp. 6601-6602
    • Buchwald, S.L.1    Knowles, J.R.2
  • 228
    • 37049068124 scopus 로고    scopus 로고
    • Synthesis and stereochemical analysis of chiral inorganic [16O, 17O, 18O]thiophosphate
    • Arnold JRP, Lowe G,. Synthesis and stereochemical analysis of chiral inorganic [16O, 17O, 18O]thiophosphate. Chem Commun 1986: 865-867.
    • Chem Commun , vol.1986 , pp. 865-867
    • Arnold, J.R.P.1    Lowe, G.2
  • 229
    • 0008519584 scopus 로고
    • Oxygen chiral phosphodiesters. 3. Use of 17O NMR spectroscopy to demonstrate configurational differences in the diastereomers of cyclic 2'-deoxyadenosine 3',5'-[17O, 18O]monophosphate
    • Coderre JA, Mehdi S, Demou PC, Weber R, Traficante DD, Gerlt JA,. Oxygen chiral phosphodiesters. 3. Use of 17O NMR spectroscopy to demonstrate configurational differences in the diastereomers of cyclic 2'-deoxyadenosine 3',5'-[17O, 18O]monophosphate. J Am Chem Soc 1981; 103: 1870-1872.
    • (1981) J Am Chem Soc , vol.103 , pp. 1870-1872
    • Coderre, J.A.1    Mehdi, S.2    Demou, P.C.3    Weber, R.4    Traficante, D.D.5    Gerlt, J.A.6
  • 230
    • 6044235286 scopus 로고
    • Stereo- and regiochemistries of the oxidations of 2-methoxy-5-tert-butyl- 1,3,2-dioxaphosphorinanes and the cyclic methyl 3',5'-phosphite of thymidine by H2O/I2 and O2/AIBN to P-chiral phosphates. 17O NMR assignment of phosphorus configuration to the diastereomeric thymidine cyclic methyl 3',5'-monophosphates
    • Bentrude WG, Sopchik AE, Gajda T,. Stereo- and regiochemistries of the oxidations of 2-methoxy-5-tert-butyl-1,3,2-dioxaphosphorinanes and the cyclic methyl 3',5'-phosphite of thymidine by H2O/I2 and O2/AIBN to P-chiral phosphates. 17O NMR assignment of phosphorus configuration to the diastereomeric thymidine cyclic methyl 3',5'-monophosphates. J Am Chem Soc 1989; 111: 3981-3987.
    • (1989) J Am Chem Soc , vol.111 , pp. 3981-3987
    • Bentrude, W.G.1    Sopchik, A.E.2    Gajda, T.3
  • 231
    • 33847086542 scopus 로고
    • Oxygen chiral phosphodiesters. 2. Enzymatic synthesis and configurational analysis of [α-18O]-2'-deoxyadenosine 5'-diphosphate
    • Coderre JA, Gerlt JA,. Oxygen chiral phosphodiesters. 2. Enzymatic synthesis and configurational analysis of [α-18O]-2'-deoxyadenosine 5'-diphosphate. J Am Chem Soc 1980; 102: 6594-6597.
    • (1980) J Am Chem Soc , vol.102 , pp. 6594-6597
    • Coderre, J.A.1    Gerlt, J.A.2
  • 234
    • 0033597446 scopus 로고    scopus 로고
    • 4Br-4 and its NMR-deduced absolute configuration
    • DOI 10.1016/S0957-4166(99)00134-2, PII S0957416699001342
    • Dunina VV, Kuz'mina LG, Rubina MY, Grishin YK, Veits YA, Kazakova EI,. A resolution of the monodentate P*-chiral phosphine PBut C6H4Br-4 and its NMR-deduced absolute configuration. Tetrahedron: Asymmetry 1999; 10: 1483-1497. (Pubitemid 29272340)
    • (1999) Tetrahedron Asymmetry , vol.10 , Issue.8 , pp. 1483-1497
    • Dunina, V.V.1    Kuz'mina, L.G.2    Rubina, M.Y.3    Grishin, Y.K.4    Veits, Y.A.5    Kazakova, E.I.6
  • 235
    • 33845552807 scopus 로고
    • Resolutions involving metal complexation. Preparation and resolution of (R,S)-methylphenyl(8-quinolyl)phosphine and its arsenic analogue. Crystal and molecular structure of (+)589-[(R)-dimethyl(1-ethyl-α-naphthyl)aminato-C2, N]-[(S)-methylphenyl(8-quinolyl)phosphine]palladium(II) hexafluorophosphate
    • Allen DG, McLaughlin GM, Robertson GB, Steffen WL, Salem G, Wild SB,. Resolutions involving metal complexation. Preparation and resolution of (R,S)-methylphenyl(8-quinolyl)phosphine and its arsenic analogue. Crystal and molecular structure of (+)589-[(R)-dimethyl(1-ethyl-α-naphthyl)aminato-C2, N]-[(S)-methylphenyl(8-quinolyl)phosphine]palladium(II) hexafluorophosphate. Inorg Chem 1982; 21: 1007-1014.
    • (1982) Inorg Chem , vol.21 , pp. 1007-1014
    • Allen, D.G.1    McLaughlin, G.M.2    Robertson, G.B.3    Steffen, W.L.4    Salem, G.5    Wild, S.B.6
  • 236
    • 0001221746 scopus 로고
    • Resolutions involving metal complexation. Resolution of (±)-1-amino-2-(methylphenylarsino)ethane and its phosphorus analogue. Stereochemistry and stability of square-planar bis(bidentate) complexes of bivalent palladium and platinum
    • Martin JWL, Palmer JAL, Wild SB,. Resolutions involving metal complexation. Resolution of (±)-1-amino-2-(methylphenylarsino)ethane and its phosphorus analogue. Stereochemistry and stability of square-planar bis(bidentate) complexes of bivalent palladium and platinum. Inorg Chem 1984; 23: 2664-2668.
    • (1984) Inorg Chem , vol.23 , pp. 2664-2668
    • Martin, J.W.L.1    Palmer, J.A.L.2    Wild, S.B.3
  • 237
    • 0030058555 scopus 로고    scopus 로고
    • Synthesis, determination of enantiomeric purity and structural characterisation of enantiopure (2R,5R)-(+)-2,5-bis-(diphenylphosphino)-hexane, a chiral DPPB analogue
    • DOI 10.1016/0957-4166(96)00016-X
    • Wiesauer C, Kratky C, Weissensteiner W,. Synthesis, determination of enantiomeric purity and structural characterisation of enantiopure (2R,5R)-(+)-2,5-bis-(diphenylphosphino)-hexane, a chiral DPPB analogue. Tetrahedron: Asymmetry 1996; 7: 397-398. (Pubitemid 26064698)
    • (1996) Tetrahedron Asymmetry , vol.7 , Issue.2 , pp. 397-398
    • Wiesauer, C.1    Kratky, C.2    Weissensteiner, W.3
  • 238
    • 0001154102 scopus 로고
    • Determination of the absolute configurations of the epimers of the P-chiral phosphine Ph2PCH2CH2P*Ph(L-(-)-menthyl) by use of two-dimensional NMR spectroscopy in combination with a palladium(II) "reporter complex"
    • Jiang Q, Rüegger H, Venanzi LM,. Determination of the absolute configurations of the epimers of the P-chiral phosphine Ph2PCH2CH2P*Ph(L- (-)-menthyl) by use of two-dimensional NMR spectroscopy in combination with a palladium(II) "reporter complex". J Organomet Chem 1995; 488: 233-240.
    • (1995) J Organomet Chem , vol.488 , pp. 233-240
    • Jiang, Q.1    Rüegger, H.2    Venanzi, L.M.3
  • 239
    • 84945431533 scopus 로고
    • 35. Axially dissymmetric diphosphines in the biphenyl series: Synthesis of (6,6'-dimethoxybiphenyl-2,2'-diyl)bis(diphenylphosphine) ('MeO-BIPHEP') and analogues via an ortho-lithiation/iodination Ullmann-reaction approach
    • Schmid R, Foricher J, Cereghetti M, Schönholzer P,. 35. Axially dissymmetric diphosphines in the biphenyl series: synthesis of (6,6'-dimethoxybiphenyl-2,2'-diyl)bis(diphenylphosphine) ('MeO-BIPHEP') and analogues via an ortho-lithiation/iodination Ullmann-reaction approach. Helv Chim Acta 1991; 74: 370-389.
    • (1991) Helv Chim Acta , vol.74 , pp. 370-389
    • Schmid, R.1    Foricher, J.2    Cereghetti, M.3    Schönholzer, P.4
  • 240
    • 33748478792 scopus 로고    scopus 로고
    • An NMR study of the solution conformations of di(tertiary phosphine) complexes of orthopalladated 1-phenyl-1-(N,N-dimethylamino)ethane
    • McFarlane W, Swarbrick JD, Bookham JL,. An NMR study of the solution conformations of di(tertiary phosphine) complexes of orthopalladated 1-phenyl-1-(N,N-dimethylamino)ethane. J Chem Soc, Dalton Trans 1998; 27: 3233-3238. (Pubitemid 128757148)
    • (1998) Journal of the Chemical Society - Dalton Transactions , Issue.19 , pp. 3233-3238
    • McFarlane, W.1    Swarbrick A, J.D.2    Bookham, J.L.3
  • 242
    • 0033534633 scopus 로고    scopus 로고
    • NMR determination of the absolute configuration of cyclic chiral alkenes
    • DOI 10.1016/S0040-4039(98)02342-9, PII S0040403998023429
    • Fukui H, Fukushi Y, Tahara S,. NMR determination of the absolute configuration of cyclic chiral alkenes. Tetrahedron Lett 1999; 40: 325-328. (Pubitemid 29010614)
    • (1999) Tetrahedron Letters , vol.40 , Issue.2 , pp. 325-328
    • Fukui, H.1    Fukushi, Y.2    Tahara, S.3
  • 243
    • 0001605012 scopus 로고
    • Permethylated β-cyclodextrin as chiral solvating agent for the NMR assignment of the absolute configuration of chiral trisubstituted allenes
    • Uccello-Barretta G, Balzano F, Caporusso AM, Iodice A, Salvadori P,. Permethylated β-cyclodextrin as chiral solvating agent for the NMR assignment of the absolute configuration of chiral trisubstituted allenes. J Org Chem 1995; 60: 2227-2231.
    • (1995) J Org Chem , vol.60 , pp. 2227-2231
    • Uccello-Barretta, G.1    Balzano, F.2    Caporusso, A.M.3    Iodice, A.4    Salvadori, P.5
  • 244
    • 0035847282 scopus 로고    scopus 로고
    • 195Pt NMR spectroscopy and NMR stereochemical investigation
    • DOI 10.1021/jo001165t
    • Uccello-Barretta G, Bernardini R, Balzano F, Salvadori P,. [PtCl3(C2H4)] -[AmH]+ complexes containing chiral secondary amines: use as chiral derivatizing agents for the enantiodiscrimination of unsaturated compounds by 195Pt NMR spectroscopy and NMR stereochemical investigation. J Org Chem 2001; 66: 123-129. (Pubitemid 32057848)
    • (2001) Journal of Organic Chemistry , vol.66 , Issue.1 , pp. 123-129
    • Uccello-Barretta, G.1    Bernardini, R.2    Balzano, F.3    Salvadori, P.4
  • 245
    • 0010596841 scopus 로고
    • Estimation of allene optical purities by nuclear magnetic resonance
    • Pirkle WH, Boeder CW,. Estimation of allene optical purities by nuclear magnetic resonance. J Org Chem 1977; 42: 3697-3700.
    • (1977) J Org Chem , vol.42 , pp. 3697-3700
    • Pirkle, W.H.1    Boeder, C.W.2
  • 246
    • 2342477935 scopus 로고    scopus 로고
    • 1,3-Dipolar addition of nitrones to symmetrically substituted allenes: For the determination of absolute configuration of chiral allenes by NMR spectroscopy
    • DOI 10.1016/j.tetlet.2004.03.161, PII S0040403904007105
    • Kawai T, Kodama K, Ooi T, Kusumi T,. 1,3-Dipolar addition of nitrones to symmetrically substituted allenes: for the determination of absolute configuration of chiral allenes by NMR spectroscopy. Tetrahedron Lett 2004; 45: 4097-4099. (Pubitemid 38581821)
    • (2004) Tetrahedron Letters , vol.45 , Issue.21 , pp. 4097-4099
    • Kawai, T.1    Kodama, K.-H.2    Ooi, T.3    Kusumi, T.4
  • 247
    • 34548019262 scopus 로고    scopus 로고
    • Supramolecular method for the determination of absolute configuration of chiral compounds: Theoretical derivatization and a demonstration for a phenolic crown ether-2-amino-1-ethanol system
    • DOI 10.1021/ac070217c
    • Hirose K, Goshima Y, Wakebe T, Tobe Y, Naemura K,. Supramolecular method for the determination of absolute configuration of chiral compounds: theoretical derivatization and a demonstration for a phenolic crown ether-l 2-amino-1-ethanol system. Anal Chem 2007; 79: 6295-6302. (Pubitemid 47282343)
    • (2007) Analytical Chemistry , vol.79 , Issue.16 , pp. 6295-6302
    • Hirose, K.1    Goshima, Y.2    Wakebe, T.3    Tobe, Y.4    Naemura, K.5
  • 248
    • 6344229751 scopus 로고    scopus 로고
    • Simultaneous assignment of all diastereotopic protons in strychnine using RDCs: PELG as alignment medium for organic molecules
    • DOI 10.1021/jo049867w
    • Thiele CM,. Simultaneous assignment of all diastereotopic protons in strychnine using RDCs: PELG as alignment medium for organic molecules. J Org Chem 2004; 69: 7403-7413. (Pubitemid 39403324)
    • (2004) Journal of Organic Chemistry , vol.69 , Issue.22 , pp. 7403-7413
    • Thiele, C.M.1
  • 249
    • 8844230985 scopus 로고    scopus 로고
    • Stretched poly(dimethylsiloxane) gels as NMR alignment media for apolar and weakly polar organic solvents: An ideal tool for measuring RDCs at low molecular concentrations
    • DOI 10.1021/ja046155e
    • Freudenberger JC, Spiteller P, Bauer R, Kessler H, Luy B,. Stretched poly(dimethylsiloxane) gels as NMR alignment media for apolar and weakly polar organic solvents: an ideal tool for measuring RDCs at low molecular concentrations. J Am Chem Soc 2004; 126: 14690-14691. (Pubitemid 39532130)
    • (2004) Journal of the American Chemical Society , vol.126 , Issue.45 , pp. 14690-14691
    • Freudenberger, J.C.1    Spiteller, P.2    Bauer, R.3    Kessler, H.4    Luy, B.5
  • 250
    • 34748914846 scopus 로고    scopus 로고
    • Stereochemical identification of (R)- and (S)-ibuprofen using residual dipolar couplings, NMR, and modeling
    • DOI 10.1002/chir.20338
    • Marathias VM, Tawa GJ, Goijer I, Back AC,. Stereochemical identification of (R)- and (S)-ibuprofen using residual dipolar couplings, NMR, and modeling. Chirality 2007; 19: 741-750. (Pubitemid 47479822)
    • (2007) Chirality , vol.19 , Issue.9 , pp. 741-750
    • Marathias, V.M.1    Tawa, G.J.2    Goljer, I.3    Bach II, A.C.4
  • 251
    • 75749147990 scopus 로고    scopus 로고
    • Enhancing the orienting properties of poly(γ-benzyl-L-glutamate) by means of additives
    • Marx A, Bottcher B, Thiele CM,. Enhancing the orienting properties of poly(γ-benzyl-L-glutamate) by means of additives. Chem Eur J 2010; 16: 1656-1663.
    • (2010) Chem Eur J , vol.16 , pp. 1656-1663
    • Marx, A.1    Bottcher, B.2    Thiele, C.M.3


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