-
1
-
-
0001585011
-
The determination of optical purity by nuclear magnetic resonance spectroscopy
-
Raban M, Mislow K (1965) The determination of optical purity by nuclear magnetic resonance spectroscopy. Tetrahedron Lett 6: 4249-4253
-
(1965)
Tetrahedron Lett
, vol.6
, pp. 4249-4253
-
-
Raban, M.1
Mislow, K.2
-
2
-
-
0000925469
-
The nonequivalence of physical properties of enantiomers in optically active solvents. Differences in nuclear magnetic resonance spectra. I
-
Pirkle WH (1966) The nonequivalence of physical properties of enantiomers in optically active solvents. Differences in nuclear magnetic resonance spectra. I. J Am Chem Soc 88: 1837
-
(1966)
J Am Chem Soc
, vol.88
, pp. 1837
-
-
Pirkle, W.H.1
-
3
-
-
0001429064
-
Tris[3-(tert-butylhydroxymethylene)-d-camphorato] europium(III). A reagent for determining enantiomeric purity
-
Whitesides GM, Lewis DW (1970) Tris[3-(tert-butylhydroxymethylene)-d- camphorato] europium(III). A reagent for determining enantiomeric purity. J Am Chem Soc 92: 6979-6980
-
(1970)
J Am Chem Soc
, vol.92
, pp. 6979-6980
-
-
Whitesides, G.M.1
Lewis, D.W.2
-
4
-
-
0000451708
-
The nuclear magnetic resonance spectra of enantiomers in optically active liquid crystals
-
Sackmann E, Meiboom S, Snyder LC (1968) The nuclear magnetic resonance spectra of enantiomers in optically active liquid crystals. J Am Chem Soc 90: 2183-2184
-
(1968)
J Am Chem Soc
, vol.90
, pp. 2183-2184
-
-
Sackmann, E.1
Meiboom, S.2
Snyder, L.C.3
-
6
-
-
79956210463
-
Using NMR spectroscopic methods to determine enantiomeric purity and assign absolute stereochemistry
-
Wenzel TJ, Chisholm CD (2011) Using NMR spectroscopic methods to determine enantiomeric purity and assign absolute stereochemistry. Prog NMR Spectrosc 59: 1-63
-
(2011)
Prog NMR Spectrosc
, vol.59
, pp. 1-63
-
-
Wenzel, T.J.1
Chisholm, C.D.2
-
7
-
-
84897004468
-
Spectroscopic analysis: NMR and shift reagents
-
Wenzel TJ (2012) Spectroscopic analysis: NMR and shift reagents. Compr Chirality 8: 545-570
-
(2012)
Compr Chirality
, vol.8
, pp. 545-570
-
-
Wenzel, T.J.1
-
8
-
-
79951503684
-
Assignment of absolute configuration using chiral reagents and NMR spectroscopy
-
Wenzel TJ, Chisholm CD (2011) Assignment of absolute configuration using chiral reagents and NMR spectroscopy. Chirality 23: 190-214
-
(2011)
Chirality
, vol.23
, pp. 190-214
-
-
Wenzel, T.J.1
Chisholm, C.D.2
-
9
-
-
67649637594
-
Assignment of the absolute configuration of hydroxy- and aminophosphonates by NMR spectroscopy
-
Blazewska KM, Gajda T (2009) Assignment of the absolute configuration of hydroxy- and aminophosphonates by NMR spectroscopy. Tetrahedron Asymmetry 20: 1337-1361
-
(2009)
Tetrahedron Asymmetry
, vol.20
, pp. 1337-1361
-
-
Blazewska, K.M.1
Gajda, T.2
-
10
-
-
59849105178
-
Chiral recognition of ethers by NMR spectroscopy
-
Duddeck H, Gomez ED (2009) Chiral recognition of ethers by NMR spectroscopy. Chirality 21: 51-68
-
(2009)
Chirality
, vol.21
, pp. 51-68
-
-
Duddeck, H.1
Gomez, E.D.2
-
11
-
-
33947085552
-
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 (1973) 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 95: 512-519
-
(1973)
J Am Chem Soc
, vol.95
, pp. 512-519
-
-
Dale, J.A.1
Mosher, H.S.2
-
13
-
-
33947303494
-
Nuclear magnetic resonance nonequivalence of diastereomeric esters of α-substituted phenylacetic acids for the determination of stereochemical purity
-
Dale JA, Mosher HS (1968) Nuclear magnetic resonance nonequivalence of diastereomeric esters of α-substituted phenylacetic acids for the determination of stereochemical purity. J Am Chem Soc 90: 3732-3738
-
(1968)
J Am Chem Soc
, vol.90
, pp. 3732-3738
-
-
Dale, J.A.1
Mosher, H.S.2
-
14
-
-
33845376028
-
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 (1986) On the use of the O-methylmandelate ester for establishment of absolute configuration of secondary alcohols. J Org Chem 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
-
15
-
-
0001908387
-
Determination of the absolute configuration of biologically active compounds by the modified Mosher's method
-
Cooper R, Snyder JK (eds) Marcel Dekker, New York
-
Kusumi T, Ohtani I (1999) Determination of the absolute configuration of biologically active compounds by the modified Mosher's method. In: Cooper R, Snyder JK (eds) Biologychemistry interface. Marcel Dekker, New York, pp 103-137
-
(1999)
Biologychemistry Interface
, pp. 103-137
-
-
Kusumi, T.1
Ohtani, I.2
-
16
-
-
77958456241
-
13C NMR as a general tool for the assignment of absolute configuration
-
Louzao I, Seco JM, Quinoa E, Riguera R (2010) 13C NMR as a general tool for the assignment of absolute configuration. Chem Commun 46: 7903-7905
-
(2010)
Chem Commun
, vol.46
, pp. 7903-7905
-
-
Louzao, I.1
Seco, J.M.2
Quinoa, E.3
Riguera, R.4
-
17
-
-
84860160002
-
Selective excitation 1D-NMR experiments for the assignment of the absolute configuration of secondary alcohols
-
Ghiviriga I (2012) Selective excitation 1D-NMR experiments for the assignment of the absolute configuration of secondary alcohols. J Org Chem 77: 3978-3985
-
(2012)
J Org Chem
, vol.77
, pp. 3978-3985
-
-
Ghiviriga, I.1
-
18
-
-
38449102399
-
Mosher ester analysis for the determination of absolute configuration of stereogenic (chiral) carbinol carbons
-
Hoye TR, Jeffrey CS, Shao F (2007) Mosher ester analysis for the determination of absolute configuration of stereogenic (chiral) carbinol carbons. Nat Protoc 2: 2451-2458
-
(2007)
Nat Protoc
, vol.2
, pp. 2451-2458
-
-
Hoye, T.R.1
Jeffrey, C.S.2
Shao, F.3
-
19
-
-
77951174296
-
Long-range shielding effects in the 1H NMR spectra of Mosher-like ester derivatives
-
Hoye TR, Erickson SE, Erickson-Birkedahl SL, Hale CRH, Izgu EC, Mayer MJ, Notz PK, Renner MK (2010) Long-range shielding effects in the 1H NMR spectra of Mosher-like ester derivatives. Org Lett 12: 1768-1771
-
(2010)
Org Lett
, vol.12
, pp. 1768-1771
-
-
Hoye, T.R.1
Erickson, S.E.2
Erickson-Birkedahl, S.L.3
Hale, C.R.H.4
Izgu, E.C.5
Mayer, M.J.6
Notz, P.K.7
Renner, M.K.8
-
20
-
-
67849119665
-
A "shortcut" Mosher ester method to assign configurations of stereocenters in nearly symmetric environments. Fluorous mixture synthesis and structure assignment of petrocortyne A
-
Curran DP, Sui B (2009) A "shortcut" Mosher ester method to assign configurations of stereocenters in nearly symmetric environments. Fluorous mixture synthesis and structure assignment of petrocortyne A. J Am Chem Soc 131: 5411-5413
-
(2009)
J Am Chem Soc
, vol.131
, pp. 5411-5413
-
-
Curran, D.P.1
Sui, B.2
-
21
-
-
0035835949
-
Determination of the absolute stereochemistry of alcohols and amines by NMR of the group directly linked to the chiral derivatizing reagent
-
Latypov SK, Galiullina NF, Aganov AV, Kataev VE, Riguera R (2001) Determination of the absolute stereochemistry of alcohols and amines by NMR of the group directly linked to the chiral derivatizing reagent. Tetrahedron 57: 2231-2236
-
(2001)
Tetrahedron
, vol.57
, pp. 2231-2236
-
-
Latypov, S.K.1
Galiullina, N.F.2
Aganov, A.V.3
Kataev, V.E.4
Riguera, R.5
-
22
-
-
0001659714
-
Chemistry of novel compounds with multifunctional carbon structure. 9. Molecular design, synthetic studies, and NMR investigation of several efficient chiral derivatizing reagents which give very large 19F NMR Δδ values in enantiomeric excess determination
-
Takeuchi Y, Itoh N, Satoh T, Koizumi T, Yamaguchi K (1993) Chemistry of novel compounds with multifunctional carbon structure. 9. Molecular design, synthetic studies, and NMR investigation of several efficient chiral derivatizing reagents which give very large 19F NMR Δδ values in enantiomeric excess determination. J Org Chem 58: 1812-1820
-
(1993)
J Org Chem
, vol.58
, pp. 1812-1820
-
-
Takeuchi, Y.1
Itoh, N.2
Satoh, T.3
Koizumi, T.4
Yamaguchi, K.5
-
23
-
-
67651092279
-
Enzymatic resolution of α-hydroxyphosphinates with two stereogenic centres and determination of absolute configuration of stereoisomers obtained
-
Majewska P, Doskocz M, Lejczak B, Kafarski P (2009) Enzymatic resolution of α-hydroxyphosphinates with two stereogenic centres and determination of absolute configuration of stereoisomers obtained. Tetrahedron Asymmetry 20: 1568-1574
-
(2009)
Tetrahedron Asymmetry
, vol.20
, pp. 1568-1574
-
-
Majewska, P.1
Doskocz, M.2
Lejczak, B.3
Kafarski, P.4
-
24
-
-
0028861537
-
Determination of the absolute configuration of alcohols by low temperature 1H NMR of aryl(methoxy)acetates
-
Seco JM, Latypov S, Quinoa E, Riguera R (1995) Determination of the absolute configuration of alcohols by low temperature 1H NMR of aryl(methoxy)acetates. Tetrahedron Asymmetry 6: 107-110
-
(1995)
Tetrahedron Asymmetry
, vol.6
, pp. 107-110
-
-
Seco, J.M.1
Latypov, S.2
Quinoa, E.3
Riguera, R.4
-
25
-
-
0942277395
-
The assignment of absolute configuration by NMR
-
Seco JM, Quinoa E, Riguera R (2004) The assignment of absolute configuration by NMR. Chem Rev 104: 17-117
-
(2004)
Chem Rev
, vol.104
, pp. 17-117
-
-
Seco, J.M.1
Quinoa, E.2
Riguera, R.3
-
26
-
-
62549153979
-
Lipase-catalyzed resolution of 5-acetoxy-1,2-dihydroxy-1,2,3,4- tetrahydronaphthalene. Application to the synthesis of (+)-(3R,4S)-cis-4- hydroxy-6-deoxyscytalone, a metabolite isolated from Colletotrichum acutatum
-
Jimenez-Teja D, Daoubi M, Collado IG, Hernandez-Galan H (2009) Lipase-catalyzed resolution of 5-acetoxy-1,2-dihydroxy-1,2,3,4- tetrahydronaphthalene. Application to the synthesis of (+)-(3R,4S)-cis-4- hydroxy-6-deoxyscytalone, a metabolite isolated from Colletotrichum acutatum. Tetrahedron 65: 3392-3396
-
(2009)
Tetrahedron
, vol.65
, pp. 3392-3396
-
-
Jimenez-Teja, D.1
Daoubi, M.2
Collado, I.G.3
Hernandez-Galan, H.4
-
27
-
-
43249096726
-
Determination of absolute configurations by X-ray crystallography and 1H NMR anisotropy
-
Harada N (2008) Determination of absolute configurations by X-ray crystallography and 1H NMR anisotropy. Chirality 20: 691-723
-
(2008)
Chirality
, vol.20
, pp. 691-723
-
-
Harada, N.1
-
28
-
-
34249074857
-
Crystalline-state conformational analysis of MαNP esters, powerful resolution and chiral 1H NMR anisotropy tools
-
Kuwahara S, Naito J, Yamamoto Y, Kasai Y, Fujita T, Noro K, Shimanuki K, Akagi M, Watanabe M, Matsumoto T, Watanabe M, Ichikawa A, Harada N (2007) Crystalline-state conformational analysis of MαNP esters, powerful resolution and chiral 1H NMR anisotropy tools. Eur J Org Chem 2007: 1827-1840
-
(2007)
Eur J Org Chem
, vol.2007
, pp. 1827-1840
-
-
Kuwahara, S.1
Naito, J.2
Yamamoto, Y.3
Kasai, Y.4
Fujita, T.5
Noro, K.6
Shimanuki, K.7
Akagi, M.8
Watanabe, M.9
Matsumoto, T.10
Watanabe, M.11
Ichikawa, A.12
Harada, N.13
-
29
-
-
34249002071
-
Conformational analysis of MαNP esters, powerful chiral resolution and 1H NMR anisotropy tools - Aromatic geometry and solvent effects on Δδ values
-
Kasai Y, Sugio A, Sekiguchi S, Kuwahara S, Matsumoto T, Watanabe M, Ichikawa A, Harada N (2007) Conformational analysis of MαNP esters, powerful chiral resolution and 1H NMR anisotropy tools - aromatic geometry and solvent effects on Δδ values. Eur J Org Chem 2007: 1811-1826
-
(2007)
Eur J Org Chem
, vol.2007
, pp. 1811-1826
-
-
Kasai, Y.1
Sugio, A.2
Sekiguchi, S.3
Kuwahara, S.4
Matsumoto, T.5
Watanabe, M.6
Ichikawa, A.7
Harada, N.8
-
30
-
-
60149111405
-
Stereoselective synthesis of 2,3,7- trimethylcyclooctanone and related compounds and determination of their relative and absolute configurations by the MαNP acid method
-
Naito J, Kuwahara S, Watanabe M, Decatur J, Bos PH, Van Summeren RP, Horst BT, Feringa BL, Minnaard AJ, Harada N (2008) Stereoselective synthesis of 2,3,7- trimethylcyclooctanone and related compounds and determination of their relative and absolute configurations by the MαNP acid method. Chirality 20: 1053-1065
-
(2008)
Chirality
, vol.20
, pp. 1053-1065
-
-
Naito, J.1
Kuwahara, S.2
Watanabe, M.3
Decatur, J.4
Bos, P.H.5
Van Summeren, R.P.6
Horst, B.T.7
Feringa, B.L.8
Minnaard, A.J.9
Harada, N.10
-
31
-
-
53749083973
-
Synthesis and enantionpure aliphatic acetylene alcohols and determination of their absolute configurations by 1H NMR and/or X-ray crystallography
-
Sekiguchi S, Akagi M, Naito J, Yamamoto Y, Taji H, Kuwahara S, Watanabe M, Ozawa Y, Toriumi K, Harada N (2008) Synthesis and enantionpure aliphatic acetylene alcohols and determination of their absolute configurations by 1H NMR and/or X-ray crystallography. Eur J Org Chem 2008: 2313-2324
-
(2008)
Eur J Org Chem
, vol.2008
, pp. 2313-2324
-
-
Sekiguchi, S.1
Akagi, M.2
Naito, J.3
Yamamoto, Y.4
Taji, H.5
Kuwahara, S.6
Watanabe, M.7
Ozawa, Y.8
Toriumi, K.9
Harada, N.10
-
32
-
-
79953889240
-
Determination of optical purity and absolute configuration of natural 12-hydroxystearic acid by the 1H NMR anisotropy method
-
Murakami S, Satou K, Kijima T, Watanabe M, Izumi T (2011) Determination of optical purity and absolute configuration of natural 12-hydroxystearic acid by the 1H NMR anisotropy method. Eur J Lipid Sci Technol 113: 450-458
-
(2011)
Eur J Lipid Sci Technol
, vol.113
, pp. 450-458
-
-
Murakami, S.1
Satou, K.2
Kijima, T.3
Watanabe, M.4
Izumi, T.5
-
33
-
-
34249068223
-
(R)-(+)-[VCD(+)945]-4-ethyl-4-methyloctane, the simplest chiral saturated hydrocarbon with a quaternary stereogenic center
-
Fujita T, Obata K, Kuwahara S, Miura N, Nakahashi A, Monde K, Decatur J, Harada N (2007) (R)-(+)-[VCD(+)945]-4-ethyl-4-methyloctane, the simplest chiral saturated hydrocarbon with a quaternary stereogenic center. Tetrahedron Lett 48: 4219-4222
-
(2007)
Tetrahedron Lett
, vol.48
, pp. 4219-4222
-
-
Fujita, T.1
Obata, K.2
Kuwahara, S.3
Miura, N.4
Nakahashi, A.5
Monde, K.6
Decatur, J.7
Harada, N.8
-
34
-
-
77952399715
-
Confirmation by IR of the preferred conformations of CFTA esters in solution: A highly reliable criterion for the stereochemistry assignment of chiral alcohols
-
Omata K, Kotani K, Kabuto K, Fujiwara T, Takeuchi Y (2010) Confirmation by IR of the preferred conformations of CFTA esters in solution: a highly reliable criterion for the stereochemistry assignment of chiral alcohols. Chem Commun 46: 3610-3612
-
(2010)
Chem Commun
, vol.46
, pp. 3610-3612
-
-
Omata, K.1
Kotani, K.2
Kabuto, K.3
Fujiwara, T.4
Takeuchi, Y.5
-
35
-
-
33846922299
-
The assignment of the absolute configuration of diethyl hydroxyl- and aminophosphonates by 1H and 31P NMR using naproxen as a reliable chiral derivatizing agent
-
Blezewska K, Paneth P, Gajda T (2007) The assignment of the absolute configuration of diethyl hydroxyl- and aminophosphonates by 1H and 31P NMR using naproxen as a reliable chiral derivatizing agent. J Org Chem 72: 878-887
-
(2007)
J Org Chem
, vol.72
, pp. 878-887
-
-
Blezewska, K.1
Paneth, P.2
Gajda, T.3
-
36
-
-
79955166372
-
Evaluation of the use of mandelate derivatives to determine the enantiomeric purity and the absolute configuration of secondary cyclohexenols
-
Sarotti AM, Pisano PL, Pellegrinet SC (2011) Evaluation of the use of mandelate derivatives to determine the enantiomeric purity and the absolute configuration of secondary cyclohexenols. Arkivoc 7: 343-357
-
(2011)
Arkivoc
, vol.7
, pp. 343-357
-
-
Sarotti, A.M.1
Pisano, P.L.2
Pellegrinet, S.C.3
-
37
-
-
70349211706
-
An experimental/theoretical approach to determine the optical purity and the absolute configuration of endo- and exo-norborn-5-en- 2-ol using mandelate derivatives
-
Pisano PL, Sarotti AM, Pellegrinet SC (2009) An experimental/theoretical approach to determine the optical purity and the absolute configuration of endo- and exo-norborn-5-en- 2-ol using mandelate derivatives. Tetrahedron Lett 50: 6121-6125
-
(2009)
Tetrahedron Lett
, vol.50
, pp. 6121-6125
-
-
Pisano, P.L.1
Sarotti, A.M.2
Pellegrinet, S.C.3
-
38
-
-
84857212927
-
Diastereoselective preparation of (R)- and (S)-2-methoxy-2-phenylpent-3- ynoic acids and their use as reliable chiral derivatizing agents
-
Perez-Estrada S, Joseph-Nathan P, Jiminez-Vazquez HA, Medina-Lopez ME, Ayala-Mata F, Zepeda LG (2012) Diastereoselective preparation of (R)- and (S)-2-methoxy-2-phenylpent-3- ynoic acids and their use as reliable chiral derivatizing agents. J Org Chem 77: 1640-1652
-
(2012)
J Org Chem
, vol.77
, pp. 1640-1652
-
-
Perez-Estrada, S.1
Joseph-Nathan, P.2
Jiminez-Vazquez, H.A.3
Medina-Lopez, M.E.4
Ayala-Mata, F.5
Zepeda, L.G.6
-
39
-
-
0242286024
-
Application of modified Mosher's method for primary alcohols with a methyl group at C2 position
-
Tsuda M, Toriyabe Y, Endo T, Kobayashi J (2003) Application of modified Mosher's method for primary alcohols with a methyl group at C2 position. Chem Pharm Bull 51: 448-451
-
(2003)
Chem Pharm Bull
, vol.51
, pp. 448-451
-
-
Tsuda, M.1
Toriyabe, Y.2
Endo, T.3
Kobayashi, J.4
-
40
-
-
0000191962
-
Assignment of absolute configuration of 2-substituted-1-propanols by 1H NMR spectroscopy
-
Yasuhara F, Yamaguchi S, Kasai R, Tanaka O (1986) Assignment of absolute configuration of 2-substituted-1-propanols by 1H NMR spectroscopy. Tetrahedron Lett 27: 4033-4034
-
(1986)
Tetrahedron Lett
, vol.27
, pp. 4033-4034
-
-
Yasuhara, F.1
Yamaguchi, S.2
Kasai, R.3
Tanaka, O.4
-
41
-
-
0032550653
-
Assignment of the absolute configuration of β-chiral primary alcohols by NMR: Scope and limitations
-
Latypov SK, Ferreiro MJ, Quinoa E, Riguera R (1998) Assignment of the absolute configuration of β-chiral primary alcohols by NMR: scope and limitations. J Am Chem Soc 120: 4741-4751
-
(1998)
J Am Chem Soc
, vol.120
, pp. 4741-4751
-
-
Latypov, S.K.1
Ferreiro, M.J.2
Quinoa, E.3
Riguera, R.4
-
42
-
-
0001288832
-
Identification of absolute configuration of tertiary alcohols by combination of Mosher's method and conformational analysis
-
Izumi S, Moriyoshi H, Hirata T (1994) Identification of absolute configuration of tertiary alcohols by combination of Mosher's method and conformational analysis. Bull Chem Soc Jpn 67: 2600-2602
-
(1994)
Bull Chem Soc Jpn
, vol.67
, pp. 2600-2602
-
-
Izumi, S.1
Moriyoshi, H.2
Hirata, T.3
-
43
-
-
0033235072
-
Determination of absolute configurations of tertiary alcohols by NMR spectroscopy
-
Takahashi H, Kato N, Iwashima M, Iguchi K (1999) Determination of absolute configurations of tertiary alcohols by NMR spectroscopy. Chem Lett 1181-1182
-
(1999)
Chem Lett
, pp. 1181-1182
-
-
Takahashi, H.1
Kato, N.2
Iwashima, M.3
Iguchi, K.4
-
44
-
-
33947669978
-
Challenging the absence of observable hydrogens in the assignment of absolute configurations by NMR: Application to chiral primary alcohols
-
Freire F, Seco JM, Quinoa E, Riguera R (2007) Challenging the absence of observable hydrogens in the assignment of absolute configurations by NMR: application to chiral primary alcohols. Chem Commun 43: 1456-1458
-
(2007)
Chem Commun
, vol.43
, pp. 1456-1458
-
-
Freire, F.1
Seco, J.M.2
Quinoa, E.3
Riguera, R.4
-
45
-
-
34848883609
-
Myrioneurinol: A novel alkaloid skeleton from Myrioneuton nutans
-
Pham VC, Jossang A, Sevenet T, Nguyen VH, Bodo B (2007) Myrioneurinol: a novel alkaloid skeleton from Myrioneuton nutans. Tetrahedron 63: 11244-11249
-
(2007)
Tetrahedron
, vol.63
, pp. 11244-11249
-
-
Pham, V.C.1
Jossang, A.2
Sevenet, T.3
Nguyen, V.H.4
Bodo, B.5
-
46
-
-
69149096162
-
Application of a modified Mosher's method for the determination of enantiomeric ratio and absolute configuration at C-3 of chiral 1,3-dihydroxy ketones
-
Galman JL, Hailes HC (2009) Application of a modified Mosher's method for the determination of enantiomeric ratio and absolute configuration at C-3 of chiral 1,3-dihydroxy ketones. Tetrahedron Asymmetry 20: 1828-1831
-
(2009)
Tetrahedron Asymmetry
, vol.20
, pp. 1828-1831
-
-
Galman, J.L.1
Hailes, H.C.2
-
47
-
-
38049148690
-
Isolation and absolute configuration determination of aliphatic sulfates as the Daphnia Kairomones inducing morphological defense of a phytoplankton - Part 2
-
Yasumoto K, Nishigami A, Aoi H, Tsuchihashi C, Kasai F, Kusumi T, Ooi T (2008) Isolation and absolute configuration determination of aliphatic sulfates as the Daphnia Kairomones inducing morphological defense of a phytoplankton - Part 2. Chem Pharm Bull 56: 129-132
-
(2008)
Chem Pharm Bull
, vol.56
, pp. 129-132
-
-
Yasumoto, K.1
Nishigami, A.2
Aoi, H.3
Tsuchihashi, C.4
Kasai, F.5
Kusumi, T.6
Ooi, T.7
-
48
-
-
59649128088
-
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 (2009) Absolute configuration of ketone cyanohydrins by 1H NMR: the special case of polar substituted tertiary alcohols. Org Lett 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
-
49
-
-
36849024432
-
Chiral thiols: The assignment of their absolute configuration by 1H NMR
-
Porto S, Seco JM, Ortiz A, Quinoa E, Riguera R (2007) Chiral thiols: the assignment of their absolute configuration by 1H NMR. Org Lett 9: 5015-5018
-
(2007)
Org Lett
, vol.9
, pp. 5015-5018
-
-
Porto, S.1
Seco, J.M.2
Ortiz, A.3
Quinoa, E.4
Riguera, R.5
-
50
-
-
79955104985
-
Determination of the absolute configurations of 4-mercapto-2-alkanones using the 1H NMR anisotropy method and enzyme catalyzed kinetic resolution of the corresponding 4-acetylthio-2-alkanones
-
Wakabayashi M, Wakabayashi H, Eisenreich W, Morimitsu Y, Kubota K, Engel KH (2011) Determination of the absolute configurations of 4-mercapto-2-alkanones using the 1H NMR anisotropy method and enzyme catalyzed kinetic resolution of the corresponding 4-acetylthio-2-alkanones. Eur Food Res Technol 232: 753-760
-
(2011)
Eur Food Res Technol
, vol.232
, pp. 753-760
-
-
Wakabayashi, M.1
Wakabayashi, H.2
Eisenreich, W.3
Morimitsu, Y.4
Kubota, K.5
Engel, K.H.6
-
51
-
-
0344086176
-
Boc-phenylglycine: The reagent of choice for the assignment of the absolute configuration of α-chiral primary amines by 1H NMR spectroscopy
-
Seco JM, Quinoa E, Riguera R (1999) 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 64: 4669-4675
-
(1999)
J Org Chem
, vol.64
, pp. 4669-4675
-
-
Seco, J.M.1
Quinoa, E.2
Riguera, R.3
-
52
-
-
0001376827
-
Determination of the absolute stereochemistry of chiral amines by 1H NMR of arylmethoxyacetic acid amides: The conformational model
-
Latypov SK, Seco JM, Quinoa E, Riguera R (1995) Determination of the absolute stereochemistry of chiral amines by 1H NMR of arylmethoxyacetic acid amides: the conformational model. J Org Chem 60: 1538-1545
-
(1995)
J Org Chem
, vol.60
, pp. 1538-1545
-
-
Latypov, S.K.1
Seco, J.M.2
Quinoa, E.3
Riguera, R.4
-
53
-
-
0001692739
-
MTPA (Mosher) amides of cyclic secondary amines: Conformational aspects and a useful method for assignment of amine configuration
-
Hoye TR, Renner MK (1996) MTPA (Mosher) amides of cyclic secondary amines: conformational aspects and a useful method for assignment of amine configuration. J Org Chem 61: 2056-2064
-
(1996)
J Org Chem
, vol.61
, pp. 2056-2064
-
-
Hoye, T.R.1
Renner, M.K.2
-
54
-
-
0000709690
-
Applications of MTPA (Mosher) amides of secondary amines: Assignment of absolute configuration in chiral cyclic amines
-
Hoye TR, Renner MK (1996) Applications of MTPA (Mosher) amides of secondary amines: assignment of absolute configuration in chiral cyclic amines. J Org Chem 61: 8489-8495
-
(1996)
J Org Chem
, vol.61
, pp. 8489-8495
-
-
Hoye, T.R.1
Renner, M.K.2
-
55
-
-
35548981851
-
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 (2007) Assignment of absolute configuration on the basis of the conformational effects induced by chiral derivatizing agents: the 2-arylpyrrolidine case. Org Lett 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
-
56
-
-
38949128377
-
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 (2008) 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 46: 17-22
-
(2008)
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
-
57
-
-
43049124369
-
Reliable assignment of absolute configuration of chiral amines based on the analysis of 1H NMR spectra of their CFTA amide diastereomers
-
Fujiwara T, Segawa M, Fujisawa H, Murai T, Takahashi T, Omata K, Kabuto K, Lodwig SN, Unkefer CJ, Takeuchi Y (2008) Reliable assignment of absolute configuration of chiral amines based on the analysis of 1H NMR spectra of their CFTA amide diastereomers. Tetrahedron Asymmetry 19: 847-856
-
(2008)
Tetrahedron Asymmetry
, vol.19
, pp. 847-856
-
-
Fujiwara, T.1
Segawa, M.2
Fujisawa, H.3
Murai, T.4
Takahashi, T.5
Omata, K.6
Kabuto, K.7
Lodwig, S.N.8
Unkefer, C.J.9
Takeuchi, Y.10
-
58
-
-
59649130083
-
The absolute configuration of the (+)- and (-)-cis- and (+)- and (-)-trans-1-benzyl-4-hydroxypiperidine-3-methanols: An unusual application of the 1H-NMR Mosher method
-
Clerc C, Matarazzo I, Ruedi P (2009) The absolute configuration of the (+)- and (-)-cis- and (+)- and (-)-trans-1-benzyl-4-hydroxypiperidine-3- methanols: an unusual application of the 1H-NMR Mosher method. Helv Chim Acta 92: 14-28
-
(2009)
Helv Chim Acta
, vol.92
, pp. 14-28
-
-
Clerc, C.1
Matarazzo, I.2
Ruedi, P.3
-
59
-
-
84864688797
-
Assignment of the absolute configuration of polyfunctional compounds by NMR using chiral derivatizing agents
-
Seco JM, Quinoa E, Riguera R (2012) Assignment of the absolute configuration of polyfunctional compounds by NMR using chiral derivatizing agents. Chem Rev 112: 4603-4641
-
(2012)
Chem Rev
, vol.112
, pp. 4603-4641
-
-
Seco, J.M.1
Quinoa, E.2
Riguera, R.3
-
60
-
-
48349138800
-
Resin-bound chiral derivatizing agents for assignment of configuration by NMR spectroscopy
-
Porto S, Seco JM, Espinosa JF, Quinoa E, Riguera R (2008) Resin-bound chiral derivatizing agents for assignment of configuration by NMR spectroscopy. J Org Chem 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
-
61
-
-
0036521430
-
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 (2002) 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 Jpn Acad Ser B Phys Biol Sci 78: 69-72
-
(2002)
Proc Jpn Acad ser B Phys Biol Sci
, vol.78
, pp. 69-72
-
-
Ohrui, H.1
Terashima, H.2
Imaizumi, K.3
Akasaka, K.4
-
62
-
-
0141960406
-
Highly potent chiral labeling reagents for the discrimination of chiral alcohols
-
Imaizumi K, Terasima H, Akasaka K, Ohrui H (2003) Highly potent chiral labeling reagents for the discrimination of chiral alcohols. Anal Sci 19: 1243-1249
-
(2003)
Anal Sci
, vol.19
, pp. 1243-1249
-
-
Imaizumi, K.1
Terasima, H.2
Akasaka, K.3
Ohrui, H.4
-
63
-
-
84996014984
-
Synthesis of a series of fluorescent carboxylic acids with a 1,3-benzodioxole skeleton and their evaluation as chiral derivatizing reagents
-
Nishida Y, Itoh E, Abe M, Ohrui H, Meguro H (1995) Synthesis of a series of fluorescent carboxylic acids with a 1,3-benzodioxole skeleton and their evaluation as chiral derivatizing reagents. Anal Sci 11: 213-220
-
(1995)
Anal Sci
, vol.11
, pp. 213-220
-
-
Nishida, Y.1
Itoh, E.2
Abe, M.3
Ohrui, H.4
Meguro, H.5
-
64
-
-
0013403364
-
Chiral discrimination of branched alkyl chain by labeling with chiral derivatization reagents
-
Akasaka K, Imaizumi K, Sakakibara R, Terashima H, Ohrui H (2000) Chiral discrimination of branched alkyl chain by labeling with chiral derivatization reagents. Tennen Yuki Kagobutsu Toronkai Koen Yoshishu 42: 565-570
-
(2000)
Tennen Yuki Kagobutsu Toronkai Koen Yoshishu
, vol.42
, pp. 565-570
-
-
Akasaka, K.1
Imaizumi, K.2
Sakakibara, R.3
Terashima, H.4
Ohrui, H.5
-
65
-
-
21844475636
-
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
-
Ohtaki T, Akasaka K, Kabuto C,Ohrui H (2005) 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 17:S171-S176
-
(2005)
Chirality
, vol.17
-
-
Ohtaki, T.1
Akasaka, K.2
Kabuto Cohrui, H.3
-
66
-
-
34848813518
-
N-(2-Nitrophenyl)proline: An intramolecular hydrogen bond forming reagent for the determination of the absolute configuration of primary amines
-
Ahn HC, Choi K (2007) N-(2-Nitrophenyl)proline: an intramolecular hydrogen bond forming reagent for the determination of the absolute configuration of primary amines. Org Lett 9: 3853-3855
-
(2007)
Org Lett
, vol.9
, pp. 3853-3855
-
-
Ahn, H.C.1
Choi, K.2
-
67
-
-
36849091867
-
Determination of the absolute configuration of primary amines in polar NMR solvents
-
Ahn HC, Choi K (2007) Determination of the absolute configuration of primary amines in polar NMR solvents. Chem Lett 36: 1330-1331
-
(2007)
Chem Lett
, vol.36
, pp. 1330-1331
-
-
Ahn, H.C.1
Choi, K.2
-
68
-
-
84155163185
-
Asymmetric synthesis and absolute configuration of a planar chiral phosphapalladacycle with a ferrocenyl framework
-
Gorunova ON, Livantsov MV, Grishin YK, Kataeva NA, Kochetkov KA, Churakov AV, Kuz'mina LG, Dunina VV (2012) Asymmetric synthesis and absolute configuration of a planar chiral phosphapalladacycle with a ferrocenyl framework. Polyhedron 31: 37-43
-
(2012)
Polyhedron
, vol.31
, pp. 37-43
-
-
Gorunova, O.N.1
Livantsov, M.V.2
Grishin, Y.K.3
Kataeva, N.A.4
Kochetkov, K.A.5
Churakov, A.V.6
Kuz'Mina, L.G.7
Dunina, V.V.8
-
69
-
-
79956350065
-
N-Arylcarbonylpseudoprolines as tunable chiral derivatizing agents for the determination of the absolute configuration of secondary alcohols
-
Han SY, Choi K (2011) N-Arylcarbonylpseudoprolines as tunable chiral derivatizing agents for the determination of the absolute configuration of secondary alcohols. Eur J Org Chem 2011: 2920-2923
-
(2011)
Eur J Org Chem
, vol.2011
, pp. 2920-2923
-
-
Han, S.Y.1
Choi, K.2
-
70
-
-
67651125025
-
Use of diketopiperazines for determining absolute configurations of α-substituted serines by 1H NMR spectroscopy
-
Sano S, Nakao M, Takeyasu M, Kitaike S, Yoshioka Y, Nagao Y (2009) Use of diketopiperazines for determining absolute configurations of α-substituted serines by 1H NMR spectroscopy. Heterocycles 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
-
71
-
-
76849112766
-
Cyclic ketals of tartaric acid: Simple and tunable reagents for the determination of the absolute configuration of primary amines
-
Shim YJ, Choi K (2010) Cyclic ketals of tartaric acid: simple and tunable reagents for the determination of the absolute configuration of primary amines. Org Lett 12: 880-882
-
(2010)
Org Lett
, vol.12
, pp. 880-882
-
-
Shim, Y.J.1
Choi, K.2
-
72
-
-
78549253787
-
Tetrahydro-1,4-epoxynaphthalene-1-carboxylic acid: A chiral derivatizing agent for the determination of the absolute configuration of secondary alcohols
-
Sungsuwan S, Ruangsupapichart N, Prabpai S, Kongsaeree P, Thongpanchang T (2010) Tetrahydro-1,4-epoxynaphthalene-1-carboxylic acid: a chiral derivatizing agent for the determination of the absolute configuration of secondary alcohols. Tetrahedron Lett 51: 4965-4967
-
(2010)
Tetrahedron Lett
, vol.51
, pp. 4965-4967
-
-
Sungsuwan, S.1
Ruangsupapichart, N.2
Prabpai, S.3
Kongsaeree, P.4
Thongpanchang, T.5
-
73
-
-
58149150975
-
1-Naphthyl) (trifluoromethyl) O-carboxy anhydride as a chiral derivatizing agent: Eclipsed conformation enforced by hydrogen bonding
-
du Boullay OT, Alba A, Oukhatar F, Martin-Vaca B, Bourissou D (2008) (1-Naphthyl) (trifluoromethyl) O-carboxy anhydride as a chiral derivatizing agent: eclipsed conformation enforced by hydrogen bonding. Org Lett 10: 4669-4672
-
(2008)
Org Lett
, vol.10
, pp. 4669-4672
-
-
Du Boullay, O.T.1
Alba, A.2
Oukhatar, F.3
Martin-Vaca, B.4
Bourissou, D.5
-
74
-
-
77954689454
-
Structural analysis of the exopolysaccharide produced by Streptococcus thermophiles ST1 solely by NMR spectroscopy
-
Sawen E, Huttunen E, Zhang X, Yang Z, Widmalm G (2010) Structural analysis of the exopolysaccharide produced by Streptococcus thermophiles ST1 solely by NMR spectroscopy. J Biomol NMR 47: 125-134
-
(2010)
J Biomol NMR
, vol.47
, pp. 125-134
-
-
Sawen, E.1
Huttunen, E.2
Zhang, X.3
Yang, Z.4
Widmalm, G.5
-
75
-
-
0034607851
-
Assignment of the absolute configuration of α-chiral carboxylic acids by 1H NMR spectroscopy
-
Ferreiro MJ, Latypov SK, Quinoa E, Riguera R (2000) Assignment of the absolute configuration of α-chiral carboxylic acids by 1H NMR spectroscopy. J Org Chem 65: 2658-2666
-
(2000)
J Org Chem
, vol.65
, pp. 2658-2666
-
-
Ferreiro, M.J.1
Latypov, S.K.2
Quinoa, E.3
Riguera, R.4
-
76
-
-
62849122560
-
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 (2009) Synthesis of optically active α-benzyl paraconic acids and their esters and assignment of their absolute configuration. Tetrahedron Asymmetry 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
-
77
-
-
81255136691
-
Automatic structure determination of regular polysaccharides based solely on NMR spectroscopy
-
Lundborg M, Fontana C, Widmalm G (2011) Automatic structure determination of regular polysaccharides based solely on NMR spectroscopy. Biomacromolecules 12: 3851-3855
-
(2011)
Biomacromolecules
, vol.12
, pp. 3851-3855
-
-
Lundborg, M.1
Fontana, C.2
Widmalm, G.3
-
78
-
-
79955793184
-
Determination of absolute stereochemistry of natural alicyclic glycosides by 1H NMRspectroscopy without application of chiral reagents - An indication
-
Makarieva TN, Shubina LK, Guzii AG, Ivanchina NV, Denisenko VA, Afiyatullov SS, Dmitrenok PS, Kalinovsky AI, Stonik VA (2011) Determination of absolute stereochemistry of natural alicyclic glycosides by 1H NMRspectroscopy without application of chiral reagents - an indication. Nat Prod Commun 6: 673-676
-
(2011)
Nat Prod Commun
, vol.6
, pp. 673-676
-
-
Makarieva, T.N.1
Shubina, L.K.2
Guzii, A.G.3
Ivanchina, N.V.4
Denisenko, V.A.5
Afiyatullov, S.S.6
Dmitrenok, P.S.7
Kalinovsky, A.I.8
Stonik, V.A.9
-
79
-
-
43149088468
-
Synthesis of 2-aryloxypropanoic acids analogues of clofibric acid and assignment of the absolute configuration by 1H NMR spectroscopy and DFT calculations
-
Ammazzalorso A, Bettoni G, De Filippis B, Fantacuzzi M, Giampietro L, Giancristofaro A, Maccallini C, Re N, Amoroso R, Coletti C (2008) Synthesis of 2-aryloxypropanoic acids analogues of clofibric acid and assignment of the absolute configuration by 1H NMR spectroscopy and DFT calculations. Tetrahedron Asymmetry 19: 989-997
-
(2008)
Tetrahedron Asymmetry
, vol.19
, pp. 989-997
-
-
Ammazzalorso, A.1
Bettoni, G.2
De Filippis, B.3
Fantacuzzi, M.4
Giampietro, L.5
Giancristofaro, A.6
MacCallini, C.7
Re, N.8
Amoroso, R.9
Coletti, C.10
-
80
-
-
0034723380
-
Phenylglycine methyl ester, a useful tool for absolute configuration determination of various chiral carboxylic acids
-
Yabuuchi T, Kusumi T (2000) Phenylglycine methyl ester, a useful tool for absolute configuration determination of various chiral carboxylic acids. J Org Chem 65: 397-404
-
(2000)
J Org Chem
, vol.65
, pp. 397-404
-
-
Yabuuchi, T.1
Kusumi, T.2
-
81
-
-
0028907528
-
New chiral anisotropic reagents for determining the absolute configuration of carboxylic acids
-
Nagai Y, Kusumi T (1995) New chiral anisotropic reagents for determining the absolute configuration of carboxylic acids. Tetrahedron Lett 36: 1853-1856
-
(1995)
Tetrahedron Lett
, vol.36
, pp. 1853-1856
-
-
Nagai, Y.1
Kusumi, T.2
-
82
-
-
0001908387
-
Determination of the absolute configuration of biologically active compounds by the modified Mosher's method
-
Kusumi T, Ohtani II (1999) Determination of the absolute configuration of biologically active compounds by the modified Mosher's method. Biol-Chem Interface 103-137
-
(1999)
Biol-Chem Interface
, pp. 103-137
-
-
Kusumi, T.1
Ohtani, I.I.2
-
83
-
-
0032550683
-
An NMR strategy for determination of configuration of remote stereogenic centers: 3-methylcarboxylic acids
-
Hoye TR, Koltun DO (1998) An NMR strategy for determination of configuration of remote stereogenic centers: 3-methylcarboxylic acids. J Am Chem Soc 120: 4638-4643
-
(1998)
J Am Chem Soc
, vol.120
, pp. 4638-4643
-
-
Hoye, T.R.1
Koltun, D.O.2
-
84
-
-
0034175635
-
An NMR method for determination of configuration of β-substituted carboxylic acids
-
Hoye TR, Hamad AS, Koltun DO, Tennakoon MA (1998) An NMR method for determination of configuration of β-substituted carboxylic acids. Tetrahedron Lett 41: 2289-2293
-
(1998)
Tetrahedron Lett
, vol.41
, pp. 2289-2293
-
-
Hoye, T.R.1
Hamad, A.S.2
Koltun, D.O.3
Tennakoon, M.A.4
-
85
-
-
71849110340
-
Absolute configuration determination of 2-(2-oxo-3-indolyl)acetamide derivatives
-
Suarez-Castillo OR, Melendez-Rodriguez M, Castelan-Duarte LE, Sanchez-Zavala M, Rivera- Becerril E, Morales-Rios MS, Joseph-Nathan P (2009) Absolute configuration determination of 2-(2-oxo-3-indolyl)acetamide derivatives. Tetrahedron Asymmetry 20: 2374-2389
-
(2009)
Tetrahedron Asymmetry
, vol.20
, pp. 2374-2389
-
-
Suarez-Castillo, O.R.1
Melendez-Rodriguez, M.2
Castelan-Duarte, L.E.3
Sanchez-Zavala, M.4
Rivera-Becerril, E.5
Morales-Rios, M.S.6
Joseph-Nathan, P.7
-
86
-
-
39749161513
-
Discrimination of enantiomers of α-amino acids by chiral derivatizing reagents from trans-1,2-diaminocyclohexane
-
Kaik M, Gajewy J, Grajewski J, Gawronski J (2008) Discrimination of enantiomers of α-amino acids by chiral derivatizing reagents from trans-1,2-diaminocyclohexane. Chirality 20: 301-306
-
(2008)
Chirality
, vol.20
, pp. 301-306
-
-
Kaik, M.1
Gajewy, J.2
Grajewski, J.3
Gawronski, J.4
-
87
-
-
68049120089
-
Novel chiral derivatizing isothiocyanate-based agent for the enantiomeric excess determination of amines
-
Sabot C, Mosser M, Antheaume C, Mioskowski C, Baati R, Wagner A (2009) Novel chiral derivatizing isothiocyanate-based agent for the enantiomeric excess determination of amines. Chem Commun 45: 3410-3412
-
(2009)
Chem Commun
, vol.45
, pp. 3410-3412
-
-
Sabot, C.1
Mosser, M.2
Antheaume, C.3
Mioskowski, C.4
Baati, R.5
Wagner, A.6
-
88
-
-
77953565286
-
NMR determinations of the absolute configuration of α-chiral primary amines
-
Fukui H, Fukushi Y (2010) NMR determinations of the absolute configuration of α-chiral primary amines. Org Lett 12: 2856-2859
-
(2010)
Org Lett
, vol.12
, pp. 2856-2859
-
-
Fukui, H.1
Fukushi, Y.2
-
89
-
-
46149115357
-
Effects of ring substituents on enantioselective recognition of amino alcohols and acids in uryl-based binol receptors
-
Nandhakumar R, Ryu J, Park H, Tang L, Choi S, Kim KM (2008) Effects of ring substituents on enantioselective recognition of amino alcohols and acids in uryl-based binol receptors. Tetrahedron 64: 7704-7708
-
(2008)
Tetrahedron
, vol.64
, pp. 7704-7708
-
-
Nandhakumar, R.1
Ryu, J.2
Park, H.3
Tang, L.4
Choi, S.5
Kim, K.M.6
-
90
-
-
57149122415
-
Enantioselective recognition of 1,2-amino alcohols by the binol receptor dangled with pyrrole-2-carboxamide and its analogues
-
Nandhakumar R, Soo AY, Hong J, Ham S, Kim KM (2009) Enantioselective recognition of 1,2-amino alcohols by the binol receptor dangled with pyrrole-2-carboxamide and its analogues. Tetrahedron 65: 666-671
-
(2009)
Tetrahedron
, vol.65
, pp. 666-671
-
-
Nandhakumar, R.1
Soo, A.Y.2
Hong, J.3
Ham, S.4
Kim, K.M.5
-
91
-
-
84856390741
-
Absolute configuration assignment of 3-oxoindolylacetyl-4- phenyloxazolidinone derivatives
-
Suarez-Castillo OR, Melendez-Rodriguez M, Castelan-Duarte LE, Zuniga-Estrada EA, Cruz-Borbolla J, Morales-Rios MS, Joseph-Nathan P (2011) Absolute configuration assignment of 3-oxoindolylacetyl-4-phenyloxazolidinone derivatives. Tetrahedron Asymmetry 22: 2085-2098
-
(2011)
Tetrahedron Asymmetry
, vol.22
, pp. 2085-2098
-
-
Suarez-Castillo, O.R.1
Melendez-Rodriguez, M.2
Castelan-Duarte, L.E.3
Zuniga-Estrada, E.A.4
Cruz-Borbolla, J.5
Morales-Rios, M.S.6
Joseph-Nathan, P.7
-
92
-
-
55249090431
-
Highly stereospecific generation of helical chirality by imprinting with amino acids: A universal sensor for amino acid enantiopurity
-
Kim H, So SM, Yen CPH, Vinhato E, Lough AJ, Hong JI, Kim HJ, Chin J (2008) Highly stereospecific generation of helical chirality by imprinting with amino acids: a universal sensor for amino acid enantiopurity. Angew Chem Int Ed 47: 8657-8660
-
(2008)
Angew Chem Int Ed
, vol.47
, pp. 8657-8660
-
-
Kim, H.1
So, S.M.2
Yen, C.P.H.3
Vinhato, E.4
Lough, A.J.5
Hong, J.I.6
Kim, H.J.7
Chin, J.8
-
93
-
-
75149189928
-
Chiral discrimination of α-amino acids with a C2-symmetric homoditopic receptor
-
Sambasivan S, Kim D, Ahn KH (2010) Chiral discrimination of α-amino acids with a C2-symmetric homoditopic receptor. Chem Commun 46: 541-543
-
(2010)
Chem Commun
, vol.46
, pp. 541-543
-
-
Sambasivan, S.1
Kim, D.2
Ahn, K.H.3
-
94
-
-
76449097980
-
Synthesis, resolution and absolute configuration of 4-amino-3- phenylpiperidine
-
Schramm H, Christoffers J (2009) Synthesis, resolution and absolute configuration of 4-amino-3-phenylpiperidine. Tetrahedron Asymmetry 20: 2724-2727
-
(2009)
Tetrahedron Asymmetry
, vol.20
, pp. 2724-2727
-
-
Schramm, H.1
Christoffers, J.2
-
95
-
-
62749156477
-
New chiral derivatizing agents: Convenient determination of absolute configurations of free amino acids by 1H NMR
-
Kurosu M, Li K (2009) New chiral derivatizing agents: convenient determination of absolute configurations of free amino acids by 1H NMR. Org Lett 11: 911-914
-
(2009)
Org Lett
, vol.11
, pp. 911-914
-
-
Kurosu, M.1
Li, K.2
-
96
-
-
0002042160
-
Phospho-transfer catalysis. on the asymmetric hydrophosphonylation of aldehydes
-
Davies SR, Mitchell MC, Cain CP, Devitt PG, Taylor RJ, Kee TP (1998) Phospho-transfer catalysis. On the asymmetric hydrophosphonylation of aldehydes. J Organomet Chem 550: 29-57
-
(1998)
J Organomet Chem
, vol.550
, pp. 29-57
-
-
Davies, S.R.1
Mitchell, M.C.2
Cain, C.P.3
Devitt, P.G.4
Taylor, R.J.5
Kee, T.P.6
-
97
-
-
0002006360
-
New methodologies for enantiomeric excess (ee) determination based on phosphorus NMR
-
Hulst R, Kellogg RM, Feringa BL (1995) New methodologies for enantiomeric excess (ee) determination based on phosphorus NMR. Recl Trav Chim Pays-Bas 114: 115-138
-
(1995)
Recl Trav Chim Pays-Bas
, vol.114
, pp. 115-138
-
-
Hulst, R.1
Kellogg, R.M.2
Feringa, B.L.3
-
98
-
-
43149117690
-
Phosphoroselenoic acid derivatives bearing a binaphthyl group as a chiral molecular tool
-
Murai T (2008) Phosphoroselenoic acid derivatives bearing a binaphthyl group as a chiral molecular tool. Phosphorus Sulfur Silicon 189: 889-896
-
(2008)
Phosphorus Sulfur Silicon
, vol.189
, pp. 889-896
-
-
Murai, T.1
-
99
-
-
77951581521
-
Assignment of the absolute configurations of 1-aryl-2-propanols with the use of phosphoroselenoyl chlorides as chiral derivatizing agents
-
Murai T, Tsuji H, Imaizumi S, Maruyama T (2010) Assignment of the absolute configurations of 1-aryl-2-propanols with the use of phosphoroselenoyl chlorides as chiral derivatizing agents. Chem Lett 39: 524-526
-
(2010)
Chem Lett
, vol.39
, pp. 524-526
-
-
Murai, T.1
Tsuji, H.2
Imaizumi, S.3
Maruyama, T.4
-
100
-
-
62849099013
-
31P NMR assays for rapid determination of enantiomeric excess in catalytic hydrosilylations and transfer hydrogenations
-
Reiner T, Naraschewski FN, Eppinger J (2009) 31P NMR assays for rapid determination of enantiomeric excess in catalytic hydrosilylations and transfer hydrogenations. Tetrahedron Asymmetry 20: 362-367
-
(2009)
Tetrahedron Asymmetry
, vol.20
, pp. 362-367
-
-
Reiner, T.1
Naraschewski, F.N.2
Eppinger, J.3
-
101
-
-
43449084642
-
2-Chloro-(4R,5R)-bis[(1R,2S,5R)- menth-1-yloxycarbonyl)]-1,3,2- dioxaphospholane: A practical chiral pool-derived reagent for determining enantiomeric purity of alcohols
-
Amberg M, Bergstrasser U, Stapf G, Hartung J (2008) 2-Chloro-(4R,5R)- bis[(1R,2S,5R)- menth-1-yloxycarbonyl)]-1,3,2-dioxaphospholane: a practical chiral pool-derived reagent for determining enantiomeric purity of alcohols. J Org Chem 73: 3907-3910
-
(2008)
J Org Chem
, vol.73
, pp. 3907-3910
-
-
Amberg, M.1
Bergstrasser, U.2
Stapf, G.3
Hartung, J.4
-
102
-
-
79959327326
-
Derivatizing agents from phosphorus trichloride and terpenyl tartrates for determining enantiomeric purity of alcohols
-
Amberg M, Kempter I, Bergstrasser U, Stapf G, Hartung J (2011) Derivatizing agents from phosphorus trichloride and terpenyl tartrates for determining enantiomeric purity of alcohols. Tetrahedron Asymmetry 22: 752-760
-
(2011)
Tetrahedron Asymmetry
, vol.22
, pp. 752-760
-
-
Amberg, M.1
Kempter, I.2
Bergstrasser, U.3
Stapf, G.4
Hartung, J.5
-
103
-
-
34250214123
-
Determination of the enantiomeric excess of chiral carboxylic acids by 31P NMR with phosphorylated derivatizing agents from C2-symmetrical diamines containing the (S)-α-phenylethyl group
-
Mastranzo VM, Quintero L, De Parrodi CA (2007) Determination of the enantiomeric excess of chiral carboxylic acids by 31P NMR with phosphorylated derivatizing agents from C2-symmetrical diamines containing the (S)-α-phenylethyl group. Chirality 19: 503-507
-
(2007)
Chirality
, vol.19
, pp. 503-507
-
-
Mastranzo, V.M.1
Quintero, L.2
De Parrodi, C.A.3
-
104
-
-
39449139629
-
Simple protocols for NMR analysis of the enantiomeric purity of chiral primary amines
-
Perez-Fuertes Y, Kelly AM, Fossey JS, Powell ME, Bull SD, James TD (2008) Simple protocols for NMR analysis of the enantiomeric purity of chiral primary amines. Nat Protoc 3: 210-214
-
(2008)
Nat Protoc
, vol.3
, pp. 210-214
-
-
Perez-Fuertes, Y.1
Kelly, A.M.2
Fossey, J.S.3
Powell, M.E.4
Bull, S.D.5
James, T.D.6
-
105
-
-
39949083373
-
Simple chiral derivatisation protocols for NMR analysis of the enantiopurity of 1,2-diphenylethane-1,2-diamine and N-Boc-cyclohexane- 1,2-diamine
-
Kelly AM, Bull SD, James TD (2008) Simple chiral derivatisation protocols for NMR analysis of the enantiopurity of 1,2-diphenylethane-1,2-diamine and N-Boc-cyclohexane- 1,2-diamine. Tetrahedron Asymmetry 19: 489-494
-
(2008)
Tetrahedron Asymmetry
, vol.19
, pp. 489-494
-
-
Kelly, A.M.1
Bull, S.D.2
James, T.D.3
-
106
-
-
33644773399
-
Simple protocol for NMR analysis of the enantiomeric purity of primary amines
-
Perez-Fuertes Y, Kelly AM, Johnson AL, Arimori S, Bull SD, James TD (2006) Simple protocol for NMR analysis of the enantiomeric purity of primary amines. Org Lett 8: 609-612
-
(2006)
Org Lett
, vol.8
, 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
-
107
-
-
39449120441
-
Simple protocols for NMR analysis of the enantiomeric purity of chiral diols
-
Kelly AM, Perez-Fuertes Y, Fossey JS, Yeste SL, Bull SD, James TD (2008) Simple protocols for NMR analysis of the enantiomeric purity of chiral diols. Nat Protoc 3: 215-219
-
(2008)
Nat Protoc
, vol.3
, pp. 215-219
-
-
Kelly, A.M.1
Perez-Fuertes, Y.2
Fossey, J.S.3
Yeste, S.L.4
Bull, S.D.5
James, T.D.6
-
108
-
-
58149280401
-
Simple chiral derivatization protocols for 1H NMR and 19F NMR spectroscopic analysis of the enantiopurity of chiral diols
-
Yeste SL, Powell ME, Bull SD, James TD (2009) Simple chiral derivatization protocols for 1H NMR and 19F NMR spectroscopic analysis of the enantiopurity of chiral diols. J Org Chem 74: 427-430
-
(2009)
J Org Chem
, vol.74
, pp. 427-430
-
-
Yeste, S.L.1
Powell, M.E.2
Bull, S.D.3
James, T.D.4
-
109
-
-
84855522121
-
Three-component chiral derivatizing protocols for NMR spectroscopic enantiodiscrimination of hydroxyl acids and primary amines
-
Chaudhari SR, Suryaprakash N (2012) Three-component chiral derivatizing protocols for NMR spectroscopic enantiodiscrimination of hydroxyl acids and primary amines. J Org Chem 77: 648-651
-
(2012)
J Org Chem
, vol.77
, pp. 648-651
-
-
Chaudhari, S.R.1
Suryaprakash, N.2
-
110
-
-
84863953428
-
Simple and efficient methods for discrimination of chiral diacids and chiral alpha-methyl amines
-
Chaudhari SR, Suryaprakash N (2012) Simple and efficient methods for discrimination of chiral diacids and chiral alpha-methyl amines. Org Biomol Chem 10: 6410-6419
-
(2012)
Org Biomol Chem
, vol.10
, pp. 6410-6419
-
-
Chaudhari, S.R.1
Suryaprakash, N.2
-
111
-
-
58149334774
-
A simple chiral derivatisation protocol for 1H NMR spectroscopic analysis of the enantiopurity of O-silyl-1,2-amino alcohols
-
Powell ME, Kelly AM, Bull SD, James TD (2009) A simple chiral derivatisation protocol for 1H NMR spectroscopic analysis of the enantiopurity of O-silyl-1,2-amino alcohols. Tetrahedron Lett 50: 876-879
-
(2009)
Tetrahedron Lett
, vol.50
, pp. 876-879
-
-
Powell, M.E.1
Kelly, A.M.2
Bull, S.D.3
James, T.D.4
-
112
-
-
52049084094
-
In tube determination of the absolute configuration of α- And β-hydroxy acids by NMR via chiral BINOL borates
-
Freire F, Quinoa E, Riguera R (2008) In tube determination of the absolute configuration of α- and β-hydroxy acids by NMR via chiral BINOL borates. Chem Commun 44: 4147-4149
-
(2008)
Chem Commun
, vol.44
, pp. 4147-4149
-
-
Freire, F.1
Quinoa, E.2
Riguera, R.3
-
113
-
-
43249090061
-
Determination of absolute configuration of conformationally flexible cis-dihydrodiol metabolites: Effect of diene substitution pattern on the circular dichroism spectra and optical rotations
-
Kwit M, Sharma ND, Boyd DR, Gawronski J (2008) Determination of absolute configuration of conformationally flexible cis-dihydrodiol metabolites: effect of diene substitution pattern on the circular dichroism spectra and optical rotations. Chirality 20: 609-620
-
(2008)
Chirality
, vol.20
, pp. 609-620
-
-
Kwit, M.1
Sharma, N.D.2
Boyd, D.R.3
Gawronski, J.4
-
114
-
-
34547212769
-
Enzyme-catalysed synthesis and absolute configuration assignments of cis-dihydrodiol metabolites from 1,4- disubstituted benzenes
-
Boyd DR, Sharma ND, Coen GP, Gray PJ, Malone JF, Gawronski J (2007) Enzyme-catalysed synthesis and absolute configuration assignments of cis-dihydrodiol metabolites from 1,4- disubstituted benzenes. Chem Eur J 13: 5804-5811
-
(2007)
Chem Eur J
, vol.13
, pp. 5804-5811
-
-
Boyd, D.R.1
Sharma, N.D.2
Coen, G.P.3
Gray, P.J.4
Malone, J.F.5
Gawronski, J.6
-
115
-
-
70349146708
-
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 (2009) Pattern-based recognition for the rapid determination of identity, concentration, and enantiomeric excess of subtly different threo diols. J Am Chem Soc 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
-
116
-
-
78649619442
-
Enantiomeric excess detection with (S)-3-phenyl-2- (selenophenyl)propan- 1-ol derivatizing agent via mix and shake 77Se NMR
-
Ferreira JG, Goncalves SMC (2010) Enantiomeric excess detection with (S)-3-phenyl-2- (selenophenyl)propan-1-ol derivatizing agent via mix and shake 77Se NMR. J Braz Chem Soc 21: 2023-2026
-
(2010)
J Braz Chem Soc
, vol.21
, pp. 2023-2026
-
-
Ferreira, J.G.1
Goncalves, S.M.C.2
-
117
-
-
77951834913
-
First principles design of derivatizing agent for direct determination of enantiomeric purity of chiral alcohols and amines by NMR spectroscopy
-
Orlov NV, Ananikov VP (2010) First principles design of derivatizing agent for direct determination of enantiomeric purity of chiral alcohols and amines by NMR spectroscopy. Chem Commun 46: 3212-3214
-
(2010)
Chem Commun
, vol.46
, pp. 3212-3214
-
-
Orlov, N.V.1
Ananikov, V.P.2
-
118
-
-
1642331562
-
Sulfated and carboxymethylated cyclodextrins and their lanthanide complexes as chiral NMR differentiating agents
-
Wenzel TJ, Amoono EP, Shariff SS, Aniagyei SE (2003) Sulfated and carboxymethylated cyclodextrins and their lanthanide complexes as chiral NMR differentiating agents. Tetrahedron Asymmetry 14: 3099-3104
-
(2003)
Tetrahedron Asymmetry
, vol.14
, pp. 3099-3104
-
-
Wenzel, T.J.1
Amoono, E.P.2
Shariff, S.S.3
Aniagyei, S.E.4
-
119
-
-
33646832200
-
Carboxymethylated cyclodextrin derivatives as chiral NMR differentiating agents
-
Dignam CF, Randall LA, Blacken RD, Cunningham PR, Lester SG, Brown MJ, French SC, Aniagyei SE, Wenzel TJ (2006) Carboxymethylated cyclodextrin derivatives as chiral NMR differentiating agents. Tetrahedron Asymmetry 17: 1199-1208
-
(2006)
Tetrahedron Asymmetry
, vol.17
, pp. 1199-1208
-
-
Dignam, C.F.1
Randall, L.A.2
Blacken, R.D.3
Cunningham, P.R.4
Lester, S.G.5
Brown, M.J.6
French, S.C.7
Aniagyei, S.E.8
Wenzel, T.J.9
-
120
-
-
49049101458
-
Carboxymethylated cyclodextrins and their paramagnetic lanthanide complexes as water-soluble chiral NMR solvating agents
-
Provencher KA, Wenzel TJ (2008) Carboxymethylated cyclodextrins and their paramagnetic lanthanide complexes as water-soluble chiral NMR solvating agents. Tetrahedron Asymmetry 19: 1797-1803
-
(2008)
Tetrahedron Asymmetry
, vol.19
, pp. 1797-1803
-
-
Provencher, K.A.1
Wenzel, T.J.2
-
121
-
-
75849142250
-
Carboxymethylated cyclodextrins and their complexes with Pr(III) and Yb(III) as watersoluble chiral NMR solvating agents for cationic compounds
-
Provencher KA, Weber MA, Randall LA, Cunningham PR, Dignam CF, Wenzel TJ (2010) Carboxymethylated cyclodextrins and their complexes with Pr(III) and Yb(III) as watersoluble chiral NMR solvating agents for cationic compounds. Chirality 22: 336-346
-
(2010)
Chirality
, vol.22
, pp. 336-346
-
-
Provencher, K.A.1
Weber, M.A.2
Randall, L.A.3
Cunningham, P.R.4
Dignam, C.F.5
Wenzel, T.J.6
-
122
-
-
0028129338
-
Lanthanide-cyclodextrin complexes as probes for elucidating optical purity by NMR spectroscopy
-
Wenzel TJ, Bogyo MS, Lebeau EL (1994) Lanthanide-cyclodextrin complexes as probes for elucidating optical purity by NMR spectroscopy. J Am Chem Soc 116: 4858-4865
-
(1994)
J Am Chem Soc
, vol.116
, pp. 4858-4865
-
-
Wenzel, T.J.1
Bogyo, M.S.2
Lebeau, E.L.3
-
123
-
-
0033966864
-
Dysprosium(III)-diethylenetriaminepentaacetate complexes of aminocyclodextrins as chiral NMR shift reagents
-
Wenzel TJ, Miles RD, Zomlefer K, Frederique DE, Roan MA, Troughton JS, Pond BV, Colby AL (2000) Dysprosium(III)-diethylenetriaminepentaacetate complexes of aminocyclodextrins as chiral NMR shift reagents. Chirality 12: 30-37
-
(2000)
Chirality
, vol.12
, pp. 30-37
-
-
Wenzel, T.J.1
Miles, R.D.2
Zomlefer, K.3
Frederique, D.E.4
Roan, M.A.5
Troughton, J.S.6
Pond, B.V.7
Colby, A.L.8
-
124
-
-
10744222472
-
Calix[4]arene, calix[4]resorcarene, and cyclodextrin derivatives and their lanthanide complexes as chiral NMR shift reagents
-
Smith KJ, Wilcox JD,Mirick GE, Wacker LS, Ryan NS, Vensel DA, Readling R, Domush HL, Amonoo EP, Shariff SS, Wenzel TJ (2003) Calix[4]arene, calix[4]resorcarene, and cyclodextrin derivatives and their lanthanide complexes as chiral NMR shift reagents. Chirality 15:S150-S158
-
(2003)
Chirality
, vol.15
-
-
Smith, K.J.1
Wilcox Jdmirick, G.E.2
Wacker, L.S.3
Ryan, N.S.4
Vensel, D.A.5
Readling, R.6
Domush, H.L.7
Amonoo, E.P.8
Shariff, S.S.9
Wenzel, T.J.10
-
125
-
-
79951810670
-
Enantiomeric discrimination of aromatic-containing anionic substrates using cationic cyclodextrins
-
Chisholm CD, Wenzel TJ (2011) Enantiomeric discrimination of aromatic-containing anionic substrates using cationic cyclodextrins. Tetrahedron Asymmetry 22: 62-68
-
(2011)
Tetrahedron Asymmetry
, vol.22
, pp. 62-68
-
-
Chisholm, C.D.1
Wenzel, T.J.2
-
126
-
-
33845558509
-
Host-guest complexation. 23. High chiral recognition of amino acid and ester guests by hosts containing one chiral element
-
Lingenfelter DS, Helgeson RC, Cram DJ (1981) Host-guest complexation. 23. High chiral recognition of amino acid and ester guests by hosts containing one chiral element. J Org Chem 46: 393-406
-
(1981)
J Org Chem
, vol.46
, pp. 393-406
-
-
Lingenfelter, D.S.1
Helgeson, R.C.2
Cram, D.J.3
-
127
-
-
0031502358
-
Lanthanide-crown ether mixtures as chiral NMR shift reagents for amino acid esters, amines and amino alcohols
-
Weinstein SE, Vining MS, Wenzel TJ (1997) Lanthanide-crown ether mixtures as chiral NMR shift reagents for amino acid esters, amines and amino alcohols. Magn Reson Chem 35: 273-280
-
(1997)
Magn Reson Chem
, vol.35
, pp. 273-280
-
-
Weinstein, S.E.1
Vining, M.S.2
Wenzel, T.J.3
-
128
-
-
0035926483
-
Utility of crown ethers derived from methyl β-D-galactopyranoside and their lanthanide couples as chiral NMR discriminating agents
-
Wenzel TJ, Thurston JE, Sek DC, Joly J (2001) Utility of crown ethers derived from methyl β-D-galactopyranoside and their lanthanide couples as chiral NMR discriminating agents. Tetrahedron Asymmetry 12: 1125-1130
-
(2001)
Tetrahedron Asymmetry
, vol.12
, pp. 1125-1130
-
-
Wenzel, T.J.1
Thurston, J.E.2
Sek, D.C.3
Joly, J.4
-
129
-
-
17044414671
-
Chiral recognition in NMR spectroscopy using crown ethers and their ytterbium(III) complexes
-
Wenzel TJ, Freeman BE, Sek DC, Zopf JJ, Nakamura T, Yongzhu J, Hirose K, Tobe Y (2004) Chiral recognition in NMR spectroscopy using crown ethers and their ytterbium(III) complexes. Anal Bioanal Chem 378: 1536-1547
-
(2004)
Anal Bioanal Chem
, vol.378
, pp. 1536-1547
-
-
Wenzel, T.J.1
Freeman, B.E.2
Sek, D.C.3
Zopf, J.J.4
Nakamura, T.5
Yongzhu, J.6
Hirose, K.7
Tobe, Y.8
-
130
-
-
0034629087
-
(+)-(18-Crown-6)-2,3,11,12-tetracarboxylic acid and its ytterbium(III) complex as chiral NMR discriminating agents
-
Wenzel TJ, Thurston JE (2000) (+)-(18-Crown-6)-2,3,11,12-tetracarboxylic acid and its ytterbium(III) complex as chiral NMR discriminating agents. J Org Chem 65: 1243-1248
-
(2000)
J Org Chem
, vol.65
, pp. 1243-1248
-
-
Wenzel, T.J.1
Thurston, J.E.2
-
131
-
-
0034697459
-
Enantiomeric discrimination in the NMR spectra of underivatized amino acids and α-methyl amino acids using (+)-(18-crown-6)-2,3,11,12- tetracarboxylic acid
-
Wenzel TJ, Thurston JE (2000) Enantiomeric discrimination in the NMR spectra of underivatized amino acids and α-methyl amino acids using (+)-(18-crown-6)-2,3,11,12- tetracarboxylic acid. Tetrahedron Lett 41: 3769-3772
-
(2000)
Tetrahedron Lett
, vol.41
, pp. 3769-3772
-
-
Wenzel, T.J.1
Thurston, J.E.2
-
132
-
-
0037437690
-
Nuclear magnetic resonance studies for the chiral recognition of (+)-(R)-18-crown-6-tetracarboxylic acid to amino compounds
-
Machida Y, Kagawa M, Nishi H (2003) Nuclear magnetic resonance studies for the chiral recognition of (+)-(R)-18-crown-6-tetracarboxylic acid to amino compounds. J Pharm Biomed Anal 30: 1929-1942
-
(2003)
J Pharm Biomed Anal
, vol.30
, pp. 1929-1942
-
-
Machida, Y.1
Kagawa, M.2
Nishi, H.3
-
133
-
-
70349223813
-
(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 (2009) (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 20: 2052-2060
-
(2009)
Tetrahedron Asymmetry
, vol.20
, pp. 2052-2060
-
-
Wenzel, T.J.1
Bourne, C.E.2
Clark, R.L.3
-
134
-
-
77957120035
-
Enantiomeric discrimination of cyclic β-amino acids using (18-crown-6)-2,3,11,12-tetracarboxylic acid as a chiral NMR solvating agent
-
Chisholm CD, Fulop F, Forro E, Wenzel TJ (2010) Enantiomeric discrimination of cyclic β-amino acids using (18-crown-6)-2,3,11,12- tetracarboxylic acid as a chiral NMR solvating agent. Tetrahedron Asymmetry 21: 2289-2294
-
(2010)
Tetrahedron Asymmetry
, vol.21
, pp. 2289-2294
-
-
Chisholm, C.D.1
Fulop, F.2
Forro, E.3
Wenzel, T.J.4
-
135
-
-
84871614873
-
Enantiomeric discrimination of isoxazoline fused β-amino acid derivatives using (18-crown-6)-2,3,11,12-tetracarboxylic acid as a chiral NMR solvating agent
-
Howard JA, Fulop F, Nonn M, Wenzel TJ (2013) Enantiomeric discrimination of isoxazoline fused β-amino acid derivatives using (18-crown-6)-2,3,11,12- tetracarboxylic acid as a chiral NMR solvating agent. Chirality 25: 48-53
-
(2013)
Chirality
, vol.25
, pp. 48-53
-
-
Howard, J.A.1
Fulop, F.2
Nonn, M.3
Wenzel, T.J.4
-
136
-
-
33746163942
-
Chiral NMR discrimination of secondary amines using (18-crown-6)-2,3,11, 12-tetracarboxylic acid
-
Lovely AE, Wenzel TJ (2006) Chiral NMR discrimination of secondary amines using (18-crown-6)-2,3,11,12-tetracarboxylic acid. Org Lett 8: 2823-2826
-
(2006)
Org Lett
, vol.8
, pp. 2823-2826
-
-
Lovely, A.E.1
Wenzel, T.J.2
-
137
-
-
33751555211
-
Chiral NMR discrimination of piperidines and piperazines using (18-crown-6)2,3,11,12-tetracarboxylic acid
-
Lovely AE, Wenzel TJ (2006) Chiral NMR discrimination of piperidines and piperazines using (18-crown-6)2,3,11,12-tetracarboxylic acid. J Org Chem 71: 9178-9182
-
(2006)
J Org Chem
, vol.71
, pp. 9178-9182
-
-
Lovely, A.E.1
Wenzel, T.J.2
-
138
-
-
33750506076
-
Chiral NMR discrimination of pyrrolidines using (18-crown-6)- 2,3,11,12-tetracarboxylic acid
-
Lovely AE,Wenzel TJ (2006) Chiral NMR discrimination of pyrrolidines using (18-crown-6)- 2,3,11,12-tetracarboxylic acid. Tetrahedron Asymmetry 17: 2642-2648
-
(2006)
Tetrahedron Asymmetry
, vol.17
, pp. 2642-2648
-
-
Lovely Aewenzel, T.J.1
-
139
-
-
39749202875
-
Chiral NMR discrimination of amines: Analysis of secondary, tertiary and prochiral amines using (18-crown-6)-2,3,11,12-tetracarboxylic acid
-
Lovely AE, Wenzel TJ (2008) Chiral NMR discrimination of amines: analysis of secondary, tertiary and prochiral amines using (18-crown-6)-2,3,11,12- tetracarboxylic acid. Chirality 20: 370-378
-
(2008)
Chirality
, vol.20
, pp. 370-378
-
-
Lovely, A.E.1
Wenzel, T.J.2
-
140
-
-
0001446114
-
Chiral host-guest interaction. A water-soluble calix[4]resorcarene having L-proline moieties as a non-lanthanide chiral NMR shift reagent for chiral aromatic guests in water
-
Yanagihara R, Tominaga M, Aoyama Y (1994) Chiral host-guest interaction. A water-soluble calix[4]resorcarene having L-proline moieties as a non-lanthanide chiral NMR shift reagent for chiral aromatic guests in water. J Org Chem 59: 6865-6867
-
(1994)
J Org Chem
, vol.59
, pp. 6865-6867
-
-
Yanagihara, R.1
Tominaga, M.2
Aoyama, Y.3
-
141
-
-
18844378094
-
An enantioselective NMR shift reagent for cationic aromatics
-
Dignam CF, Richards CJ, Zopf JJ, Wacker LS, Wenzel TJ (2005) An enantioselective NMR shift reagent for cationic aromatics. Org Lett 7: 1773-1776
-
(2005)
Org Lett
, vol.7
, pp. 1773-1776
-
-
Dignam, C.F.1
Richards, C.J.2
Zopf, J.J.3
Wacker, L.S.4
Wenzel, T.J.5
-
142
-
-
25444445878
-
Water-soluble calix[4]resorcarenes as enantioselective NMR shift reagents for aromatic compounds
-
Dignam CF, Zopf JJ, Richards CJ, Wenzel TJ (2005) Water-soluble calix[4]resorcarenes as enantioselective NMR shift reagents for aromatic compounds. J Org Chem 70: 8071-8078
-
(2005)
J Org Chem
, vol.70
, pp. 8071-8078
-
-
Dignam, C.F.1
Zopf, J.J.2
Richards, C.J.3
Wenzel, T.J.4
-
143
-
-
70350548550
-
Water-soluble calix[4]resorcinarenes as chiral NMR solvating agents for bicyclic aromatic compounds
-
O'Farrell CM, Hagan KA, Wenzel TJ (2009) Water-soluble calix[4]resorcinarenes as chiral NMR solvating agents for bicyclic aromatic compounds. Chirality 21: 911-921
-
(2009)
Chirality
, vol.21
, pp. 911-921
-
-
O'Farrell, C.M.1
Hagan, K.A.2
Wenzel, T.J.3
-
144
-
-
70349335248
-
Water-soluble calix[4]resorcinarenes with hydroxyproline groups as chiral NMR solvating agents for phenyl- and pyridyl-containing compounds
-
Hagan KA, O'Farrell CM, Wenzel TJ (2009) Water-soluble calix[4]resorcinarenes with hydroxyproline groups as chiral NMR solvating agents for phenyl- and pyridyl-containing compounds. Eur J Org Chem 2009: 4825-4832
-
(2009)
Eur J Org Chem
, vol.2009
, pp. 4825-4832
-
-
Hagan, K.A.1
O'Farrell, C.M.2
Wenzel, T.J.3
-
145
-
-
49049117088
-
Water-soluble calix[4]resorcinarenes as chiral NMR solvating agents for phenyl-containing compounds
-
O'Farrell CM, Wenzel TJ (2008) Water-soluble calix[4]resorcinarenes as chiral NMR solvating agents for phenyl-containing compounds. Tetrahedron Asymmetry 19: 1790-1796
-
(2008)
Tetrahedron Asymmetry
, vol.19
, pp. 1790-1796
-
-
O'Farrell, C.M.1
Wenzel, T.J.2
-
146
-
-
41649087625
-
Water-soluble calix [4]resorcinarenes with hydroxyproline groups as chiral NMR solvating agents
-
O'Farrell CM, Chudomel JM, Collins JM, Dignam CF, Wenzel TJ (2008) Water-soluble calix [4]resorcinarenes with hydroxyproline groups as chiral NMR solvating agents. J Org Chem 73: 2843-2851
-
(2008)
J Org Chem
, vol.73
, pp. 2843-2851
-
-
O'Farrell, C.M.1
Chudomel, J.M.2
Collins, J.M.3
Dignam, C.F.4
Wenzel, T.J.5
-
147
-
-
79851503897
-
A water-soluble calix[4]resorcinarene with α-methyl-Lprolinylmethyl groups as a chiral NMR solvating agent
-
Pham NH, Wenzel TJ (2011) A water-soluble calix[4]resorcinarene with α-methyl-Lprolinylmethyl groups as a chiral NMR solvating agent. J Org Chem 76: 986-989
-
(2011)
J Org Chem
, vol.76
, pp. 986-989
-
-
Pham, N.H.1
Wenzel, T.J.2
-
148
-
-
79956357843
-
A sulfonated calix[4]resorcinarene with α-methyl-Lprolinylmethyl groups as a water-soluble chiral NMR solvating agent
-
Pham NH, Wenzel TJ (2011) A sulfonated calix[4]resorcinarene with α-methyl-Lprolinylmethyl groups as a water-soluble chiral NMR solvating agent. Tetrahedron Asymmetry 22: 641-647
-
(2011)
Tetrahedron Asymmetry
, vol.22
, pp. 641-647
-
-
Pham, N.H.1
Wenzel, T.J.2
-
149
-
-
80054938801
-
A sulfonated calix[4]resorcinarene with L-pipecolinic acid groups as a water-soluble chiral NMR solvating agent
-
Pham NH, Wenzel TJ (2011) A sulfonated calix[4]resorcinarene with L-pipecolinic acid groups as a water-soluble chiral NMR solvating agent. Tetrahedron Asymmetry 22: 1574-1580
-
(2011)
Tetrahedron Asymmetry
, vol.22
, pp. 1574-1580
-
-
Pham, N.H.1
Wenzel, T.J.2
-
150
-
-
84857358961
-
A water-soluble calix[4]resorcinarene with L-pipecolinic acid groups as a chiral NMR solvating agent
-
Pham NH, Wenzel TJ (2012) A water-soluble calix[4]resorcinarene with L-pipecolinic acid groups as a chiral NMR solvating agent. Chirality 24: 193-200
-
(2012)
Chirality
, vol.24
, pp. 193-200
-
-
Pham, N.H.1
Wenzel, T.J.2
-
151
-
-
84859424571
-
Chiral discrimination of aliphatic amines and amino alcohols using NMR spectroscopy
-
Wenzel TJ, Rollo RD, Clark RL (2012) Chiral discrimination of aliphatic amines and amino alcohols using NMR spectroscopy. Magn Reson Chem 50: 261-265
-
(2012)
Magn Reson Chem
, vol.50
, pp. 261-265
-
-
Wenzel, T.J.1
Rollo, R.D.2
Clark, R.L.3
-
152
-
-
33947291797
-
Tris[3-(trifluoromethylhydroxymethylene)- d-camphorato]europium(III). A chiral shift reagent for direct determination of enantiomeric compositions
-
Goering HL, Eikenberry JN, Koermer GS (1971) Tris[3- (trifluoromethylhydroxymethylene)- d-camphorato]europium(III). A chiral shift reagent for direct determination of enantiomeric compositions. J Am Chem Soc 93: 5913-5914
-
(1971)
J Am Chem Soc
, vol.93
, pp. 5913-5914
-
-
Goering, H.L.1
Eikenberry, J.N.2
Koermer, G.S.3
-
153
-
-
37049121001
-
Determination of enantiomeric purity by an optically active nuclear magnetic resonance shift reagent of wide applicability
-
Fraser RR, Petit MA, Saunders JK (1971) Determination of enantiomeric purity by an optically active nuclear magnetic resonance shift reagent of wide applicability. Chem Commun 1450-1451
-
(1971)
Chem Commun
, pp. 1450-1451
-
-
Fraser, R.R.1
Petit, M.A.2
Saunders, J.K.3
-
154
-
-
0001166795
-
The determination of enantiomeric purity using chiral lanthanide shift reagents
-
McCreary MD, Lewis DW, Wernick DL, Whitesides GM (1974) The determination of enantiomeric purity using chiral lanthanide shift reagents. J Am Chem Soc 96: 1038-1054
-
(1974)
J Am Chem Soc
, vol.96
, pp. 1038-1054
-
-
McCreary, M.D.1
Lewis, D.W.2
Wernick, D.L.3
Whitesides, G.M.4
-
156
-
-
84896972436
-
Lanthanide enolates as nuclear magnetic resonance shift reagents
-
Abicky J (ed) Wiley, West Sussex
-
Wenzel TJ, Provencher KA (2009) Lanthanide enolates as nuclear magnetic resonance shift reagents. In: Abicky J (ed) The chemistry of metal enolates. Wiley, West Sussex, p 788-822
-
(2009)
The Chemistry of Metal Enolates
, pp. 788-822
-
-
Wenzel, T.J.1
Provencher, K.A.2
-
157
-
-
0000926958
-
Determination of enantiomeric purity of polar substrates with chiral lanthanide NMR shift reagents in polar solvents
-
Sweeting LM, Crans DC, Whitesides GM (1987) Determination of enantiomeric purity of polar substrates with chiral lanthanide NMR shift reagents in polar solvents. J Org Chem 52: 2273-2276
-
(1987)
J Org Chem
, vol.52
, pp. 2273-2276
-
-
Sweeting, L.M.1
Crans, D.C.2
Whitesides, G.M.3
-
158
-
-
0038007255
-
NMR studies of drugs. Application of a chiral lanthanide shift reagent to methoxamine in chloroform-d or acetonitrile-d3
-
DeArment M, Eastabrooks M, Venkatasubban KS, Benshafrut R, Rothchild R, Wyss H (1994) NMR studies of drugs. Application of a chiral lanthanide shift reagent to methoxamine in chloroform-d or acetonitrile-d3. Spectrosc Lett 27: 533-555
-
(1994)
Spectrosc Lett
, vol.27
, pp. 533-555
-
-
Dearment, M.1
Eastabrooks, M.2
Venkatasubban, K.S.3
Benshafrut, R.4
Rothchild, R.5
Wyss, H.6
-
159
-
-
0006062073
-
4H-Benzo[4,5]cyclohepta[1,2-b]thiophenes and 9,10- dihydro derivatives - Sulfonium analogues of pizotifen and ketotifen; Chirality of ketotifen; Synthesis of the 2-bromo derivative of ketotifen
-
Polivka Z, Budesínsky M, Holubek J, Schneider B, Sedivy Z, Svatek E, Matousova O,Metys J, Valchar M, Soucek R, Protiva M (1989) 4H-Benzo[4,5]cyclohepta[1,2-b]thiophenes and 9,10- dihydro derivatives - sulfonium analogues of pizotifen and ketotifen; chirality of ketotifen; synthesis of the 2-bromo derivative of ketotifen. Collect Czech Chem Commun 54: 2443-2469
-
(1989)
Collect Czech Chem Commun
, vol.54
, pp. 2443-2469
-
-
Polivka, Z.1
Budesínsky, M.2
Holubek, J.3
Schneider, B.4
Sedivy, Z.5
Svatek, E.6
Matousova Ometys, J.7
Valchar, M.8
Soucek, R.9
Protiva, M.10
-
160
-
-
4143107235
-
Observing the enantiomeric 1H chemical shift nonequivalence of several α-amino ester signals using tris[3-(trifluoromethylhydroxy-methylene)-(+)- camphorato]samarium(III): A chiral lanthanide shift reagent that causes minimal line bordering
-
Omata K, Aoyagi S, Kabuto K (2004) Observing the enantiomeric 1H chemical shift nonequivalence 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 15: 2351-2356
-
(2004)
Tetrahedron Asymmetry
, vol.15
, pp. 2351-2356
-
-
Omata, K.1
Aoyagi, S.2
Kabuto, K.3
-
161
-
-
60849122836
-
Diamagnetic lanthanide tris β-diketonates as organic-soluble chiral NMR shift reagents
-
Wenzel TJ, Wenzel BT (2009) Diamagnetic lanthanide tris β-diketonates as organic-soluble chiral NMR shift reagents. Chirality 21: 6-10
-
(2009)
Chirality
, vol.21
, pp. 6-10
-
-
Wenzel, T.J.1
Wenzel, B.T.2
-
162
-
-
84875219061
-
Diamagnetic lanthanide tris β-diketonate complexes with aryl-containing ligands as chiral NMR discriminating agents
-
Clark RL, Wenzel BT, Wenzel TJ (2013) Diamagnetic lanthanide tris β-diketonate complexes with aryl-containing ligands as chiral NMR discriminating agents. Tetrahedron Asymmetry 24: 297-304
-
(2013)
Tetrahedron Asymmetry
, vol.24
, pp. 297-304
-
-
Clark, R.L.1
Wenzel, B.T.2
Wenzel, T.J.3
-
163
-
-
11444259272
-
Application of chiral lanthanide shift reagents for assignment of absolute configuration of alcohols
-
Ghosh I, Zeng H, Kishi Y (2004) Application of chiral lanthanide shift reagents for assignment of absolute configuration of alcohols. Org Lett 6: 4715-4718
-
(2004)
Org Lett
, vol.6
, pp. 4715-4718
-
-
Ghosh, I.1
Zeng, H.2
Kishi, Y.3
-
164
-
-
55049121677
-
Determination of the absolute configuration of the glucosinolate methyl sulfoxide group reveals a stereospecific biosynthesis of the side chain
-
Vergara F, Wenzler M, Hansen BG, Kleibenstein DJ, Halkier BA, Gershenzon J, Schneider B (2008) Determination of the absolute configuration of the glucosinolate methyl sulfoxide group reveals a stereospecific biosynthesis of the side chain. Photochem 69: 2737-2742
-
(2008)
Photochem
, vol.69
, pp. 2737-2742
-
-
Vergara, F.1
Wenzler, M.2
Hansen, B.G.3
Kleibenstein, D.J.4
Halkier, B.A.5
Gershenzon, J.6
Schneider, B.7
-
165
-
-
55349107272
-
One-pot, three-component uncatalyzed quantitative synthesis of new aminonaphthols (Betti bases) in water
-
Ghandi M, Olyaei A, Raoufmoghaddam S (2008) One-pot, three-component uncatalyzed quantitative synthesis of new aminonaphthols (Betti bases) in water. Synth Commun 38: 4125-4138
-
(2008)
Synth Commun
, vol.38
, pp. 4125-4138
-
-
Ghandi, M.1
Olyaei, A.2
Raoufmoghaddam, S.3
-
166
-
-
37649033197
-
Synthesis and stereochemical stability of new atropisomeric 1-(substituted phenyl)pyrrole derivatives
-
Faigl F, Tarkanyi G, Fogassy K, Tepfenhardt D, Thurner A (2008) Synthesis and stereochemical stability of new atropisomeric 1-(substituted phenyl)pyrrole derivatives. Tetrahedron 64: 1371-1377
-
(2008)
Tetrahedron
, vol.64
, pp. 1371-1377
-
-
Faigl, F.1
Tarkanyi, G.2
Fogassy, K.3
Tepfenhardt, D.4
Thurner, A.5
-
167
-
-
79959474623
-
NMR-based enantiodifferentiation of chiral trans-2- phenylcyclopropane derivatives using a chiral lanthanide shift reagent
-
Cho NS, Kim HS, Song MS (2011) NMR-based enantiodifferentiation of chiral trans-2- phenylcyclopropane derivatives using a chiral lanthanide shift reagent. Bull Korean Chem Soc 32: 2076-2078
-
(2011)
Bull Korean Chem Soc
, vol.32
, pp. 2076-2078
-
-
Cho, N.S.1
Kim, H.S.2
Song, M.S.3
-
168
-
-
33847084961
-
New binuclear lanthanide NMR shift reagents effective for aromatic compounds
-
Wenzel TJ, Bettes TC, Sadlowski JE, Sievers RE (1980) New binuclear lanthanide NMR shift reagents effective for aromatic compounds. J Am Chem Soc 102: 5903-5904
-
(1980)
J Am Chem Soc
, vol.102
, pp. 5903-5904
-
-
Wenzel, T.J.1
Bettes, T.C.2
Sadlowski, J.E.3
Sievers, R.E.4
-
169
-
-
0000251182
-
Nuclear magnetic resonance studies of terpenes with chiral and achiral lanthanide(III)-silver(I) binuclear shift reagents
-
Wenzel TJ, Sievers RE (1982) Nuclear magnetic resonance studies of terpenes with chiral and achiral lanthanide(III)-silver(I) binuclear shift reagents. J Am Chem Soc 104: 382-388
-
(1982)
J Am Chem Soc
, vol.104
, pp. 382-388
-
-
Wenzel, T.J.1
Sievers, R.E.2
-
170
-
-
0011554228
-
Chiral recognition of alkene and arene hydrocarbons by 1H and 13C NMR. Determination of enantiomeric purity
-
Offermann W, Mannschreck A (1981) Chiral recognition of alkene and arene hydrocarbons by 1H and 13C NMR. Determination of enantiomeric purity. Tetrahedron Lett 22: 3227-3230
-
(1981)
Tetrahedron Lett
, vol.22
, pp. 3227-3230
-
-
Offermann, W.1
Mannschreck, A.2
-
171
-
-
0024489430
-
Stereochemical aspects of the "tert-amino effect". 2. Enantio and diastereoselectivity in the synthesis of quinolines, pyrrolo[1,2 a]quinolines, and [1,4]oxazino [4,3 a]quinolines
-
Nijhuis WHN, Verboom W, El-Fadl AA, van Hummel GJ, Reinhoudt DN (1989) Stereochemical aspects of the "tert-amino effect". 2. Enantio-and diastereoselectivity in the synthesis of quinolines, pyrrolo[1,2-a]quinolines, and [1,4]oxazino [4,3-a]quinolines. J Org Chem 54: 209-216
-
(1989)
J Org Chem
, vol.54
, pp. 209-216
-
-
Nijhuis, W.H.N.1
Verboom, W.2
El-Fadl, A.A.3
Van Hummel, G.J.4
Reinhoudt, D.N.5
-
172
-
-
0027492705
-
Enantioselective synthesis of chiral liquid crystalline compounds from monoterpenes
-
Wang Q, Fan SY, Wong HNC, Li Z, Fung BM, Twieg RJ, Nguyen HT (1993) Enantioselective synthesis of chiral liquid crystalline compounds from monoterpenes. Tetrahedron 49: 619-638
-
(1993)
Tetrahedron
, vol.49
, pp. 619-638
-
-
Wang, Q.1
Fan, S.Y.2
Wong, H.N.C.3
Li, Z.4
Fung, B.M.5
Twieg, R.J.6
Nguyen, H.T.7
-
173
-
-
0001369718
-
Asymmetric induction in intramolecular [2 + 2]- photocycloadditions of 1,3-disubstituted allenes with enones and enoates
-
Carreira EM, Hastings CA, Shepard MS, Yerkey LA, Millward DB (1994) Asymmetric induction in intramolecular [2 + 2]- photocycloadditions of 1,3-disubstituted allenes with enones and enoates. J Am Chem Soc 116: 6622-6630
-
(1994)
J Am Chem Soc
, vol.116
, pp. 6622-6630
-
-
Carreira, E.M.1
Hastings, C.A.2
Shepard, M.S.3
Yerkey, L.A.4
Millward, D.B.5
-
174
-
-
0001593011
-
Nuclear magnetic resonance studies of helical dipyrromethene-zinc complexes
-
Thompson A, Dolphin D (2000) Nuclear magnetic resonance studies of helical dipyrromethene-zinc complexes. Org Lett 2: 1315-1318
-
(2000)
Org Lett
, vol.2
, pp. 1315-1318
-
-
Thompson, A.1
Dolphin, D.2
-
175
-
-
0001727946
-
Lanthanide tetrakis (β-diketonates) as effective NMR shift reagents for organic salts
-
Wenzel TJ, Zaia J (1985) Lanthanide tetrakis (β-diketonates) as effective NMR shift reagents for organic salts. J Org Chem 50: 1322-1324
-
(1985)
J Org Chem
, vol.50
, pp. 1322-1324
-
-
Wenzel, T.J.1
Zaia, J.2
-
176
-
-
0000248219
-
Organic-soluble lanthanide nuclear magnetic resonance shift reagents for sulfonium and isothiouronium salts
-
Wenzel TJ, Zaia J (1987) Organic-soluble lanthanide nuclear magnetic resonance shift reagents for sulfonium and isothiouronium salts. Anal Chem 59: 562-567
-
(1987)
Anal Chem
, vol.59
, pp. 562-567
-
-
Wenzel, T.J.1
Zaia, J.2
-
177
-
-
0030882112
-
Enantiomeric purity of alkylmethylphenylsulfonium ions with chiral NMR shift reagents: Racemization by pyramidal inversion as observed by 1H NMR spectroscopy
-
Green TK, Whetstine JR, Son E (1997) Enantiomeric purity of alkylmethylphenylsulfonium ions with chiral NMR shift reagents: racemization by pyramidal inversion as observed by 1H NMR spectroscopy. Tetrahedron Asymmetry 8: 3175-3181
-
(1997)
Tetrahedron Asymmetry
, vol.8
, pp. 3175-3181
-
-
Green, T.K.1
Whetstine, J.R.2
Son, E.3
-
178
-
-
37049083982
-
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 (1987) 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 23: 670-671
-
(1987)
Chem Commun
, vol.23
, pp. 670-671
-
-
Kabuto, K.1
Sasaki, Y.2
-
179
-
-
0025133978
-
A facile NMR method for assigning absolute configuration of underivatized α-methyl-α-amino acids using a chiral lanthanoid shift reagent for aqueous solution
-
Kabuto K, Sasaki Y (1990) 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 31: 1031-1034
-
(1990)
Tetrahedron Lett
, vol.31
, pp. 1031-1034
-
-
Kabuto, K.1
Sasaki, Y.2
-
180
-
-
34548046718
-
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 (2003) Enantiomer signal separation of β-amino acids induced by Eu(III)-pdta; relation between the absolute configurations and relative shifts of enantiomer signals. Kidorui 42: 198-199
-
(2003)
Kidorui
, vol.42
, pp. 198-199
-
-
Sasaki, M.1
Omata, K.2
Kabuto, K.3
Sasaki, Y.4
-
181
-
-
0013364595
-
Optically active Ce(III) - Propylenediaminetetracetate complex: A chiral shift reagent for aqueous solution causing less signal broadening
-
Ogasawara K, Omata K, Kabuto K, Jin H, Sasaki Y (1999) Optically active Ce(III) - propylenediaminetetracetate complex: a chiral shift reagent for aqueous solution causing less signal broadening. Kidorui 34: 152-153
-
(1999)
Kidorui
, vol.34
, pp. 152-153
-
-
Ogasawara, K.1
Omata, K.2
Kabuto, K.3
Jin, H.4
Sasaki, Y.5
-
182
-
-
0000997785
-
Samarium(III)-propylenediaminetetraacetate complex: A water-soluble chiral shift reagent for use in high-field NMR
-
Inamoto A, Ogasawara K, Omata K, Kabuto K, Sasaki Y (2000) Samarium(III)-propylenediaminetetraacetate complex: a water-soluble chiral shift reagent for use in high-field NMR. Org Lett 2: 3543-3545
-
(2000)
Org Lett
, vol.2
, pp. 3543-3545
-
-
Inamoto, A.1
Ogasawara, K.2
Omata, K.3
Kabuto, K.4
Sasaki, Y.5
-
183
-
-
68149108472
-
Fast enantioselective amino acid quantitative 13C NMR determination by a praseodymium chiral shift reagent
-
Arnaud GF, Florini N, Caglioti L, Zucchi C, Palyi G (2009) Fast enantioselective amino acid quantitative 13C NMR determination by a praseodymium chiral shift reagent. Tetrahedron Asymmetry 20: 1633-1636
-
(2009)
Tetrahedron Asymmetry
, vol.20
, pp. 1633-1636
-
-
Arnaud, G.F.1
Florini, N.2
Caglioti, L.3
Zucchi, C.4
Palyi, G.5
-
184
-
-
65549123981
-
Synthesis of a water-soluble chiral NMR shift reagent: (S)-PDTA
-
Florini N, Arnaud GF, Konya B, Zucchi C, Palyi G (2009) Synthesis of a water-soluble chiral NMR shift reagent: (S)-PDTA. Tetrahedron Asymmetry 20: 1036-1039
-
(2009)
Tetrahedron Asymmetry
, vol.20
, pp. 1036-1039
-
-
Florini, N.1
Arnaud, G.F.2
Konya, B.3
Zucchi, C.4
Palyi, G.5
-
185
-
-
63049109575
-
Use of Sm(III)-{1,2-propanediamine-N,N, N0,N0-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 (2008) Use of Sm(III)-{1,2- propanediamine-N,N, N0,N0-tetra(α,α-dideuterioacetate)} complex for NMR determination of absolute configuration of each α-amino acid in peptide hydrolysate mixtures. Comm Commun 4903-4905
-
(2008)
Comm Commun
, pp. 4903-4905
-
-
Omata, K.1
Fujioka, M.2
Kabuto, K.3
Sasaki, Y.4
-
186
-
-
60849089711
-
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 (1998) Properties of chiral Ce(III)- tppn complex as a chiral shift reagent in aqueous solution. Kidorui 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
-
187
-
-
0032821574
-
Resolution of enantiomer signals by diamagnetic lanthanum(III)-N, N, N0, N0-tetrakis(2-pyridinylmethyl)-(R)-propylenediamine complex in 1H NMR
-
Sato J, Jin H, Omata K, Kabuto K, Sasaki Y (1999) Resolution of enantiomer signals by diamagnetic lanthanum(III)-N, N, N0, N0-tetrakis(2- pyridinylmethyl)-(R)-propylenediamine complex in 1H NMR. Enantiomer 4: 147-150
-
(1999)
Enantiomer
, vol.4
, pp. 147-150
-
-
Sato, J.1
Jin, H.2
Omata, K.3
Kabuto, K.4
Sasaki, Y.5
-
188
-
-
33645522790
-
Rh2[MTPA]4, a dirhodium complex as NMR auxiliary for chiral recognition
-
Duddeck H (2005) Rh2[MTPA]4, a dirhodium complex as NMR auxiliary for chiral recognition. Chem Rec 5: 1-14
-
(2005)
Chem Rec
, vol.5
, pp. 1-14
-
-
Duddeck, H.1
-
189
-
-
38949085224
-
Origin of 13C complexation shifts in the adduct formation of 2-butyl phenyl ethers with a dirhodium tetracarboxylate complex
-
Gomez ED, Duddeck H (2008) Origin of 13C complexation shifts in the adduct formation of 2-butyl phenyl ethers with a dirhodium tetracarboxylate complex. Magn Reson Chem 46: 23-29
-
(2008)
Magn Reson Chem
, vol.46
, pp. 23-29
-
-
Gomez, E.D.1
Duddeck, H.2
-
190
-
-
77149146212
-
Experimental verification of diverging mechanisms in the binding of ether, thioether, and sulfone ligands to a dirhodium tetracarboxylate
-
Mattiza JT, Meyer VJ, Duddeck H (2010) Experimental verification of diverging mechanisms in the binding of ether, thioether, and sulfone ligands to a dirhodium tetracarboxylate. Magn Reson Chem 48: 192-197
-
(2010)
Magn Reson Chem
, vol.48
, pp. 192-197
-
-
Mattiza, J.T.1
Meyer, V.J.2
Duddeck, H.3
-
191
-
-
35248900975
-
Enantiodifferentiation of polyethers by the dirhodium method. Part 2: Cyclotriveratrylenes and cryptophanes
-
Gomez ED, Brotin T, Duddeck H (2007) Enantiodifferentiation of polyethers by the dirhodium method. Part 2: cyclotriveratrylenes and cryptophanes. Tetrahedron Asymmetry 18: 2155-2164
-
(2007)
Tetrahedron Asymmetry
, vol.18
, pp. 2155-2164
-
-
Gomez, E.D.1
Brotin, T.2
Duddeck, H.3
-
192
-
-
34250737869
-
Chiral recognition of the Schiff bases by NMR spectroscopy in the presence of a chiral dirhodium complex. Deuterium isotope effect on 13C chemical shift of the optically active Schiff bases and their dirhodium adducts
-
Rozwadowski Z (2007) Chiral recognition of the Schiff bases by NMR spectroscopy in the presence of a chiral dirhodium complex. Deuterium isotope effect on 13C chemical shift of the optically active Schiff bases and their dirhodium adducts. Magn Reson Chem 45: 605-610
-
(2007)
Magn Reson Chem
, vol.45
, pp. 605-610
-
-
Rozwadowski, Z.1
-
193
-
-
52649103929
-
Chiral recognition of Schiff bases by 15N NMR spectroscopy in the presence of a dirhodium complex. Deuterium isotope effect on 15N chemical shift of the optically active Schiff bases and their dirhodium tetracarboxylate adducts
-
Rozwadowski Z, Nowak-Wydra B (2008) Chiral recognition of Schiff bases by 15N NMR spectroscopy in the presence of a dirhodium complex. Deuterium isotope effect on 15N chemical shift of the optically active Schiff bases and their dirhodium tetracarboxylate adducts. Magn Reson Chem 46: 974-978
-
(2008)
Magn Reson Chem
, vol.46
, pp. 974-978
-
-
Rozwadowski, Z.1
Nowak-Wydra, B.2
-
194
-
-
39749190069
-
Atropisomeric 3-aryl-2-oxo-4-oxazolidinones and some thione analogues - Enantiodifferentiation and ligand competition in applying the dirhodium method
-
Gomez ED, Dogan I, Yilmaz M, Demir-Ordu O, Albert D, Duddeck H (2008) Atropisomeric 3-aryl-2-oxo-4-oxazolidinones and some thione analogues - enantiodifferentiation and ligand competition in applying the dirhodium method. Chirality 20: 344-350
-
(2008)
Chirality
, vol.20
, pp. 344-350
-
-
Gomez, E.D.1
Dogan, I.2
Yilmaz, M.3
Demir-Ordu, O.4
Albert, D.5
Duddeck, H.6
-
195
-
-
40749162805
-
Chalcogen atom competition in the coordination of bicyclic β-lactam derivatives to a dirhodium tetracarboxylate complex
-
Gomez ED, Frelek J, Woznica M, Kowalska P, Jazwinski J, Duddeck H (2007) Chalcogen atom competition in the coordination of bicyclic β-lactam derivatives to a dirhodium tetracarboxylate complex. Heterocycles 74: 357-367
-
(2007)
Heterocycles
, vol.74
, pp. 357-367
-
-
Gomez, E.D.1
Frelek, J.2
Woznica, M.3
Kowalska, P.4
Jazwinski, J.5
Duddeck, H.6
-
196
-
-
79955902512
-
Adamantanes as spherical nanosondes in adducts with a chiral dirhodium complex - Discriminating enantiomers and probing spatial proximities
-
Duddeck H, Toth G, Simon A, Gomez ED, Mattiza JT (2011) Adamantanes as spherical nanosondes in adducts with a chiral dirhodium complex - discriminating enantiomers and probing spatial proximities. Magn Reson Chem 49: 326-342
-
(2011)
Magn Reson Chem
, vol.49
, pp. 326-342
-
-
Duddeck, H.1
Toth, G.2
Simon, A.3
Gomez, E.D.4
Mattiza, J.T.5
-
197
-
-
84860728748
-
Competition of ester, amide, ether, carbonate, alcohol and epoxide ligands in the dirhodium experiment (chiral discrimination by NMR spectroscopy)
-
Mattiza JT, Meyer V, Ozuduru G, Heine T, Fohrer J, Duddeck H (2012) Competition of ester, amide, ether, carbonate, alcohol and epoxide ligands in the dirhodium experiment (chiral discrimination by NMR spectroscopy). Nat Prod Commun 7: 359-362
-
(2012)
Nat Prod Commun
, vol.7
, pp. 359-362
-
-
Mattiza, J.T.1
Meyer, V.2
Ozuduru, G.3
Heine, T.4
Fohrer, J.5
Duddeck, H.6
-
198
-
-
61849113251
-
A new method proposed for the determination of absolute configurations of α-amino acids
-
Gomez ED, Duddeck H (2009) A new method proposed for the determination of absolute configurations of α-amino acids. Magn Reson Chem 47: 222-227
-
(2009)
Magn Reson Chem
, vol.47
, pp. 222-227
-
-
Gomez, E.D.1
Duddeck, H.2
-
199
-
-
71849094416
-
Studies on the configuration of nitrogenous stereogenic centres in adducts of rhodium(II) tetraacylates with chiral amines: The application of 1H and 13C NMR spectroscopy
-
Jazwinski J, Sadlej A (2009) Studies on the configuration of nitrogenous stereogenic centres in adducts of rhodium(II) tetraacylates with chiral amines: the application of 1H and 13C NMR spectroscopy. Tetrahedron Asymmetry 20: 2331-2343
-
(2009)
Tetrahedron Asymmetry
, vol.20
, pp. 2331-2343
-
-
Jazwinski, J.1
Sadlej, A.2
-
200
-
-
78149284459
-
Adducts of rhodium(II) tetraacylates with methionine and its derivatives: 1H and 13C nuclear magnetic resonance spectroscopy and chiral recognition
-
Glaszczka R, Jazwinski J, Kamienski B, Kaminska M (2010) Adducts of rhodium(II) tetraacylates with methionine and its derivatives: 1H and 13C nuclear magnetic resonance spectroscopy and chiral recognition. Tetrahedron Asymmetry 21: 2346-2355
-
(2010)
Tetrahedron Asymmetry
, vol.21
, pp. 2346-2355
-
-
Glaszczka, R.1
Jazwinski, J.2
Kamienski, B.3
Kaminska, M.4
-
201
-
-
70350541251
-
Comparing various chiral dirhodium tetracarboxylates in the dirhodium method
-
Mattiza JT, Harada N, Kuwahara S, Hassan Z, Duddeck H (2009) Comparing various chiral dirhodium tetracarboxylates in the dirhodium method. Chirality 21: 843-849
-
(2009)
Chirality
, vol.21
, pp. 843-849
-
-
Mattiza, J.T.1
Harada, N.2
Kuwahara, S.3
Hassan, Z.4
Duddeck, H.5
-
202
-
-
80052781048
-
Optimizing dirhodium(II) tetrakiscarboxylates as chiral NMR auxiliaries
-
Mattiza JT, Fohrer JGG, Duddeck H, GardinerMG, GhanemA (2011) Optimizing dirhodium(II) tetrakiscarboxylates as chiral NMR auxiliaries. Org Biomol Chem 9: 6542-6550
-
(2011)
Org Biomol Chem
, vol.9
, pp. 6542-6550
-
-
Mattiza, J.T.1
Fohrer, J.G.G.2
Duddeck, H.3
Gardiner, M.G.4
Ghanem, A.5
-
203
-
-
0031267871
-
Resolutions of tertiary phosphines and arsines with orthometallated palladium(II)-amine complexes
-
Wild SB (1997) Resolutions of tertiary phosphines and arsines with orthometallated palladium(II)-amine complexes. Coord Chem Rev 166: 291-311
-
(1997)
Coord Chem Rev
, vol.166
, pp. 291-311
-
-
Wild, S.B.1
-
204
-
-
0036313689
-
Overall view of the use of chiral platinum(II) complexes as chiral derivatizing agents (CDAs) for the enantiodiscrimination of unsaturated compounds by 195Pt NMR
-
Uccello-Barretta G, Bernardini R, Balzano F, Salvadori P (2002) Overall view of the use of chiral platinum(II) complexes as chiral derivatizing agents (CDAs) for the enantiodiscrimination of unsaturated compounds by 195Pt NMR. Chirality 14: 484-489
-
(2002)
Chirality
, vol.14
, pp. 484-489
-
-
Uccello-Barretta, G.1
Bernardini, R.2
Balzano, F.3
Salvadori, P.4
-
205
-
-
70349312934
-
Chiral orthopalladated and - Platinated arylphosphite complexes
-
Li J, Siegler MA, Lutz M, Spek AL, Gebbink RJMK, van Koten G (2009) Chiral orthopalladated and - platinated arylphosphite complexes. Organomet 28: 5323-5332
-
(2009)
Organomet
, vol.28
, pp. 5323-5332
-
-
Li, J.1
Siegler, M.A.2
Lutz, M.3
Spek, A.L.4
Gebbink, R.J.M.K.5
Van Koten, G.6
-
206
-
-
1642496745
-
Chiral recognition in silver(I) olefin complexes with chiral diamines. Resolution of racemic alkenes and NMR discrimination of enantiomers
-
Cucciolito ME, Flores G, Vitagliano A (2004) Chiral recognition in silver(I) olefin complexes with chiral diamines. Resolution of racemic alkenes and NMR discrimination of enantiomers. Organometallics 23: 15-17
-
(2004)
Organometallics
, vol.23
, pp. 15-17
-
-
Cucciolito, M.E.1
Flores, G.2
Vitagliano, A.3
-
207
-
-
33947496868
-
Selective NMR excitations in chiral analysis
-
Farjon J, Ziani L, Beguin L, Merlet D, Courtieu J (2007) Selective NMR excitations in chiral analysis. Annual Rep NMR Spectrosc 61: 283-293
-
(2007)
Annual Rep NMR Spectrosc
, vol.61
, pp. 283-293
-
-
Farjon, J.1
Ziani, L.2
Beguin, L.3
Merlet, D.4
Courtieu, J.5
-
208
-
-
67650098659
-
Analyses of proton NMR spectra of strongly and weakly dipolar coupled spins: Special emphasis on spectral simplification, chiral discrimination, and discerning of degenerate transitions
-
Baishya B, Prabhu UR, Suryaprakash N (2009) Analyses of proton NMR spectra of strongly and weakly dipolar coupled spins: special emphasis on spectral simplification, chiral discrimination, and discerning of degenerate transitions. Annual Rep NMR Spectrosc 67: 331-423
-
(2009)
Annual Rep NMR Spectrosc
, vol.67
, pp. 331-423
-
-
Baishya, B.1
Prabhu, U.R.2
Suryaprakash, N.3
-
209
-
-
79955713011
-
One and two dimensional single quantum and multiple quantum NMR methodologies: Tools for chiral analyses
-
Nath N, Hebbar S, Prabhu UR, Suryaprakash N (2010) One and two dimensional single quantum and multiple quantum NMR methodologies: tools for chiral analyses. J Indian Inst Sci 90: 1-36
-
(2010)
J Indian Inst Sci
, vol.90
, pp. 1-36
-
-
Nath, N.1
Hebbar, S.2
Prabhu, U.R.3
Suryaprakash, N.4
-
210
-
-
79955051333
-
SERF-filtered experiments: New enantio-selective tools for deciphering complex spectra of racemic mixtures dissolved in chiral oriented media
-
Farjon J, Merlet D (2011) SERF-filtered experiments: new enantio-selective tools for deciphering complex spectra of racemic mixtures dissolved in chiral oriented media. J Magn Reson 210: 24-30
-
(2011)
J Magn Reson
, vol.210
, pp. 24-30
-
-
Farjon, J.1
Merlet, D.2
-
211
-
-
79953217963
-
Spin-spin coupling edition in chiral liquid crystal NMR solvent
-
Merlet D, Beguin L, Courtieu J, Giraud N (2011) Spin-spin coupling edition in chiral liquid crystal NMR solvent. J Magn Reson 209: 315-322
-
(2011)
J Magn Reson
, vol.209
, pp. 315-322
-
-
Merlet, D.1
Beguin, L.2
Courtieu, J.3
Giraud, N.4
-
212
-
-
78651247931
-
Quantification of enantiomeric excess by 1H-detected heteronuclear refocusing and homonuclear multiple quantum NMR experiments
-
Nath N, Suryaprakash N (2011) Quantification of enantiomeric excess by 1H-detected heteronuclear refocusing and homonuclear multiple quantum NMR experiments. Chem Phys Lett 502: 136-143
-
(2011)
Chem Phys Lett
, vol.502
, pp. 136-143
-
-
Nath, N.1
Suryaprakash, N.2
-
213
-
-
67650253835
-
Natural abundance deuterium NMR spectroscopy: Developments and analytical applications in liquids, liquid crystals and solid phases
-
Lesot P, Courtieu J (2009) Natural abundance deuterium NMR spectroscopy: developments and analytical applications in liquids, liquid crystals and solid phases. Prog NMR Spectrosc 55: 128-159
-
(2009)
Prog NMR Spectrosc
, vol.55
, pp. 128-159
-
-
Lesot, P.1
Courtieu, J.2
-
214
-
-
44649138566
-
Enantiomeric analysis using natural abundance deuterium 3D NMR spectroscopy in polypeptide chiral oriented media
-
Lesot P, Lafon O (2008) Enantiomeric analysis using natural abundance deuterium 3D NMR spectroscopy in polypeptide chiral oriented media. Chem Phys Lett 458: 219-222
-
(2008)
Chem Phys Lett
, vol.458
, pp. 219-222
-
-
Lesot, P.1
Lafon, O.2
-
215
-
-
79957961858
-
Fast and high-resolution stereochemical analysis by nonuniform sampling and covariance processing of anisotropic natural abundance 2D 2H NMR datasets
-
Lafon O, Hu B, Amoureux JP, Lesot P (2011) Fast and high-resolution stereochemical analysis by nonuniform sampling and covariance processing of anisotropic natural abundance 2D 2H NMR datasets. Chem Eur J 17: 6716-6724
-
(2011)
Chem Eur J
, vol.17
, pp. 6716-6724
-
-
Lafon, O.1
Hu, B.2
Amoureux, J.P.3
Lesot, P.4
-
216
-
-
34447573944
-
Homo- and heteronuclear 2D NMR approaches to analyse a mixture of deuterated unlike/like stereoisomers using weakly ordering chiral liquid crystals
-
Ali KB, Lafon O, Zimmermann H, Guittet E, Lesot P (2007) Homo- and heteronuclear 2D NMR approaches to analyse a mixture of deuterated unlike/like stereoisomers using weakly ordering chiral liquid crystals. J Magn Reson 187: 205-215
-
(2007)
J Magn Reson
, vol.187
, pp. 205-215
-
-
Ali, K.B.1
Lafon, O.2
Zimmermann, H.3
Guittet, E.4
Lesot, P.5
-
217
-
-
44649139296
-
2H NMR studies on two-homopolypeptide lyotropic enantiodiscriminating mesophases: Experimental quantification of solute-fiber affinities
-
Lesot P, Lafon O, Aroulanda C, Dong RY (2008) 2H NMR studies on two-homopolypeptide lyotropic enantiodiscriminating mesophases: experimental quantification of solute-fiber affinities. Chem Eur J 14: 4082-4092
-
(2008)
Chem Eur J
, vol.14
, pp. 4082-4092
-
-
Lesot, P.1
Lafon, O.2
Aroulanda, C.3
Dong, R.Y.4
-
218
-
-
70849123539
-
NMR (pro)chiral discrimination using polysaccharide gels
-
Naumann C, Kuchel PW (2009) NMR (pro)chiral discrimination using polysaccharide gels. Chem Eur J 15: 12189-12191
-
(2009)
Chem Eur J
, vol.15
, pp. 12189-12191
-
-
Naumann, C.1
Kuchel, P.W.2
-
219
-
-
70849110508
-
Covalently cross-linked gelatin allows chiral differentiation at elevated temperatures and in DMSO
-
Kummerlowe G, Kiran MU, Luy B (2009) Covalently cross-linked gelatin allows chiral differentiation at elevated temperatures and in DMSO. Chem Eur J 15: 12192-12195
-
(2009)
Chem Eur J
, vol.15
, pp. 12192-12195
-
-
Kummerlowe, G.1
Kiran, M.U.2
Luy, B.3
-
220
-
-
79953710566
-
Naturally occurring biodegradable polymers as the basis of chiral gels for the differentiation of enantiomers by partially oriented NMR spectroscopy
-
Buchler SSD, Kummerlowe G, Luy B (2011) Naturally occurring biodegradable polymers as the basis of chiral gels for the differentiation of enantiomers by partially oriented NMR spectroscopy. Int J Artif Organs 34: 134-138
-
(2011)
Int J Artif Organs
, vol.34
, pp. 134-138
-
-
Buchler, S.S.D.1
Kummerlowe, G.2
Luy, B.3
-
221
-
-
61949419129
-
Visualization of enantiomers in liquid-crystalline phase of a fragmented DNA solution
-
Sau SP, Ramanathan KV (2009) Visualization of enantiomers in liquid-crystalline phase of a fragmented DNA solution. J Phys Chem B 113: 1530-1532
-
(2009)
J Phys Chem B
, vol.113
, pp. 1530-1532
-
-
Sau, S.P.1
Ramanathan, K.V.2
-
222
-
-
80054726315
-
Exploring the spectral enantiodiscrimination potential of a DNA-based orienting medium using deuterium NMR spectroscopy
-
Lesot P, Reddy UV, Suryaprakash N (2011) Exploring the spectral enantiodiscrimination potential of a DNA-based orienting medium using deuterium NMR spectroscopy. Chem Commun 47: 11736-11738
-
(2011)
Chem Commun
, vol.47
, pp. 11736-11738
-
-
Lesot, P.1
Reddy, U.V.2
Suryaprakash, N.3
-
223
-
-
42349108638
-
Combined analysis of C-18 unsaturated fatty acids using natural abundance deuterium 2D NMR spectroscopy in chiral oriented solvents
-
Lesot P, Baillif V, Billault I (2008) Combined analysis of C-18 unsaturated fatty acids using natural abundance deuterium 2D NMR spectroscopy in chiral oriented solvents. Anal Chem 80: 2963-2972
-
(2008)
Anal Chem
, vol.80
, pp. 2963-2972
-
-
Lesot, P.1
Baillif, V.2
Billault, I.3
-
224
-
-
79251639035
-
Recent advances in the analysis of the site-specific isotopic fractionation of metabolites such as fatty acids using anisotropic natural-abundance 2H NMR spectroscopy: Application to conjugated linolenic methyl esters
-
Lesot P, Serhan Z, Billault I (2011) Recent advances in the analysis of the site-specific isotopic fractionation of metabolites such as fatty acids using anisotropic natural-abundance 2H NMR spectroscopy: application to conjugated linolenic methyl esters. Anal Bioanal Chem 399: 1187-1200
-
(2011)
Anal Bioanal Chem
, vol.399
, pp. 1187-1200
-
-
Lesot, P.1
Serhan, Z.2
Billault, I.3
-
225
-
-
84858705428
-
Probing substrateproduct relationships by natural abundance deuterium 2D NMR spectroscopy in liquidcrystalline solvents: Epoxidation of linoleate to vernoleate by two different plant enzymes
-
Billault I, Le Du A, Ouethrani M, Serhan Z, Lesot P, Robins RJ (2012) Probing substrateproduct relationships by natural abundance deuterium 2D NMR spectroscopy in liquidcrystalline solvents: epoxidation of linoleate to vernoleate by two different plant enzymes. Anal Bioanal Chem 402: 2985-2998
-
(2012)
Anal Bioanal Chem
, vol.402
, pp. 2985-2998
-
-
Billault, I.1
Le Du, A.2
Ouethrani, M.3
Serhan, Z.4
Lesot, P.5
Robins, R.J.6
-
226
-
-
34547308880
-
NMR in chiral polypeptide liquid crystals: The problem of amines
-
Solgadi A, Jean L, Lasne MC, Rouden J, Courtieu J, Meddour A (2007) NMR in chiral polypeptide liquid crystals: the problem of amines. Tetrahedron Asymmetry 18: 1511-1516
-
(2007)
Tetrahedron Asymmetry
, vol.18
, pp. 1511-1516
-
-
Solgadi, A.1
Jean, L.2
Lasne, M.C.3
Rouden, J.4
Courtieu, J.5
Meddour, A.6
-
227
-
-
34548200680
-
Chiral discrimination in the 13C and 2H NMR of the crown and saddle isomers of nonamethoxy-cyclotriveratrylene in chiral liquid-crystalline solutions
-
Lafon O, Lesot P, Zimmermann H, Poupko R, Luz Z (2007) Chiral discrimination in the 13C and 2H NMR of the crown and saddle isomers of nonamethoxy-cyclotriveratrylene in chiral liquid-crystalline solutions. J Phys Chem B 111: 9453-9467
-
(2007)
J Phys Chem B
, vol.111
, pp. 9453-9467
-
-
Lafon, O.1
Lesot, P.2
Zimmermann, H.3
Poupko, R.4
Luz, Z.5
-
228
-
-
46949088455
-
Enantiodiscrimination in deuterium NMR spectra of flexible chiral molecules with average axial symmetry dissolved in chiral liquid crystals: The case of tridioxyethylenetriphenylene
-
Lesot P, Lafon O, Zimmermann H, Luz Z (2008) Enantiodiscrimination in deuterium NMR spectra of flexible chiral molecules with average axial symmetry dissolved in chiral liquid crystals: the case of tridioxyethylenetriphenylene. J Am Chem Soc 130: 8754-8761
-
(2008)
J Am Chem Soc
, vol.130
, pp. 8754-8761
-
-
Lesot, P.1
Lafon, O.2
Zimmermann, H.3
Luz, Z.4
-
229
-
-
68149092140
-
Enantiodiscrimination in flexible cyclic solutes using NMR spectroscopy in polypeptide chiral mesophases: Investigation of cis-decalin and THF
-
Aroulanda C, Lafon O, Lesot P (2009) Enantiodiscrimination in flexible cyclic solutes using NMR spectroscopy in polypeptide chiral mesophases: investigation of cis-decalin and THF. J Phys Chem B 113: 10628-10640
-
(2009)
J Phys Chem B
, vol.113
, pp. 10628-10640
-
-
Aroulanda, C.1
Lafon, O.2
Lesot, P.3
-
230
-
-
34250335976
-
Analysis of intramolecular dynamic processes in enantiomeric diaryl atropisomers and related derivatives by 2H NMR spectroscopy in polypeptide liquid crystals
-
Lafon O, Lesot P, Fan CA, Kagan HB (2007) Analysis of intramolecular dynamic processes in enantiomeric diaryl atropisomers and related derivatives by 2H NMR spectroscopy in polypeptide liquid crystals. Chem Eur J 13: 3772-3786
-
(2007)
Chem Eur J
, vol.13
, pp. 3772-3786
-
-
Lafon, O.1
Lesot, P.2
Fan, C.A.3
Kagan, H.B.4
-
231
-
-
58749094951
-
Two aspects of the desymmetrization of selected prochiral aromatic or vinylic dihalides: Enantioselective halogen-lithium exchange and prochiral recognition in chiral liquid crystals
-
Fan CA, Ferber B, Kagan HB, Lafon O, Lesot P (2008) Two aspects of the desymmetrization of selected prochiral aromatic or vinylic dihalides: enantioselective halogen-lithium exchange and prochiral recognition in chiral liquid crystals. Tetrahedron Asymmetry 19: 2666-2677
-
(2008)
Tetrahedron Asymmetry
, vol.19
, pp. 2666-2677
-
-
Fan, C.A.1
Ferber, B.2
Kagan, H.B.3
Lafon, O.4
Lesot, P.5
-
232
-
-
77956404657
-
Cationic planar chiral (η6-arene)Mn(CO)3 + complexes: Resolution, NMR study in chiral-oriented solvents, and applications to the enantioselective synthesis of 4-substituted cyclohexenones and (η6-phosphinoarene)Mn(CO)3 + complexes
-
Eloi A, Rose-Munch F, Rose E, Pille A, Lesot P, Herson P (2010) Cationic planar chiral (η6-arene)Mn(CO)3 + complexes: resolution, NMR study in chiral-oriented solvents, and applications to the enantioselective synthesis of 4-substituted cyclohexenones and (η6-phosphinoarene)Mn(CO)3 + complexes. Organomet 29: 3876-3886
-
(2010)
Organomet
, vol.29
, pp. 3876-3886
-
-
Eloi, A.1
Rose-Munch, F.2
Rose, E.3
Pille, A.4
Lesot, P.5
Herson, P.6
-
233
-
-
79954558642
-
Enantiotopic discrimination in the deuterium NMR spectrum of solutes with S4 symmetry in chiral liquid crystals
-
Aroulanda C, Zimmermann H, Luz Z, Lesot P (2011) Enantiotopic discrimination in the deuterium NMR spectrum of solutes with S4 symmetry in chiral liquid crystals. J Chem Phys 134: 134502-134508
-
(2011)
J Chem Phys
, vol.134
, pp. 134502-134508
-
-
Aroulanda, C.1
Zimmermann, H.2
Luz, Z.3
Lesot, P.4
-
234
-
-
36148981416
-
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 (2007) Empirical determination of the absolute configuration of small chiral molecules using natural abundance 2H NMR in chiral liquid crystals. Chem Commun 43: 4737-4739
-
(2007)
Chem Commun
, vol.43
, pp. 4737-4739
-
-
Ziani, L.1
Lesot, P.2
Meddour, A.3
Courtieu, J.4
-
235
-
-
0042689812
-
Probing the diastereotopicity of methylene protons in strychnine using residual dipolar couplings
-
Thiele CM, Berger S (2003) Probing the diastereotopicity of methylene protons in strychnine using residual dipolar couplings. Org Lett 5: 705-708
-
(2003)
Org Lett
, vol.5
, pp. 705-708
-
-
Thiele, C.M.1
Berger, S.2
-
236
-
-
6344229751
-
Simultaneous assignment of all diastereotopic protons in strychnine using RDCs: PELG as alignment medium for organic molecules
-
Thiele CM (2004) Simultaneous assignment of all diastereotopic protons in strychnine using RDCs: PELG as alignment medium for organic molecules. J Org Chem 69: 7403-7413
-
(2004)
J Org Chem
, vol.69
, pp. 7403-7413
-
-
Thiele, C.M.1
-
237
-
-
38849137928
-
Stretched poly(methyl methacrylate) gel aligns small organic molecules in chloroform. Stereochemical analysis and diastereotopic proton NMR assignment in ludartin using residual dipolar couplings and 3J coupling constant analysis
-
Gil RR, Gayathri C, Tsarevsky NV, Matyjaszewski K (2008) Stretched poly(methyl methacrylate) gel aligns small organic molecules in chloroform. Stereochemical analysis and diastereotopic proton NMR assignment in ludartin using residual dipolar couplings and 3J coupling constant analysis. J Org Chem 73: 840-848
-
(2008)
J Org Chem
, vol.73
, pp. 840-848
-
-
Gil, R.R.1
Gayathri, C.2
Tsarevsky, N.V.3
Matyjaszewski, K.4
-
238
-
-
75749147990
-
Enhancing the orienting properties of poly(γ-benzyl- L-glutamate) by means of additives
-
Marx A, Bottcher B, Thiele CM (2010) Enhancing the orienting properties of poly(γ-benzyl- L-glutamate) by means of additives. Chem Eur J 16: 1656-1663
-
(2010)
Chem Eur J
, vol.16
, pp. 1656-1663
-
-
Marx, A.1
Bottcher, B.2
Thiele, C.M.3
-
239
-
-
41949136093
-
RDCenhanced NMR spectroscopy in structure elucidation of sucro-neolambertellin
-
Schuetz A, Murakami T, Takada N, Junker J, Hashimoto M, Griesinger C (2008) RDCenhanced NMR spectroscopy in structure elucidation of sucro-neolambertellin. Angew Chem Int Ed 47: 2032-2034
-
(2008)
Angew Chem Int Ed
, vol.47
, pp. 2032-2034
-
-
Schuetz, A.1
Murakami, T.2
Takada, N.3
Junker, J.4
Hashimoto, M.5
Griesinger, C.6
-
240
-
-
79551491339
-
Bijvoet in solution reveals unexpected stereoselectivity in a Michael addition
-
Sun H, d'Auvergne EJ, Reinscheid UM, Dias LC, Andrade CKZ, Rocha RO, Griesinger C (2011) Bijvoet in solution reveals unexpected stereoselectivity in a Michael addition. Chem Eur J 17: 1811-1817
-
(2011)
Chem Eur J
, vol.17
, pp. 1811-1817
-
-
Sun, H.1
D'Auvergne, E.J.2
Reinscheid, U.M.3
Dias, L.C.4
Andrade, C.K.Z.5
Rocha, R.O.6
Griesinger, C.7
-
241
-
-
84864692376
-
Determination of the absolute configuration of 19-OH-(-)-eburnamonine using a combination of residual dipolar couplings, DFT chemical shift predications and chiroptics
-
Trigo-Mourino P, Sifuentes R, Navarro-Vazquez A, Gayathri C, Maruenda H, Gil RR (2012) Determination of the absolute configuration of 19-OH-(-)-eburnamonine using a combination of residual dipolar couplings, DFT chemical shift predications and chiroptics. Nat Prod Commun 7: 735-738
-
(2012)
Nat Prod Commun
, vol.7
, pp. 735-738
-
-
Trigo-Mourino, P.1
Sifuentes, R.2
Navarro-Vazquez, A.3
Gayathri, C.4
Maruenda, H.5
Gil, R.R.6
-
242
-
-
34748914846
-
Stereochemical identification of (R)- and (S)-ibuprofen using residual dipolar couplings, NMR, and modeling
-
Marathias VM, Tawa GJ, Goijer I, Bach AC (2007) Stereochemical identification of (R)- and (S)-ibuprofen using residual dipolar couplings, NMR, and modeling. Chirality 19: 741-750
-
(2007)
Chirality
, vol.19
, pp. 741-750
-
-
Marathias, V.M.1
Tawa, G.J.2
Goijer, I.3
Bach, A.C.4
-
243
-
-
79957598208
-
Spin-selective correlation experiment for measurement of long-range J couplings and for assignment of (R/S) enantiomers from residual dipolar couplings and DFT
-
Nath N, Suryaprakash N (2011) Spin-selective correlation experiment for measurement of long-range J couplings and for assignment of (R/S) enantiomers from residual dipolar couplings and DFT. J Phys Chem B 115: 6868-6875
-
(2011)
J Phys Chem B
, vol.115
, pp. 6868-6875
-
-
Nath, N.1
Suryaprakash, N.2
-
244
-
-
84864884012
-
Is enantiomer assignment possible in NMR spectroscopy using residual dipolar couplings from chiral nonracemic alignment media? - A critical assessment
-
Berger R, Courtieu J, Gil RR, Griesinger C, Kock M, Lesot P, Luy B, Merlet D, Navarro- Vazquez A, Reggelin M, Reinscheid UM, Thiele C, Zweckstetter M (2012) Is enantiomer assignment possible in NMR spectroscopy using residual dipolar couplings from chiral nonracemic alignment media? - A critical assessment. Angew Chem Int Ed 51: 8388-8391
-
(2012)
Angew Chem Int Ed
, vol.51
, pp. 8388-8391
-
-
Berger, R.1
Courtieu, J.2
Gil, R.R.3
Griesinger, C.4
Kock, M.5
Lesot, P.6
Luy, B.7
Merlet, D.8
Navarro-Vazquez, A.9
Reggelin, M.10
Reinscheid, U.M.11
Thiele, C.12
Zweckstetter, M.13
-
245
-
-
77954263494
-
Evolution of the Saupe order parameters of enantiomers from a racemic to a non-racemic liquid crystal solvent: An original light on the absolute configuration determination problem
-
Courtieu J, Aroulanda C, Lesot P, Meddour A, Merlet D (2010) Evolution of the Saupe order parameters of enantiomers from a racemic to a non-racemic liquid crystal solvent: an original light on the absolute configuration determination problem. Liq Cryst 37: 903-912
-
(2010)
Liq Cryst
, vol.37
, pp. 903-912
-
-
Courtieu, J.1
Aroulanda, C.2
Lesot, P.3
Meddour, A.4
Merlet, D.5
-
246
-
-
77951813400
-
Residual dipolar couplings for the configurational and conformational analysis of organic molecules
-
Kummerlowe G, Luy B (2009) Residual dipolar couplings for the configurational and conformational analysis of organic molecules. Annu Rep NMR Spectrosc 68: 193-230
-
(2009)
Annu Rep NMR Spectrosc
, vol.68
, pp. 193-230
-
-
Kummerlowe, G.1
Luy, B.2
-
247
-
-
78649820881
-
Differentiation of enantiomers by NMR spectroscopy using chiral orienting media
-
Luy B (2010) Differentiation of enantiomers by NMR spectroscopy using chiral orienting media. J Indian Inst Sci 90: 119-132
-
(2010)
J Indian Inst Sci
, vol.90
, pp. 119-132
-
-
Luy, B.1
|