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Volumn 23, Issue 3, 2011, Pages 222-227

Structural influence of chiral tertiary aminonaphthol ligands on the asymmetric phenyl transfer to aromatic aldehydes

Author keywords

aminonaphthol; asymmetric phenyl transfer; electronic and steric effects

Indexed keywords

1 [ PHENYL[METHYL[ 1' PHENYLETHYL] AMINO]METHYL] 2 NAPHTHOL; 1 [(2 CHLOROPHENYL)[METHYL[ 1' PHENYLETHYL]AMINO]METHYL] 2 NAPHTHOL; 1 [(2 FURYLPHENYL)[METHYL[ 1' PHENYLETHYL]AMINO]METHYL] 2 NAPHTHOL; 1 [(2 METHYLPHENYL)[METHYL[ 1' PHENYLETHYL]AMINO]METHYL] 2 NAPHTHOL; 1 [(3 FURYLPHENYL)[METHYL[ 1' PHENYLETHYL]AMINO]METHYL] 2 NAPHTHOL; 1 [(3 METHOXYPHENYL)[METHYL[ 1' PHENYLETHYL]AMINO]METHYL] 2 NAPHTHOL; 1 [(3 METHYLPHENYL)[METHYL[ 1' PHENYLETHYL]AMINO]METHYL] 2 NAPHTHOL; 1 [(3,5 DIMETHYLPHENYL)[METHYL[ 1' PHENYLETHYL]AMINO]METHYL] 2 NAPHTHOL; 1 [(4 CHLOROPHENYL)[METHYL[ 1' PHENYLETHYL]AMINO]METHYL] 2 NAPHTHOL; 1 [(4 FURYLPHENYL)[METHYL[ 1' PHENYLETHYL]AMINO]METHYL] 2 NAPHTHOL; 1 [(4 METHOXYPHENYL)[METHYL[ 1' PHENYLETHYL]AMINO]METHYL] 2 NAPHTHOL; 1 [(4 METHYLPHENYL)[METHYL[ 1' PHENYLETHYL]AMINO]METHYL] 2 NAPHTHOL; 1 NAPHTHOL DERIVATIVE; 2 NAPHTHOL; ALDEHYDE; ALDEHYDE DERIVATIVE; ALPHA METHYLBENZYLAMINE; LIGAND; PHENYL GROUP; TERTIARY AMINONAPHTHOL LIGAND DERIVATIVE; UNCLASSIFIED DRUG;

EID: 79951479863     PISSN: 08990042     EISSN: 1520636X     Source Type: Journal    
DOI: 10.1002/chir.20903     Document Type: Article
Times cited : (24)

References (49)
  • 1
    • 0015116399 scopus 로고
    • Stereochemical aspects of antihistamine action. 4. Absolute configuration of carbinoxamine antipodes
    • Barouh V, Dall H, Patel D, Hite G,. Stereochemical aspects of antihistamine action. 4. Absolute configuration of carbinoxamine antipodes. J Med Chem 1971; 14: 834-836.
    • (1971) J Med Chem , vol.14 , pp. 834-836
    • Barouh, V.1    Dall, H.2    Patel, D.3    Hite, G.4
  • 2
    • 0022360341 scopus 로고
    • New 1,4-dihydropyridine derivatives with potent and long-lasting hypotensive effect
    • Meguro K, Aizawa M, Sohda T, Kawamatsu Y, Nagaoka A,. New 1,4-dihydropyridine derivatives with potent and long-lasting hypotensive effect. Chem Pharm Bull 1985; 33: 3787-3797. (Pubitemid 16235704)
    • (1985) Chemical and Pharmaceutical Bulletin , vol.33 , Issue.9 , pp. 3787-3797
    • Meguro, K.1    Aizawa, M.2    Sohda, T.3
  • 3
    • 0000945168 scopus 로고
    • A new preparative method for optically active diarylcarbinols
    • Toda F, Tanaka K, Koshiro K,. A new preparative method for optically active diarylcarbinols. Tetrahedron Asymmetry 1991; 2: 873-874.
    • (1991) Tetrahedron Asymmetry , vol.2 , pp. 873-874
    • Toda, F.1    Tanaka, K.2    Koshiro, K.3
  • 4
    • 0026782201 scopus 로고
    • Stereochemical studies of chiral H-1 antagonists of histamine: The resolution, chiral analysis, and biological evaluation of four antipodal pairs
    • Casy AF, Drake AF, Ganellin CR, Mercer AD, Upton C,. Stereochemical studies of chiral H-1 antagonists of histamine: the resolution, chiral analysis, and biological evaluation of four antipodal pairs. Chirality 1992; 4: 356-366.
    • (1992) Chirality , vol.4 , pp. 356-366
    • Casy, A.F.1    Drake, A.F.2    Ganellin, C.R.3    Mercer, A.D.4    Upton, C.5
  • 5
    • 0028855517 scopus 로고
    • Synthesis, absolute configuration and circular dichroism of some diarylmethane derivatives
    • Stanchev S, Rakovska R, Berova N, Snatzke G,. Synthesis, absolute configuration and circular dichroism of some diarylmethane derivatives. Tetrahedron Asymmetry 1995; 6: 183-198.
    • (1995) Tetrahedron Asymmetry , vol.6 , pp. 183-198
    • Stanchev, S.1    Rakovska, R.2    Berova, N.3    Snatzke, G.4
  • 6
    • 0030570857 scopus 로고    scopus 로고
    • Asymmetric synthesis of (S)-carbinoxamine. New aspects of oxazaborolidine-catalyzed enantioselective carbonyl reduction
    • DOI 10.1016/0040-4039(96)01198-7
    • Corey EJ, Helal CJ,. Asymmetric synthesis of (S)-carbinoxamine. New aspects of oxazaborolidine-catalyzed enantioselective carbony1 reduction. Tetrahedron Lett 1996; 37: 5675-5678. (Pubitemid 26245953)
    • (1996) Tetrahedron Letters , vol.37 , Issue.32 , pp. 5675-5678
    • Corey, E.J.1    Helal, C.J.2
  • 7
    • 0029952317 scopus 로고    scopus 로고
    • Synthesis of aryl 2-benzofuranyl and aryl 2-indolyl carbinols of high enantiomeric purity via palladium-catalyzed heteroannulation of chiral arylpropargylic alcohols
    • DOI 10.1016/0957-4166(96)00138-3
    • Botta M, Summa V, Corelli F, DiPietro G, Lombardi P,. Synthesis of aryl 2-benzofuranyl and aryl 2-indolyl carbinols of high enantiomeric purity via palladium-catalyzed heteroannulation of chiral arylpropargylic alcohols. Tetrahedron Asymmetry 1996; 7: 1263-1266. (Pubitemid 26169961)
    • (1996) Tetrahedron Asymmetry , vol.7 , Issue.5 , pp. 1263-1266
    • Botta, M.1    Summa, V.2    Corelli, F.3    Di Pietro, G.4    Lombardi, P.5
  • 9
    • 22044432631 scopus 로고    scopus 로고
    • Catalyzed asymmetric aryl transfer reactions to aldehydes with boroxines as aryl source
    • DOI 10.1016/j.tetasy.2005.06.010, PII S0957416605004544
    • Wu XY, Liu XY, Zhao G,. Catalyzed asymmetric aryl transfer reactions to aldehydes with boroxines as aryl source. TetrahedronAsymmetry 2005; 16: 2299-2305. (Pubitemid 40967886)
    • (2005) Tetrahedron Asymmetry , vol.16 , Issue.13 , pp. 2299-2305
    • Wu, X.1    Liu, X.2    Zhao, G.3
  • 10
    • 24144492691 scopus 로고    scopus 로고
    • Highly effective and recyclable dendritic ligands for the enantioselective aryl transfer reactions to aldehydes
    • DOI 10.1021/jo050994h
    • Liu XY, Wu XY, Chai Z, Wu YY, Zhao G, Zhu SZ,. Highly effective and recyclable dendritic ligands for the enantioselective aryl transfer reactions to aldehydes. J Org Chem 2005; 70: 7432-7435. (Pubitemid 41233288)
    • (2005) Journal of Organic Chemistry , vol.70 , Issue.18 , pp. 7432-7435
    • Liu, X.Y.1    Wu, X.Y.2    Chai, Z.3    Wu, Y.Y.4    Zhao, G.5    Zhu, S.Z.6
  • 11
    • 20044366180 scopus 로고    scopus 로고
    • Catalytic enantioselective arylation of aldehydes: Boronic acids as a suitable source of transferable aryl groups
    • DOI 10.1039/b501485a
    • Braga AL, Ludtke DS, Vargas F, Paixo MW,. Catalytic enantioselective arylation of aldehydes: boronic acids as a suitable source of transferable aryl groups. Chem Commun 2005; 19: 2512-2514. (Pubitemid 40769167)
    • (2005) Chemical Communications , Issue.19 , pp. 2512-2514
    • Braga, A.L.1    Ludtke, D.S.2    Vargas, F.3    Paixao, M.W.4
  • 12
    • 33749120749 scopus 로고    scopus 로고
    • The synthesis of N,O-ferrocenyl pyrrolidine-containing ligands and their application in the diethyl- and diphenylzinc addition to aromatic aldehydes
    • DOI 10.1021/jo060894r
    • Ahern T, Bunz HM, Guiry PJ,. The synthesis of N,O-ferrocenyl pyrrolidine-containing ligands and their application in the diethyl- and diphenylzinc addition to aromatic aldehydes. J Org Chem 2006; 71: 7596-7602. (Pubitemid 44470298)
    • (2006) Journal of Organic Chemistry , vol.71 , Issue.20 , pp. 7596-7602
    • Ahern, T.1    Muller-Bunz, H.2    Guiry, P.J.3
  • 13
    • 30744438853 scopus 로고    scopus 로고
    • Asymmetric synthesis of functionalized diarylmethanols catalyzed by a new γ-amino thiol
    • Wu PY, Wu HL, Uang BJ,. Asymmetric synthesis of functionalized diarylmethanols catalyzed by a new γ-amino thiol. J Org Chem 2006; 71: 833-835.
    • (2006) J Org Chem , vol.71 , pp. 833-835
    • Wu, P.Y.1    Wu, H.L.2    Uang, B.J.3
  • 14
    • 38349111414 scopus 로고    scopus 로고
    • Catalytic asymmetric alkynylation and arylation of aldehydes by an H8-binaphthyl-based amino alcohol ligand
    • Ruan JW, Lu G, Xu LJ, Chan ASC,. Catalytic asymmetric alkynylation and arylation of aldehydes by an H8-binaphthyl-based amino alcohol ligand. Adv Synth Catal 2008; 350: 76-84.
    • (2008) Adv Synth Catal , vol.350 , pp. 76-84
    • Ruan, J.W.1    Lu, G.2    Xu, L.J.3    Chan, A.S.C.4
  • 15
    • 38749124698 scopus 로고    scopus 로고
    • Catalytic asymmetric aryl transfer: Highly enantioselective preparation of (R)- and (S)-diarylmethanols catalyzed by the same chiral ferrocenyl aziridino alcohol
    • Wang MC, Wang XD, Ding X, Liu ZK,. Catalytic asymmetric aryl transfer: highly enantioselective preparation of (R)- and (S)-diarylmethanols catalyzed by the same chiral ferrocenyl aziridino alcohol. Tetrahedron 2008; 64: 2559-2564.
    • (2008) Tetrahedron , vol.64 , pp. 2559-2564
    • Wang, M.C.1    Wang, X.D.2    Ding, X.3    Liu, Z.K.4
  • 16
    • 41749099717 scopus 로고    scopus 로고
    • Acceleration of arylzinc formation and its enantioselective addition to aldehydes by microwave irradiation and aziridine-2-methanol catalysts
    • DOI 10.1021/jo702413n
    • Braga AL, Paixao MW, Westermann B, Schneider PH, Wessjohann LA,. Acceleration of arylzinc formation and its enantioselective addition to aldehydes by microwave irradiation and aziridine-2-methanol catalysts. J Org Chem 2008; 73: 2879-2882. (Pubitemid 351485629)
    • (2008) Journal of Organic Chemistry , vol.73 , Issue.7 , pp. 2879-2882
    • Braga, A.L.1    Paixao, M.W.2    Westermann, B.3    Schneider, P.H.4    Wessjohann, L.A.5
  • 17
    • 46749134780 scopus 로고    scopus 로고
    • Highly enantioselective aryl transfer to aldehydes: A remarkable effect of sulfur substitution in amino thioacetate ligands
    • Jin MJ, Sarkar SM, Lee DH,;, Qiu H,. Highly enantioselective aryl transfer to aldehydes: a remarkable effect of sulfur substitution in amino thioacetate ligands. Org Lett 2008; 10: 1235-1237.
    • (2008) Org Lett , vol.10 , pp. 1235-1237
    • Jin, M.J.1    Sarkar, S.M.2    Lee, D.H.3    Qiu, H.4
  • 18
    • 63249114895 scopus 로고    scopus 로고
    • Catalytic enantioselective arylation of aryl aldehydes by chiral aminophenol ligands
    • Yang XF, Hirose T, Zhang GY,. Catalytic enantioselective arylation of aryl aldehydes by chiral aminophenol ligands. Tetrahedron Asymmetry 2009; 20: 415-419.
    • (2009) Tetrahedron Asymmetry , vol.20 , pp. 415-419
    • Yang, X.F.1    Hirose, T.2    Zhang, G.Y.3
  • 19
    • 75949121862 scopus 로고    scopus 로고
    • Continuous flow enantioselective arylation of aldehydes with ArZnEt using triarylboroxins as the ultimate source of aryl groups
    • Rolland J, Cambeiro XC, Escrich CR, Pericàs MA,. Continuous flow enantioselective arylation of aldehydes with ArZnEt using triarylboroxins as the ultimate source of aryl groups. Beilstenin J Org Chem 2009; 5: 56.
    • (2009) Beilstenin J Org Chem , vol.5 , pp. 56
    • Rolland, J.1    Cambeiro, X.C.2    Escrich, C.R.3    Pericàs, M.A.4
  • 20
    • 0001111641 scopus 로고    scopus 로고
    • Planar-Chiral Heterocycles as Ligands in Metal-Catalyzed Processes: Enantioselective Addition of Organozinc Reagents to Aldehydes
    • Dosa PI, Ruble JC, Fu GC,. Planar-chiral heterocycles as ligands in metal-catalyzed processes: enantioselective addition of organozinc reagents to aldehydes. J Org Chem 1997; 62: 444-445. (Pubitemid 127493264)
    • (1997) Journal of Organic Chemistry , vol.62 , Issue.3 , pp. 444-445
    • Dosa, P.I.1    Ruble, J.C.2    Fu, G.C.3
  • 21
    • 0039938946 scopus 로고    scopus 로고
    • Catalytic enantioselective aryl transfer: Asymmetric addition of diphenylzine to aldehydes
    • Bolm C, Muñiz K,. Catalytic enantioselective aryl transfer: asymmetric addition of diphenylzinc to aldehydes. Chem Commun 1999; 14: 1295-1296. (Pubitemid 29355453)
    • (1999) Chemical Communications , Issue.14 , pp. 1295-1296
    • Bolm, C.1    Muniz, K.2
  • 23
    • 0034596803 scopus 로고    scopus 로고
    • Asymmetric, catalytic phenyl transfer to aldehydes: Enantioselective synthesis of diarylmethanols
    • Bolm C, Hermanns N, Hildebrand JP, Muñiz K,. Asymmetric, catalytic phenyl transfer to aldehydes: enantioselective synthesis of diarylmethanols. Angew Chem Int Ed 2000; 39: 3465-3467.
    • (2000) Angew Chem Int Ed , vol.39 , pp. 3465-3467
    • Bolm, C.1    Hermanns, N.2    Hildebrand, J.P.3    Muñiz, K.4
  • 24
    • 0035101558 scopus 로고    scopus 로고
    • A novel ferrocenyl diselenide for the catalytic asymmetric aryl transfer to aldehydes
    • DOI 10.1039/b003237i
    • Bolm C, Kesselgruber M, Grenz A, Hermanns N, Hildebrand JP,. A novel ferrocenyl diselenide for the catalytic asymmetric aryl transfer to aldehydes. New J Chem 2001; 25: 13-15. (Pubitemid 32164792)
    • (2001) New Journal of Chemistry , vol.25 , Issue.1 , pp. 13-15
    • Bolm, C.1    Kesselgruber, M.2    Grenz, A.3    Hermanns, N.4    Hildebrand, J.P.5
  • 25
    • 0037132590 scopus 로고    scopus 로고
    • Catalyzed asymmetric aryl transfer reactions to aldehydes with boronic acids as aryl source
    • Bolm C, Rudolph J,. Catalyzed asymmetric aryl transfer reactions to aldehydes with boronic acids as aryl source. J Am Chem Soc 2002; 124: 14850-14581.
    • (2002) J Am Chem Soc , vol.124 , pp. 14850-14581
    • Bolm, C.1    Rudolph, J.2
  • 26
    • 2442636490 scopus 로고    scopus 로고
    • The MPEG effect: Improving asymmetric processes by simple additives
    • Rudolph J, Hermanns N, Bolm C,. The MPEG effect: improving asymmetric processes by simple additives. J Org Chem 2004; 69: 3997-4000. (Pubitemid 38668270)
    • (2004) Journal of Organic Chemistry , vol.69 , Issue.11 , pp. 3997-4000
    • Rudolph, J.1    Hermanns, N.2    Bolm, C.3
  • 27
    • 33745760081 scopus 로고    scopus 로고
    • Catalytic asymmetric approaches towards enantiomerically enriched diarylmethanols and diarylmethylamines
    • DOI 10.1039/b600091f
    • Schmidt F, Stemmler RT, Rudolp J, Bolm C,. Catalytic asymmetric approaches towards enantiomerically enriched diarylmethanols and diarylmethylamines. Chem Soc Rev 2006; 35: 454-470. (Pubitemid 44009972)
    • (2006) Chemical Society Reviews , vol.35 , Issue.5 , pp. 454-470
    • Schmidt, F.1    Stemmler, R.T.2    Rudolph, J.3    Bolm, C.4
  • 28
    • 33645036043 scopus 로고    scopus 로고
    • Resolution of racemic 2-aminocyclohexanol derivatives and their application as ligands in asymmetric catalysis
    • Schiffers I, Rantanen T, Schmidt F, Bergmans W, Zani L, Bolm C,. Resolution of racemic 2-aminocyclohexanol derivatives and their application as ligands in asymmetric catalysis. J Org Chem 2006; 71: 2320-2331.
    • (2006) J Org Chem , vol.71 , pp. 2320-2331
    • Schiffers, I.1    Rantanen, T.2    Schmidt, F.3    Bergmans, W.4    Zani, L.5    Bolm, C.6
  • 29
    • 34547173727 scopus 로고    scopus 로고
    • Diarylmethanols by catalyzed asymmetric aryl transfer reactions onto aldehydes using boronic acids as aryl source
    • Schmid F, Rudolph J, Bolm C,. Diarylmethanols by catalyzed asymmetric aryl transfer reactions onto aldehydes using boronic acids as aryl source. Adv Synth Catal 2007; 349: 703-708.
    • (2007) Adv Synth Catal , vol.349 , pp. 703-708
    • Schmid, F.1    Rudolph, J.2    Bolm, C.3
  • 30
    • 35949001585 scopus 로고    scopus 로고
    • Application of β-hydroxysulfoximines in catalytic asymmetric phenyl transfer reactions for the synthesis of diarylmethanols
    • DOI 10.1021/jo7016718
    • Sedelmeier J, Bolm C,. Application of β-hydroxysulfoximines in catalytic asymmetric phenyl transfer reactions for the synthesis of diarylmethanols. J Org Chem 2007; 72: 8859-8862. (Pubitemid 350071716)
    • (2007) Journal of Organic Chemistry , vol.72 , Issue.23 , pp. 8859-8862
    • Sedelmeier, J.1    Bolm, C.2
  • 31
    • 75449086980 scopus 로고    scopus 로고
    • Chiral 1,1′-binaphthylazepine-derived amino alcohol catalyzed asymmetric aryl transfer reactions with boroxine as aryl source
    • Liu C, Guo ZL, Weng J,. Chiral 1,1′-binaphthylazepine-derived amino alcohol catalyzed asymmetric aryl transfer reactions with boroxine as aryl source. Chirality 2009; 22: 159-164.
    • (2009) Chirality , vol.22 , pp. 159-164
    • Liu, C.1    Guo, Z.L.2    Weng, J.3
  • 32
    • 0033546095 scopus 로고    scopus 로고
    • The first highly enantioselective catalytic diphenylzinc additions to aldehydes: Synthesis of chiral diarylcarbinols by asymmetric catalysis
    • Huang WS, Pu L,. The first highly enantioselective catalytic diphenylzinc additions to aldehydes: synthesis of chiral diarylcarbinols by asymmetric catalysis. J Org Chem 1999; 64: 4222-4223.
    • (1999) J Org Chem , vol.64 , pp. 4222-4223
    • Huang, W.S.1    Pu, L.2
  • 33
    • 0001140918 scopus 로고    scopus 로고
    • A highly general catalyst for the enantioselective reaction of aldehydes with diethylzinc
    • Huang WS, Hu QS, Pu L,. A highly general catalyst for the enantioselective reaction of aldehydes with diethylzinc. J Org Chem 1998; 63: 1364-1365.
    • (1998) J Org Chem , vol.63 , pp. 1364-1365
    • Huang, W.S.1    Hu, Q.S.2    Pu, L.3
  • 34
    • 0034620204 scopus 로고    scopus 로고
    • New and improved ligands for highly enantioselective catalytic diphenylzinc additions to aryl aldehydes
    • Huang WS, Pu L,. New and improved ligands for highly enantioselective catalytic diphenylzinc additions to aryl aldehydes. Tetrahedron Lett 1999; 41: 145-149.
    • (1999) Tetrahedron Lett , vol.41 , pp. 145-149
    • Huang, W.S.1    Pu, L.2
  • 35
    • 0013292139 scopus 로고    scopus 로고
    • Enantioselective additions of diethylzinc and diphenylzinc to aldehydes using 2-dialkyl-aminomethyl-2'-hydroxy-1, 1'-binaphthyls
    • Ko DH, Kim KH, Ha DC,. Enantioselective additions of diethylzinc and diphenylzinc to aldehydes using 2-dialkyl-aminomethyl-2'-hydroxy-1, 1'-binaphthyls. Organic Lett 2002; 4: 3759-3762.
    • (2002) Organic Lett , vol.4 , pp. 3759-3762
    • Ko, D.H.1    Kim, K.H.2    Ha, D.C.3
  • 36
    • 34247107487 scopus 로고    scopus 로고
    • Asymmetric diethylzinc addition and phenyl transfer to aldehydes using chiral cis-cyclopropane-based amino alcohols
    • DOI 10.1016/j.tetasy.2007.03.006, PII S0957416607001930
    • Zhong J, Guo H, Wang M, Yin M, Wang M,. Asymmetric diethylzinc addition and phenyl transfer to aldehydes using chiral cis-cyclopropane-based amino alcohols. Tetrahedron Asymmetry 2007; 18: 734-741. (Pubitemid 46590724)
    • (2007) Tetrahedron Asymmetry , vol.18 , Issue.6 , pp. 734-741
    • Zhong, J.1    Guo, H.2    Wang, M.3    Yin, M.4    Wang, M.5
  • 37
    • 48249152595 scopus 로고    scopus 로고
    • Structural optimization of enantiopure 2-cyclialkylamino-2-aryl-1,1- diphenylethanols as catalytic ligands for enantioselective additions to aldehydes
    • Escrich SR, Reddy KS, Jimeno C, Colet G, Pericàs MA,. Structural optimization of enantiopure 2-cyclialkylamino-2-aryl-1,1-diphenylethanols as catalytic ligands for enantioselective additions to aldehydes. J Org Chem 2008; 73: 5340-5353.
    • (2008) J Org Chem , vol.73 , pp. 5340-5353
    • Escrich, S.R.1    Reddy, K.S.2    Jimeno, C.3    Colet, G.4    Pericàs, M.A.5
  • 38
    • 33746311324 scopus 로고    scopus 로고
    • From aryl bromides to enantioenriched benzylic alcohols in a single flask: Catalytic asymmetric arylation of aldehydes
    • DOI 10.1002/anie.200600741
    • Kim JG, Walsh PJ,. From aryl bromides to enantioenriched benzylic alcohols in a single flask: catalytic asymmetric arylation of aldehydes. Angew Chem Int Ed 2006; 45: 4175-4178. (Pubitemid 44105677)
    • (2006) Angewandte Chemie - International Edition , vol.45 , Issue.25 , pp. 4175-4178
    • Kim, J.G.1    Walsh, P.J.2
  • 39
    • 40949084744 scopus 로고    scopus 로고
    • General method for the expedient synthesis of salt-free diorganozinc reagents using zinc methoxide
    • DOI 10.1021/ja710864p
    • Cote A, Charette AB,. General method for the expedient synthesis of salt-free diorganozinc reagents using zinc methoxide. J Am Chem Soc 2008; 130: 2771-2773. (Pubitemid 351416233)
    • (2008) Journal of the American Chemical Society , vol.130 , Issue.9 , pp. 2771-2773
    • Cote, A.1    Charette, A.B.2
  • 41
    • 13244253840 scopus 로고    scopus 로고
    • Highly enantioselective phenyl transfer to aryl aldehydes catalyzed by easily accessible chiral tertiary aminonaphthol
    • DOI 10.1021/jo048395i
    • Ji JX, Wu J, Yeung TTLA, Yip CW, Haynes RK, Chan ASC,. Highly enantioselective phenyl transfer to aryl aldehydes catalyzed by easily accessible chiral tertiary aminonaphthol. J Org Chem 2005; 70: 1093-1095. (Pubitemid 40189533)
    • (2005) Journal of Organic Chemistry , vol.70 , Issue.3 , pp. 1093-1095
    • Ji, J.-X.1    Wu, J.2    Au-Yeung, T.T.-L.3    Yip, C.-W.4    Haynes, R.K.5    Chan, A.S.C.6
  • 42
    • 0034714099 scopus 로고    scopus 로고
    • A practical o-hydroxybenzylamines promoted enantioselective addition of dialkylzincs to aldehydes with asymmetric amplification
    • Palmieri G,. A practical o-hydroxybenzylamines promoted enantioselective addition of dialkylzincs to aldehydes with asymmetric amplification. Tetrahedron Asymmetry 2000; 11: 3361-3373.
    • (2000) Tetrahedron Asymmetry , vol.11 , pp. 3361-3373
    • Palmieri, G.1
  • 43
    • 0035854305 scopus 로고    scopus 로고
    • Solvent-free asymmetric aminoalkylation of electron-rich aromatic compounds: Stereoselective synthesis of aminoalkylnaphthols by crystallization-induced asymmetric transformation
    • DOI 10.1021/jo0101205
    • Cimarelli C, Mazzanti A, Palmieri G, Volpini E,. Solvent-free asymmetric aminoalkylation of electron-rich aromatic compounds: stereoselective synthesis of aminoalkylnaphthols by crystallization-induced asymmetric transformation. J Org Chem 2001; 66: 4759-4765. (Pubitemid 32861787)
    • (2001) Journal of Organic Chemistry , vol.66 , Issue.14 , pp. 4759-4765
    • Cimarelli, C.1    Mazzanti, A.2    Palmieri, G.3    Volpini, E.4
  • 44
    • 0013035824 scopus 로고    scopus 로고
    • The application of chiral aminonaphthols in the enantioselective addition of diethylzinc to aryl aldehydes
    • DOI 10.1021/ol016341e
    • Liu DX, Zhang LC, Wang Q, Da CS, Xin ZQ, Wang R, Choi MCK, Chan ASC,. The application of chiral aminonaphthols in the enantioselective addition of diethylzinc to aryl aldehydes. Organic Lett 2001; 3: 2733-2735. (Pubitemid 33625284)
    • (2001) Organic Letters , vol.3 , Issue.17 , pp. 2733-2735
    • Liu, D.-X.1    Zhang, L.-C.2    Wang, Q.3    Da, C.-C.4    Xin, Z.-Q.5    Wang, R.6    Choi, M.C.K.7    Chan, A.S.C.8
  • 45
    • 0041806596 scopus 로고    scopus 로고
    • Phenyl versus ethyl transfer in the addition of organozinc reagents to aldehydes: A theoretical study
    • DOI 10.1002/anie.200351150
    • Rudolph J, Rasmussen T, Bolm C, Norrby PO,. Phenyl versus ethyl transfer in the addition of organozinc reagents to aldehydes: a theoretical study. Angew Chem Int Ed 2003; 42: 3002-3005. (Pubitemid 36897003)
    • (2003) Angewandte Chemie - International Edition , vol.42 , Issue.26 , pp. 3002-3005
    • Rudolph, J.1    Rasmussen, T.2    Bolm, C.3    Norrby, P.-O.4
  • 46
    • 1842503817 scopus 로고    scopus 로고
    • 2-Piperidino-1,1,2-triphenylethanol: A Highly Effective Catalyst for the Enantioselective Arylation of Aldehydes
    • DOI 10.1021/jo035824o
    • Fontes M, Verdaguer X, Sola L, Pericàs MA, Riera A,. 2-piperidino-1,1,2-triphenylethanol: a highly effective catalyst for the enantioselective arylation of aldehydes. J Org Chem 2004; 69: 2532-2543. (Pubitemid 38419070)
    • (2004) Journal of Organic Chemistry , vol.69 , Issue.7 , pp. 2532-2543
    • Fontes, M.1    Verdaguer, X.2    Sola, L.3    Pericas, M.A.4    Riera, A.5
  • 47
    • 13444261987 scopus 로고    scopus 로고
    • New insights into the stereoselectivity of the aryl zinc addition to aldehydes
    • DOI 10.1021/ja046254s
    • Rudolph J, Bolm C, Norrby PO,. New Insights into the stereoselectivity of the aryl zinc addition to aldehydes. J Am Chem Soc 2005; 127: 1548-1552. (Pubitemid 40204530)
    • (2005) Journal of the American Chemical Society , vol.127 , Issue.5 , pp. 1548-1552
    • Rudolph, J.1    Bolm, C.2    Norrby, P.-O.3
  • 48
    • 22044454886 scopus 로고    scopus 로고
    • Enantioselective alkynylation and phenylation of aromatic aldehydes promoted by atropisomeric 1,1′-binaphthylazepine-based amino alcohols
    • DOI 10.1016/j.tetasy.2005.05.028, PII S0957416605004040
    • Pizzuti MG, Superchi S,. Enantioselective alkynylation and phenylation of aromatic aldehydes promoted by atropisomeric 1,10-binaphthylazepine-based amino alcohols. Tetrahedron Asymmetry 2005; 16: 2263-2269. (Pubitemid 40967881)
    • (2005) Tetrahedron Asymmetry , vol.16 , Issue.13 , pp. 2263-2269
    • Pizzuti, M.G.1    Superchi, S.2


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