-
1
-
-
5444241700
-
-
Optically active alcohols for liquid crystal compositions used in display devices. EP270244, 1988
-
(a) Ohno K, Saito S, Miyazawa K, Ushioda M, Inoue H, Yoshida N. Optically active alcohols for liquid crystal compositions used in display devices. EP270244, 1988 (Chem Abstr 1989;110:31528x).
-
(1989)
Chem Abstr
, vol.110
-
-
Ohno, K.1
Saito, S.2
Miyazawa, K.3
Ushioda, M.4
Inoue, H.5
Yoshida, N.6
-
2
-
-
3042523037
-
-
Liquid crystal compound having branched methyl group, liquid crystal composition containing it, and display using it. JP2001114722, 2001
-
(b) Koizumi Y, Matsui S, Takeuchi H, Kubo Y, Nakagawa E. Liquid crystal compound having branched methyl group, liquid crystal composition containing it, and display using it. JP2001114722, 2001 (Chem Abstr 2001;134:3187810.
-
(2001)
Chem Abstr
, vol.134
, pp. 3187810
-
-
Koizumi, Y.1
Matsui, S.2
Takeuchi, H.3
Kubo, Y.4
Nakagawa, E.5
-
3
-
-
0001087017
-
Preparation of chiral 1-phenylethanols and bromides
-
(a) Stein AR, Dawe RD, Sweet JR. Preparation of chiral 1-phenylethanols and bromides. Can J Chem 1985;63:3442.
-
(1985)
Can J Chem
, vol.63
, pp. 3442
-
-
Stein, A.R.1
Dawe, R.D.2
Sweet, J.R.3
-
5
-
-
0036638083
-
Preperation of linear secondary alcohols of high optical purity through chemical resolution with chiral α-phenylethylamines
-
and citations therein
-
(c) Su XB, Zhang QH, Wu YQ, Xu JX. Preperation of linear secondary alcohols of high optical purity through chemical resolution with chiral α-phenylethylamines. Chin J Org Chem 2002;22:496-500 (and citations therein).
-
(2002)
Chin J Org Chem
, vol.22
, pp. 496-500
-
-
Su, X.B.1
Zhang, Q.H.2
Wu, Y.Q.3
Xu, J.X.4
-
6
-
-
0001677435
-
Side chain hydroxylation of aromatic compounds by fungi. 1. Products and stereochemistry
-
(a) Holland HL, Bergen EJ, Chenchaiah PC, Khan SH, Munoz B, Ninniss RW, Richards D. Side chain hydroxylation of aromatic compounds by fungi. 1. Products and stereochemistry. Can J Chem 1987; 65:502.
-
(1987)
Can J Chem
, vol.65
, pp. 502
-
-
Holland, H.L.1
Bergen, E.J.2
Chenchaiah, P.C.3
Khan, S.H.4
Munoz, B.5
Ninniss, R.W.6
Richards, D.7
-
7
-
-
0026014628
-
Resolution of secondary alcohols by enzyme-catalyzed transesterification in alkyl carboxylates as the solvent
-
(b) Janssen AJM, Klunder AJH, Zwanenburg B. Resolution of secondary alcohols by enzyme-catalyzed transesterification in alkyl carboxylates as the solvent. Tetrahedron 1991;47:7645.
-
(1991)
Tetrahedron
, vol.47
, pp. 7645
-
-
Janssen, A.J.M.1
Klunder, A.J.H.2
Zwanenburg, B.3
-
8
-
-
0026733927
-
Asymmetric syntheses with chiral oxazaborolidines
-
(a) Wallbaum S, Martens J. Asymmetric syntheses with chiral oxazaborolidines. Tetrahedron: Asymmetry 1992;3:1475.
-
(1992)
Tetrahedron: Asymmetry
, vol.3
, pp. 1475
-
-
Wallbaum, S.1
Martens, J.2
-
9
-
-
0026663693
-
Practical and useful methods for the enantioselective reduction of unsymmetrical ketones
-
(b) Singh VK. Practical and useful methods for the enantioselective reduction of unsymmetrical ketones. Synthesis 1992;605.
-
(1992)
Synthesis
, pp. 605
-
-
Singh, V.K.1
-
10
-
-
0342697384
-
Asymmetric boron-catalyzed reactions
-
(c) Deloux L, Srebnik M. Asymmetric boron-catalyzed reactions. Chem Rev 1993;93:763.
-
(1993)
Chem Rev
, vol.93
, pp. 763
-
-
Deloux, L.1
Srebnik, M.2
-
11
-
-
0032541271
-
Aminoacrylic compounds. Part 31. Reduction of carbonyl compounds with chiral oxazaborolidine catalysts: A new paradigm for enantioselective catalysis and a powerful new synthetic method
-
(d) Corey EJ, Helal CJ. Aminoacrylic compounds. Part 31. Reduction of carbonyl compounds with chiral oxazaborolidine catalysts: a new paradigm for enantioselective catalysis and a powerful new synthetic method. Angew Chem Int Ed 1998;37:1986-2012.
-
(1998)
Angew Chem Int Ed
, vol.37
, pp. 1986-2012
-
-
Corey, E.J.1
Helal, C.J.2
-
12
-
-
12044253833
-
Baker's yeast mediated transformations in organic chemistry
-
(a) Csuk R, Glanzer BI. Baker's yeast mediated transformations in organic chemistry. Chem Rev 1991;91:49.
-
(1991)
Chem Rev
, vol.91
, pp. 49
-
-
Csuk, R.1
Glanzer, B.I.2
-
13
-
-
0035808832
-
A facile synthesis of (R)-(-)-2-azido-1-arylethanols from 2-azido-arylketanes using baker's yeast
-
(b) Yadav JS, Reddy PT, Nanda S, Rao AB. A facile synthesis of (R)-(-)-2-azido-1-arylethanols from 2-azido-arylketanes using baker's yeast. Tetrahedron: Asymmetry 2001;12:63-67.
-
(2001)
Tetrahedron: Asymmetry
, vol.12
, pp. 63-67
-
-
Yadav, J.S.1
Reddy, P.T.2
Nanda, S.3
Rao, A.B.4
-
14
-
-
0037148449
-
Stereo-selective synthesis of (R)-(-)-denopamine, (R)-(-)-tembamide and (R)-(-)-aegeline via asymmetric reduction of azidoketones by Daucus carota in aqueous medium
-
(c) Yadav JS, Reddy PT, Nanda S, Rao AB. Stereo-selective synthesis of (R)-(-)-denopamine, (R)-(-)-tembamide and (R)-(-)-aegeline via asymmetric reduction of azidoketones by Daucus carota in aqueous medium. Tetrahedron: Asymmetry 2002;12: 3381-3385.
-
(2002)
Tetrahedron: Asymmetry
, vol.12
, pp. 3381-3385
-
-
Yadav, J.S.1
Reddy, P.T.2
Nanda, S.3
Rao, A.B.4
-
15
-
-
0030794772
-
β-Silyl diorganozinc compounds - A new class of useful zinc reagents
-
(a) Berger S, Langer F, Lutz C, Knochel P, Mobley TA, Reddy CK. β-Silyl diorganozinc compounds - A new class of useful zinc reagents. Angew Chem Int Ed 1997;36:1496-1498.
-
(1997)
Angew Chem Int Ed
, vol.36
, pp. 1496-1498
-
-
Berger, S.1
Langer, F.2
Lutz, C.3
Knochel, P.4
Mobley, T.A.5
Reddy, C.K.6
-
16
-
-
0031579454
-
Enantioselective addition of diethylzinc to aromatic aldehydes catalyzed by Ti(BINOL) complex
-
(b) Zhang FY, Yip CW, Cao R, Chan ASC. Enantioselective addition of diethylzinc to aromatic aldehydes catalyzed by Ti(BINOL) complex. Tetrahedron: Asymmetry 1997;8:585-589.
-
(1997)
Tetrahedron: Asymmetry
, vol.8
, pp. 585-589
-
-
Zhang, F.Y.1
Yip, C.W.2
Cao, R.3
Chan, A.S.C.4
-
17
-
-
0032573438
-
A simple, convenient preparation for enantiomerically pure 1,1′-bi-2-naphthols
-
(c) Shan ZX, Xiong Y, Li WZ, Zhao DJ. A simple, convenient preparation for enantiomerically pure 1,1′-bi-2-naphthols. Tetrahedron: Asymmetry 1998;9:3985-3989.
-
(1998)
Tetrahedron: Asymmetry
, vol.9
, pp. 3985-3989
-
-
Shan, Z.X.1
Xiong, Y.2
Li, W.Z.3
Zhao, D.J.4
-
18
-
-
0038771236
-
Preparation of high optically pure linear secondary alcohols via asymmetric reduction of prochiral ketones by borane
-
Xu JX, Su XB, Zhang QH. Preparation of high optically pure linear secondary alcohols via asymmetric reduction of prochiral ketones by borane. Tetrahedron: Asymmetry 2003;14:1781-1786.
-
(2003)
Tetrahedron: Asymmetry
, vol.14
, pp. 1781-1786
-
-
Xu, J.X.1
Su, X.B.2
Zhang, Q.H.3
-
19
-
-
0002636206
-
A practical for asymmetric borane reduction of prochiral ketones using chiral amino alcohols and trimethyl borate
-
Masui M, Shioiri T. A practical for asymmetric borane reduction of prochiral ketones using chiral amino alcohols and trimethyl borate. Synlett 1997;273-274.
-
(1997)
Synlett
, pp. 273-274
-
-
Masui, M.1
Shioiri, T.2
-
20
-
-
0346992396
-
Effect of temperature on the enantioselectivity in the oxazaborolidine-catalyzed asymmetric reduction of ketones. Non-catalytic borane reduction, a nonneglectable factor in reduction system
-
Xu JX, Wei TZ, Zhang QH. Effect of temperature on the enantioselectivity in the oxazaborolidine-catalyzed asymmetric reduction of ketones. Non-catalytic borane reduction, a nonneglectable factor in reduction system. J Org Chem 2003;68:10146-10151.
-
(2003)
J Org Chem
, vol.68
, pp. 10146-10151
-
-
Xu, J.X.1
Wei, T.Z.2
Zhang, Q.H.3
-
21
-
-
0037007663
-
Highly efficient synthesis of chiral beta-hydroxy sulfides with high enantiomeric purity via CBS-oxazaborolidine-catalyzed borane reduction
-
Cho BT, Choi OK, Kim DJ. Highly efficient synthesis of chiral beta-hydroxy sulfides with high enantiomeric purity via CBS-oxazaborolidine- catalyzed borane reduction. Tetrahedron: Asymmetry 2002;13: 697-703.
-
(2002)
Tetrahedron: Asymmetry
, vol.13
, pp. 697-703
-
-
Cho, B.T.1
Choi, O.K.2
Kim, D.J.3
-
22
-
-
24544440141
-
-
Preparation of α-halogenated alkylsulfonylacetophenones US 2,763,692, 1956
-
Gregory WA. Preparation of α-halogenated alkylsulfonylacetophenones. US 2,763,692, 1956 (Chem Abstr 1957;51:P4429c).
-
(1957)
Chem Abstr
, vol.51
-
-
Gregory, W.A.1
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