-
1
-
-
0023025052
-
Stereochemistry:A source of problems in medicinal chemistry
-
Ariens, E. J. Stereochemistry: A source of problems in medicinal chemistry. Med. Res. Rev. 1986, 6, 451;
-
(1986)
Med. Res. Rev
, vol.6
, pp. 451
-
-
Ariens, E.J.1
-
2
-
-
0002312023
-
Drug chirality-scaleup, manufacturing, and control
-
Federsel, H. J. Drug chirality-scaleup, manufacturing, and control. Chemtech. 1993, 23, 24.
-
(1993)
Chemtech
, vol.23
, pp. 24
-
-
Federselh., J.1
-
3
-
-
0029588274
-
Application of a practical biocatalytic reduction to an enantioselective synthesis of the 5H-2,3-benzodiazepine LY300164
-
Anderson, B. A.; Hansen, M. M.; Harkness, A. R.; Henry, C. L.; Vicenzi, J. T.; Zmijewski, M. J. Application of a practical biocatalytic reduction to an enantioselective synthesis of the 5H-2,3-benzodiazepine LY300164. J. Am. Chem. Soc. 1995, 117, 12358.
-
(1995)
J. Am. Chem. Soc
, vol.117
, pp. 12358
-
-
Anderson, B.A.1
Hansen, M.M.2
Harkness, A.R.3
Henry, C.L.4
Vicenzi, J.T.5
Zmijewski, M.J.6
-
4
-
-
33947205982
-
A new enzymatic approach to (R)-tamsulosin hydro-chloride
-
Acetti, D.; Brenna, E.; Fuganti, C. A new enzymatic approach to (R)-tamsulosin hydro-chloride. Tetrahedron: Asymmetry 2007, 18, 488.
-
(2007)
Tetrahedron: Asymmetry
, vol.18
, pp. 488
-
-
Acetti, D.1
Brenna, E.2
Fuganti, C.3
-
5
-
-
0043201072
-
Stereospecific synthesis of amphetamines
-
Wagner, J. M.; McElhinny, C. J.; Lewin, A. H.; Carroll, F. I. Stereospecific synthesis of amphetamines. Tetrahedron: Asymmetry 2003, 14, 2119;
-
(2003)
Tetrahedron: Asymmetry
, vol.14
, pp. 2119
-
-
Wagner, J.M.1
McElhinny, C.J.2
Lewin, A.H.3
Carroll, F.I.4
-
6
-
-
0025234715
-
A structure-affinity study of the binding of 4-substituted analogues of 1-(2,5-dimethoxyphenyl)-2-aminopropane at 5-HT2 serotonin receptors
-
Seggel, M. R.; Yousif, M. Y.; Lyon, R. A.; Titeler, M.; Roth, B. L.; Suba, E. A.; Glennon, R. A. A structure-affinity study of the binding of 4-substituted analogues of 1-(2,5-dimethoxyphenyl)-2-aminopropane at 5-HT2 serotonin receptors. J. Med. Chem. 1990, 33, 1032;
-
(1990)
J. Med. Chem
, vol.33
, pp. 1032
-
-
Seggel, M.R.1
Yousif, M.Y.2
Lyon, R.A.3
Titeler, M.4
Roth, B.L.5
Suba, E.A.6
Glennon, R.A.7
-
7
-
-
0033966528
-
Hair analysis by using radioimmunoassay high performance liquid chromatography and capillary electrophoresis to investigate chronic exposure to heroin, cocaine, and=or ecstasy in applicants for driving licenses
-
Tagliaro, F.; Valentini, R.; Manetto, G.; Crivellente, F.; Carli, G.; Marigo, M. Hair analysis by using radioimmunoassay high performance liquid chromatography and capillary electrophoresis to investigate chronic exposure to heroin, cocaine, and=or ecstasy in applicants for driving licenses. Forensic Sci. Int. 2000, 107, 121.
-
(2000)
Forensic Sci. Int
, vol.107
, pp. 121
-
-
Tagliaro, F.1
Valentini, R.2
Manetto, G.3
Crivellente, F.4
Carli, G.5
Marigo, M.6
-
8
-
-
33846554941
-
Enantioselective synthesis of 3-methylisochromans and determination of their absolute configurations by circular dichroism
-
Kerti, G.; Kurtan, T.; Illyes, T.-Z.; Kover, K. E.; Solyom, S.; Pescitelli, G.; Fujioka, N.; Berova, N.; Antus, S. Enantioselective synthesis of 3-methylisochromans and determination of their absolute configurations by circular dichroism. Eur. J. Org. Chem. 2007, 296;
-
(2007)
Eur. J. Org. Chem
, vol.296
-
-
Kerti, G.1
Kurtan, T.2
Illyes, T.-Z.3
Kover, K.E.4
Solyom, S.5
Pescitelli, G.6
Fujioka, N.7
Berova, N.8
Antus, S.9
-
9
-
-
34249987145
-
Asymmetric synthesis of 3-substituted 8-hydroxy-3,4-dihydroisocoumarins from (S)-4-isopropyl-2-(2-methoxy-6-methylphenyl) oxazoline
-
Uchida, K.; Fukuda, T.; Iwao, M. Asymmetric synthesis of 3-substituted 8-hydroxy-3,4-dihydroisocoumarins from (S)-4-isopropyl-2-(2-methoxy-6- methylphenyl) oxazoline. Tetrahedron 2007, 63, 7178.
-
(2007)
Tetrahedron
, vol.63
, pp. 7178
-
-
Uchida, K.1
Fukuda, T.2
Iwao, M.3
-
10
-
-
0034737427
-
Synthetic strategies towards pyrano-naphthoquinone antibiotics
-
Brimble, M. A.; Nairn, M. R.; Prabaharan, H. Synthetic strategies towards pyrano-naphthoquinone antibiotics. Tetrahedron 2000, 56, 1937;
-
(2000)
Tetrahedron
, vol.56
, pp. 1937
-
-
Brimble, M.A.1
Nairn, M.R.2
Prabaharan, H.3
-
11
-
-
0036206928
-
Pigments of fungi, part 68: Synthesis and absolute configuration of thysanone
-
Donner, C. D.; Gill, M. Pigments of fungi, part 68: Synthesis and absolute configuration of thysanone. J. Chem. Soc., Perkin Trans. 1 2002, 938.
-
(2002)
J. Chem. Soc., Perkin Trans.
, vol.1
, pp. 938
-
-
Donner, C.D.1
Gill, M.2
-
12
-
-
58249114210
-
Organocatalytic enantioselective formal synthesis of HRV 3C-protease inhibitor (1R,3S)-thysanone
-
Sawant, R. T.; Waghmode, S. B. Organocatalytic enantioselective formal synthesis of HRV 3C-protease inhibitor (1R,3S)-thysanone. Tetrahedron 2009, 65, 1599.
-
(2009)
Tetrahedron
, vol.65
, pp. 1599
-
-
Sawant, R.T.1
Waghmode, S.B.2
-
13
-
-
0037423131
-
Amano PS-catalysed enantioselective acylation of (±)-a-methyl-1,3- benzodioxole-5-ethanol: An efficient resolution of chiral intermediates of the remarkable antiepileptic drug candidate, (\)-talampanel
-
Easwar, S.; Argade, N. P. Amano PS-catalysed enantioselective acylation of (±)-a-methyl-1,3-benzodioxole-5-ethanol: An efficient resolution of chiral intermediates of the remarkable antiepileptic drug candidate, (\)-talampanel. Tetrahedron: Asymmetry 2003,14, 333;
-
(2003)
Tetrahedron: Asymmetry
, vol.14
, pp. 333
-
-
Easwar, S.1
Argade, N.P.2
-
14
-
-
33748804169
-
Kinetic and chemical resolution of different 1-phenyl-2-propanol derivatives
-
Kiss, V.; Egri, G.; Balint, J.; Ling, I.; Barkoczi, J.; Fogassy, E. Kinetic and chemical resolution of different 1-phenyl-2-propanol derivatives. Tetrahedron: Asymmetry 2007, 17, 2220.
-
(2007)
Tetrahedron: Asymmetry
, vol.17
, pp. 2220
-
-
Kiss, V.1
Egri, G.2
Balint, J.3
Ling, I.4
Barkoczi, J.5
Fogassy, E.6
-
15
-
-
0021512929
-
Rational designing of efficient chiral reducing agents: Highly enantioselective of aromatic ketones by binaphthol-modified lithium aluminum hydride reagents reduction
-
Noyori, R.; Tomino, I.; Tanimoto, Y.; Nishizawa, M. Rational designing of efficient chiral reducing agents: Highly enantioselective of aromatic ketones by binaphthol-modified lithium aluminum hydride reagents reduction. J. Am. Chem. Soc. 1984, 106, 6709;
-
(1984)
J. Am. Chem. Soc
, vol.106
, pp. 6709
-
-
Noyori, R.1
Tomino, I.2
Tanimoto, Y.3
Nishizawa, M.4
-
16
-
-
33751385619
-
Stereocontrolled catalytic asymmetric reduction of ketones with oxazaborolidines derived from new chiral amino alcohols
-
Kim, Y. H.; Park, D. H.; Byun, I. S.; Yoon, I. K.; Park, C. S. Stereocontrolled catalytic asymmetric reduction of ketones with oxazaborolidines derived from new chiral amino alcohols. J. Org. Chem. 1993, 58, 4511;
-
(1993)
J. Org. Chem
, vol.58
, pp. 4511
-
-
Kim, Y.H.1
Park, D.H.2
Byun, I.S.3
Yoon, I.K.4
Park, C.S.5
-
17
-
-
37049067035
-
Asymmetric hydride reduction using a chiral aluminium reagent modified by a crowned 2,2'-dihydroxy-1,1'-binaphthyl
-
Yamamoto, K.; Ueno, K.; Naemura, K. Asymmetric hydride reduction using a chiral aluminium reagent modified by a crowned 2,2'-dihydroxy-1,1'-binaphthyl. J. Chem. Soc, Perkin Trans. 1 1991, 2607.
-
(1991)
J. Chem. Soc, Perkin Trans.
, vol.1
, pp. 2607
-
-
Yamamoto, K.1
Ueno, K.2
Naemura, K.3
-
18
-
-
23644444887
-
Production of (R)-chiral alcohols by a hydrogen-transfer bioreduction with NADH-dependent Leifsonia alcohol dehydrogenase (LSADH)
-
Inoue, K.; Makino, Y.; Itoh, N. Production of (R)-chiral alcohols by a hydrogen-transfer bioreduction with NADH-dependent Leifsonia alcohol dehydrogenase (LSADH). Tetrahedron Asymmetry 2005,16, 2539;
-
(2005)
Tetrahedron Asymmetry
, vol.16
, pp. 2539
-
-
Inoue, K.1
Makino, Y.2
Itoh, N.3
-
19
-
-
32444436675
-
Stereoselective production of (S)-1-araalkyl-and 1-arylethanols by freshly harvested and lyophilized yeast cells
-
Erdelyi, B.; Szabo, A.; Seres, G.; Birincsik, L.; Ivanics, J.; Szatzkerd, G.; Popped, L. Stereoselective production of (S)-1-araalkyl-and 1-arylethanols by freshly harvested and lyophilized yeast cells. Tetrahedron: Asymmetry 2006, 17, 268.
-
(2006)
Tetrahedron: Asymmetry
, vol.17
, pp. 268
-
-
Erdelyi, B.1
Szabo, A.2
Seres, G.3
Birincsik, L.4
Ivanics, J.5
Szatzkerd, G.6
Popped, L.7
-
20
-
-
34547738969
-
An organo-catalytic approach to the enantioselective synthesis of (R)-selegiline
-
Talluri, S. K.; Sudalai, A. An organo-catalytic approach to the enantioselective synthesis of (R)-selegiline. Tetrahedron 2007, 63, 9758.
-
(2007)
Tetrahedron
, vol.63
, pp. 9758
-
-
Talluri, S.K.1
Sudalai, A.2
-
21
-
-
6044269452
-
In the golden age of organocatalysis
-
Dalko, P. I.; Moisan, L. In the golden age of organocatalysis. Angew. Chem. Int. Ed. 2004, 43, 5138;
-
(2004)
Angew. Chem. Int. Ed
, vol.43
, pp. 5138
-
-
Dalko, P.I.1
Moisan, L.2
-
22
-
-
4143094833
-
Asymmetric organocatalysis
-
Houk, K. N.; List, B. Asymmetric organocatalysis. Acc. Chem. Res. 2004, 37, 487;
-
(2004)
Acc. Chem. Res
, vol.37
, pp. 487
-
-
Houk, K.N.1
List, B.2
-
23
-
-
15244343428
-
Asymmetric organocatalysis
-
List, B.; Seayad, J. Asymmetric organocatalysis. Org. Biomol. Chem. 2005, 3, 719.
-
(2005)
Org. Biomol. Chem
, vol.3
, pp. 719
-
-
List, B.1
Seayad, J.2
-
25
-
-
0037043180
-
Proline-catalyzed asymmetric reactions
-
List, B. Proline-catalyzed asymmetric reactions. Tetrahedron 2002, 58, 5573;
-
(2002)
Tetrahedron
, vol.58
, pp. 5573
-
-
List, B.1
-
26
-
-
4143095871
-
The simplest "enzyme'' enamine catalysis is a powerful strategy for the catalytic generation and use of carbanion equivalents
-
List, B. The simplest "enzyme'' enamine catalysis is a powerful strategy for the catalytic generation and use of carbanion equivalents. Acc. Chem. Res. 2004, 37, 548;
-
(2004)
Acc. Chem. Res
, vol.37
, pp. 548
-
-
List, B.1
-
28
-
-
0141957357
-
Direct proline-catalyzed asymmetric a-aminooxylation of aldehydes
-
Hayashi, Y.; Yamaguchi, J.; Hibino, K.; Shoji, M. Direct proline-catalyzed asymmetric a-aminooxylation of aldehydes. Tetrahedron Lett. 2003, 44, 8293;
-
(2003)
Tetrahedron Lett
, vol.44
, pp. 8293
-
-
Hayashi, Y.1
Yamaguchi, J.2
Hibino, K.3
Shoji, M.4
-
29
-
-
0141522552
-
A facile and rapid route to highly enantiopure 1,2-diols by novel catalytic asymmetric a-aminoxylation of aldehydes
-
Zhong, G. A facile and rapid route to highly enantiopure 1,2-diols by novel catalytic asymmetric a-aminoxylation of aldehydes. Angew. Chem. Int. Ed. 2003, 42, 4247;
-
(2003)
Angew. Chem. Int. Ed
, vol.42
, pp. 4247
-
-
Zhong, G.1
-
30
-
-
0041733541
-
The direct and enantioselective organo-catalytic a-oxidation of aldehydes
-
Brown, S. P.; Brochu, M. P.; Sinz, C. J.; MacMillan, D. W. C. The direct and enantioselective organo-catalytic a-oxidation of aldehydes. J. Am. Chem. Soc. 2003, 125, 10808;
-
(2003)
J. Am. Chem. Soc
, vol.125
, pp. 10808
-
-
Brown, S.P.1
Brochu, M.P.2
Sinz, C.J.3
MacMillan, D.W.C.4
-
31
-
-
4344693780
-
Direct proline-catalyzed asymmetric a-aminoxylation of aldehydes and ketones
-
Hayashi, Y.; Yamaguchi, J.; Sumiya, T.; Hibino, K.; Shoji, M. Direct proline-catalyzed asymmetric a-aminoxylation of aldehydes and ketones. J. Org. Chem. 2004, 69, 5966.
-
(2004)
J. Org. Chem
, vol.69
, pp. 5966
-
-
Hayashi, Y.1
Yamaguchi, J.2
Sumiya, T.3
Hibino, K.4
Shoji, M.5
-
32
-
-
37049067118
-
EPR studies on the photofragmentation of 2,2-dialkyl-2- alkylaminoacetophenones
-
For 2a, see Leopold, D.; Fischer, H. EPR studies on the photofragmentation of 2,2-dialkyl-2-alkylaminoacetophenones. J. Chem. Soc, Perkin Trans. 2 1992, 513;
-
(1992)
J. Chem. Soc, Perkin Trans.
, vol.2
, pp. 513
-
-
Leopold, D.1
Fischer, H.2
-
33
-
-
37049106574
-
Synthesis of (±)-[6]-gingerol (pungent principle of ginger) and relatives via directed aldol reactions
-
for 2b, see Denniff, P.; Whiting, D. A. Synthesis of (±)-[6]- gingerol (pungent principle of ginger) and relatives via directed aldol reactions. J. Chem. Soc, Chem. Commun. 1976, 712
-
(1976)
J. Chem. Soc, Chem. Commun
, pp. 712
-
-
Denniff, P.1
Whiting, D.A.2
-
34
-
-
0034740850
-
Three-component synthesis of (E)-a,b-unsaturated amides of the piperine family
-
for 2c, see Schobert, R.; Siegfried, S.; Gordon, G. J. Three-component synthesis of (E)-a,b-unsaturated amides of the piperine family. J. Chem. Soc, Perkin Trans. 1 2001, 2393
-
(2001)
J. Chem. Soc, Perkin Trans.
, vol.1
, pp. 2393
-
-
Schobert, R.1
Siegfried, S.2
Gordon, G.J.3
-
35
-
-
35548973554
-
Tandem molybdenum-catalyzed hydrosilylations: An expedient synthesis of b-aryl aldehydes
-
for 2d, see Frost, C. G.; Hartley, B. C. Tandem molybdenum-catalyzed hydrosilylations: An expedient synthesis of b-aryl aldehydes. Org. Lett. 2007, 9, 4259
-
(2007)
Org. Lett
, vol.9
, pp. 4259
-
-
Frost, C.G.1
Hartley, B.C.2
-
36
-
-
0037051615
-
Catalytic regioselective sulfonylation of a-chelatable alcohols: Scope and mechanistic insight
-
Martinelli, M. J.; Vaidyanathan, R.; Pawlak, J. M.; Nayyar, N. K.; Dhokte, U. P.; Doecke, C. W.; Zollars, L. M. H.; Moher, E. D.; Khau, V. V.; Kosmrlj, B. Catalytic regioselective sulfonylation of a-chelatable alcohols: Scope and mechanistic insight. J. Am. Chem. Soc. 2002, 124, 3758.
-
(2002)
J. Am. Chem. Soc
, vol.124
, pp. 3758
-
-
Martinelli, M.J.1
Vaidyanathan, R.2
Pawlak, J.M.3
Nayyar, N.K.4
Dhokte, U.P.5
Doecke, C.W.6
Zollars, L.M.H.7
Moher, E.D.8
Khau, V.V.9
Kosmrlj, B.10
-
37
-
-
33751428917
-
Short and practical enantioselective synthesis of linezolid and eperezolid via proline-catalyzed asymmetric a-aminooxylation
-
For 3a, Narina, S. V.; Talluri, S. K.; George, S.; Sudalai, A. Short and practical enantioselective synthesis of linezolid and eperezolid via proline-catalyzed asymmetric a-aminooxylation. Tetrahedron Lett. 2007, 48, 65;
-
(2007)
Tetrahedron Lett
, vol.48
, pp. 65
-
-
Narina, S.V.1
Talluri, S.K.2
George, S.3
Sudalai, A.4
-
38
-
-
0033402069
-
Antioxidative phenylpropanoids from berries of Pimenta dioica
-
Hiroe, K.; Sanae, H.; Yayoi, K.; Nobuji, N. Antioxidative phenylpropanoids from berries of Pimenta dioica. Phytochemistry 1999, 52, 1307;
-
(1999)
Phytochemistry
, vol.52
, pp. 1307
-
-
Hiroe, K.1
Sanae, H.2
Yayoi, K.3
Nobuji, N.4
-
39
-
-
0000067123
-
Polyphenolic acids of Lithospermum ruderale (Boraginaceae), I: Isolation and structure determination of lithospermic acid
-
Kelley, C. J.; Mahajan, J. R.; Brooks, L. C.; Neubert, L. A.; Breneman, W. R.; Carmack, M. Polyphenolic acids of Lithospermum ruderale (Boraginaceae), I: Isolation and structure determination of lithospermic acid. J. Org. Chem. 1975, 40, 1804
-
(1975)
J. Org. Chem.
, vol.40
, pp. 1804
-
-
Kelley, C.J.1
Mahajan, J.R.2
Brooks, L.C.3
Neubert, L.A.4
Breneman, W.R.5
Carmack, M.6
-
40
-
-
77954508088
-
Enantioselective synthesis of (R)-(\+)-safrole oxide
-
Rama, M. H.; Rao, A. S. Enantioselective synthesis of (R)-(\+)-safrole oxide. Indian J. Chem. 1998, 37B, 78
-
(1998)
Indian J. Chem.
, vol.37 B
, pp. 78
-
-
Rama, M.H.1
Rao, A.S.2
-
41
-
-
0030575837
-
On the stereochemistry of the Baeyer-Villiger degradation of arylalk-ylketones structurally related to raspberry ketone by Beauveria bassiana
-
For 1a, see Ref. 3; Donzelli, F.; Fuganti, C.; Mendozza, M.; Pedrocchi-Fantoni, G.; Servi, S.; Zucchi, G. On the stereochemistry of the Baeyer-Villiger degradation of arylalk-ylketones structurally related to raspberry ketone by Beauveria bassiana. Tetrahedron Asymmetry 1996, 7, 3129
-
(1996)
Tetrahedron Asymmetry
, vol.7
, pp. 3129
-
-
Donzelli, F.1
Fuganti, C.2
Mendozza, M.3
Pedrocchi-Fantoni, G.4
Servi, S.5
Zucchi, G.6
|