Diastereoselective reduction of chiral α-ketoamides derived from (S)-proline esters with sodium borohydride. Preparation of optically active α-hydroxy acids

Journal of the Chemical Society Perkin Transactions 1 ◽

10.1039/p19850000769 ◽

1985 ◽

pp. 769-772 ◽

Cited By ~ 5

Author(s):

Kenso Soai ◽

Hitoshi Hasegawa

Keyword(s):

Sodium Borohydride ◽

Optically Active ◽

Hydroxy Acids ◽

Diastereoselective Reduction

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ChemInform Abstract: DIASTEREOSELECTIVE REDUCTION OF CHIRAL α-KETOAMIDES DERIVED FROM (S)-PROLINE ESTERS WITH SODIUM BOROHYDRIDE. PREPARATION OF OPTICALLY ACTIVE α-HYDROXY ACIDS

Chemischer Informationsdienst ◽

10.1002/chin.198532062 ◽

1985 ◽

Vol 16 (32) ◽

Author(s):

K. SOAI ◽

H. HASEGAWA

Keyword(s):

Sodium Borohydride ◽

Optically Active ◽

Hydroxy Acids ◽

Diastereoselective Reduction

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ChemInform Abstract: Stereodivergent Synthesis of Optically Active α-Hydroxy Acids via Diastereoselective Reduction of α-Keto Esters Derived from L-Quebrachitol.

ChemInform ◽

10.1002/chin.199419257 ◽

2010 ◽

Vol 25 (19) ◽

pp. no-no

Author(s):

T. AKIYAMA ◽

H. NISHIMOTO ◽

T. KUWATA ◽

S. OZAKI

Keyword(s):

Optically Active ◽

Hydroxy Acids ◽

Keto Esters ◽

Diastereoselective Reduction

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Circular dichroic and absorption spectral studies on complexes of nickel(II) with optically active hydroxy acids

Journal of the American Chemical Society ◽

10.1021/ja00708a017 ◽

1970 ◽

Vol 92 (5) ◽

pp. 1211-1214 ◽

Cited By ~ 12

Author(s):

Leonard I. Katzin ◽

Elsie. Gulyas

Keyword(s):

Optically Active ◽

Spectral Studies ◽

Hydroxy Acids ◽

Circular Dichroic

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Studies on Optically Active Amino Acids. V. Synthesis of Optically Active α-Aminoalcohols by the Reduction of α-Amino Acid Esters with Sodium Borohydride

Chemical and Pharmaceutical Bulletin ◽

10.1248/cpb.13.995 ◽

1965 ◽

Vol 13 (8) ◽

pp. 995-1000 ◽

Cited By ~ 67

Author(s):

Hedeo Seki ◽

Kenji Koga ◽

Hisayuki Matsuo ◽

Sadao Ohki ◽

Ichiro Matsuo ◽

...

Keyword(s):

Amino Acids ◽

Amino Acid ◽

Sodium Borohydride ◽

Optically Active ◽

Amino Acid Esters ◽

Acid Esters

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Chemical Relationships of Sugars, Optically Active Amino Acids , Hydroxy Acids, and Halogen Acids

Synthetic Organic Chemistry in the Study of Odorous Compounds ◽

10.7312/boge93008-008 ◽

1927 ◽

pp. 49-76

Keyword(s):

Amino Acids ◽

Optically Active ◽

Hydroxy Acids

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Applications of stereoselectivity of enzymes: Synthesis of optically active amino acids and α-hydroxy acids, and stereospecific isotope-labeling of amino acids, amines and coenzymes

Bioproducts - Advances in Biochemical Engineering/Biotechnology ◽

10.1007/bfb0002454 ◽

2005 ◽

pp. 95-130 ◽

Cited By ~ 3

Author(s):

Kazuo Yonaha ◽

Kenji Soda

Keyword(s):

Amino Acids ◽

Isotope Labeling ◽

Optically Active ◽

Hydroxy Acids

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Enantioselective Reduction of Ketones with Sodium Borohydride, Catalyzed by Optically Active(β-Oxoaldiminato)cobalt(II) Complexes

Angewandte Chemie International Edition in English ◽

10.1002/anie.199521451 ◽

1995 ◽

Vol 34 (19) ◽

pp. 2145-2147 ◽

Cited By ~ 106

Author(s):

Takushi Nagata ◽

Kiyotaka Yorozu ◽

Tohru Yamada ◽

Teruaki Mukaiyama

Keyword(s):

Sodium Borohydride ◽

Optically Active ◽

Enantioselective Reduction ◽

Reduction Of Ketones

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CCXVI.—Experiments on the Walden inversion. Part VII. Action of phosphorus pentachloride and of thionyl chloride on optically active hydroxy-acids and esters

Journal of the Chemical Society Transactions ◽

10.1039/ct9119901910 ◽

1911 ◽

Vol 99 (0) ◽

pp. 1910-1926 ◽

Cited By ~ 11

Author(s):

Alex McKenzie ◽

Fred Barrow

Keyword(s):

Thionyl Chloride ◽

Phosphorus Pentachloride ◽

Optically Active ◽

Hydroxy Acids

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ChemInform Abstract: ASYMMETRIC HALOLACTONIZATION REACTION. I. ASYMMETRIC SYNTHESIS OF OPTICALLY ACTIVE α,α-DISUBSTITUTED-α-HYDROXY ACIDS FROM α,β-UNSATURATED ACIDS BY THE NOVEL USE OF HALOLACTONIZATION REACTION

Chemischer Informationsdienst ◽

10.1002/chin.198006173 ◽

1980 ◽

Vol 11 (6) ◽

Author(s):

S-S. JEW ◽

S. TERASHIMA ◽

K. KOGA

Keyword(s):

Asymmetric Synthesis ◽

Optically Active ◽

The Novel ◽

Hydroxy Acids

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Asymmetric synthesis of optically active threo- and erythro-pyrrolidinylbenzyl alcohol by the highly stereospecific arylation of (S)-proline and the subsequent highly diastereoselective reduction of the α-amino ketone

Journal of the Chemical Society Perkin Transactions 1 ◽

10.1039/p19870001465 ◽

1987 ◽

pp. 1465-1471 ◽

Cited By ~ 31

Author(s):

Atsuhiro Ookawa ◽

Kenso Soai

Keyword(s):

Asymmetric Synthesis ◽

Optically Active ◽

Amino Ketone ◽

Diastereoselective Reduction

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