Stereochemical studies. 44. Exploitation of the new synthetic scheme for chiral additives usable in asymmetric syntheses. Novel syntheses of optically active .GAMMA.-amino acids and pyrrolidines from L-.ALPHA.-amino acids.

CHUNGCHYI TSENG; SHIRO TERASHIMA; SHUNICHI YAMADA

doi:10.1248/cpb.25.29

Stereochemical studies. 44. Exploitation of the new synthetic scheme for chiral additives usable in asymmetric syntheses. Novel syntheses of optically active .GAMMA.-amino acids and pyrrolidines from L-.ALPHA.-amino acids.

Chemical and Pharmaceutical Bulletin ◽

10.1248/cpb.25.29 ◽

1977 ◽

Vol 25 (1) ◽

pp. 29-40 ◽

Cited By ~ 27

Author(s):

CHUNGCHYI TSENG ◽

SHIRO TERASHIMA ◽

SHUNICHI YAMADA

Keyword(s):

Amino Acids ◽

Optically Active ◽

Asymmetric Syntheses

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Sterically controlled syntheses of optically active organic compounds. XVIII. Asymmetric syntheses of optically active amino acids by addition of hydrogen cyanide to Schiff bases

The Journal of Organic Chemistry ◽

10.1021/jo00944a020 ◽

1973 ◽

Vol 38 (4) ◽

pp. 707-710 ◽

Cited By ~ 41

Author(s):

Kaoru Harada ◽

Tadashi Okawara

Keyword(s):

Amino Acids ◽

Organic Compounds ◽

Schiff Bases ◽

Hydrogen Cyanide ◽

Optically Active ◽

Asymmetric Syntheses

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ChemInform Abstract: Asymmetric Syntheses of Optically Active α,β-Disubstituted . beta.-Amino Acids.

ChemInform ◽

10.1002/chin.199351059 ◽

2010 ◽

Vol 24 (51) ◽

pp. no-no

Author(s):

K. BURGESS ◽

L. T. LIU ◽

B. PAL

Keyword(s):

Amino Acids ◽

Optically Active ◽

Asymmetric Syntheses

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ChemInform Abstract: STERICALLY CONTROLLED SYNTHESES OF OPTICALLY ACTIVE ORGANIC COMPOUNDS PART 19, ASYMMETRIC SYNTHESES OF AMINO ACIDS BY THE STRECKER REACTION

Chemischer Informationsdienst ◽

10.1002/chin.197336407 ◽

1973 ◽

Vol 4 (36) ◽

pp. no-no

Author(s):

KAORU HARADA ◽

TADASHI OKAWARA ◽

KAZUO MATSUMOTO

Keyword(s):

Amino Acids ◽

Organic Compounds ◽

Optically Active ◽

Asymmetric Syntheses ◽

Strecker Reaction

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ChemInform Abstract: STEREOCHEMICAL STUDIES. XLIV. EXPLOITATION OF THE NEW SYNTHETIC SCHEME FOR CHIRAL ADDITIVES USABLE IN ASYMMETRIC SYNTHESES. NOVEL SYNTHESES OF OPTICALLY ACTIVE Γ-AMINO ACIDS AND PYRROLIDINES FROM L-α-AMINO ACIDS

Chemischer Informationsdienst ◽

10.1002/chin.197723087 ◽

1977 ◽

Vol 8 (23) ◽

pp. no-no

Author(s):

C. C. TSENG ◽

S. TERASHIMA ◽

S. YAMADA

Keyword(s):

Amino Acids ◽

Optically Active ◽

Asymmetric Syntheses

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Sterically Controlled Syntheses of Optically Active Organic Compounds. XVII. Asymmetric Syntheses of Amino Acids by Addition of Benzoyl Cyanide to the Azomethine Compounds

Bulletin of the Chemical Society of Japan ◽

10.1246/bcsj.46.191 ◽

1973 ◽

Vol 46 (1) ◽

pp. 191-193 ◽

Cited By ~ 11

Author(s):

Kaoru Harada ◽

Tadashi Okawara

Keyword(s):

Amino Acids ◽

Organic Compounds ◽

Optically Active ◽

Asymmetric Syntheses ◽

Benzoyl Cyanide ◽

Azomethine Compounds

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Asymmetric syntheses of optically active .alpha.,.beta.-disubstituted .beta.-amino acids

The Journal of Organic Chemistry ◽

10.1021/jo00069a052 ◽

1993 ◽

Vol 58 (17) ◽

pp. 4758-4763 ◽

Cited By ~ 81

Author(s):

Kevin Burgess ◽

Lee T. Liu ◽

Biman Pal

Keyword(s):

Amino Acids ◽

Optically Active ◽

Asymmetric Syntheses ◽

Alpha Beta

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Sterically Controlled Syntheses of Optically Active Organic Compounds. XIX. Asymmetric Syntheses of Amino Acids by the Strecker Reaction

Bulletin of the Chemical Society of Japan ◽

10.1246/bcsj.46.1865 ◽

1973 ◽

Vol 46 (6) ◽

pp. 1865-1868 ◽

Cited By ~ 16

Author(s):

Kaoru Harada ◽

Tadashi Okawara ◽

Kazuo Matsumoto

Keyword(s):

Amino Acids ◽

Organic Compounds ◽

Optically Active ◽

Asymmetric Syntheses ◽

Strecker Reaction

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Asymmetric syntheses of optically active α-amino acids by hydrocyanic acid addition to the optically active Schiff base

Canadian Journal of Chemistry ◽

10.1139/v70-310 ◽

1970 ◽

Vol 48 (12) ◽

pp. 1881-1884 ◽

Cited By ~ 37

Author(s):

Mahendra S. Patel ◽

Michael Worsley

Keyword(s):

Amino Acids ◽

Schiff Base ◽

Optical Purity ◽

Optically Active ◽

Hydrocyanic Acid ◽

Asymmetric Syntheses ◽

Acid Addition

The syntheses of L(+) and D(−) enantiomers of α-amino acids, norvaline, norleucine, and leucine, as their hydrochloride salts have been achieved in almost 100% optical purity and 40–60% overall yield.

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ChemInform Abstract: TRANSITION METAL CATALYZED ASYMMETRIC ORGANIC SYNTHESES VIA POLYMER-ATTACHED OPTICALLY ACTIVE PHOSPHINE LIGANDS. SYNTHESIS OF R AMINO ACIDS AND HYDRATROPIC ACID BY HYDROGENATION

Chemischer Informationsdienst ◽

10.1002/chin.197818313 ◽

1978 ◽

Vol 9 (18) ◽

Author(s):

N. TAKAISHI ◽

H. IMAI ◽

C. A. BERTELO ◽

J. K. STILLE

Keyword(s):

Amino Acids ◽

Transition Metal ◽

Optically Active ◽

Phosphine Ligands ◽

Organic Syntheses ◽

Transition Metal Catalyzed ◽

Metal Catalyzed

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ChemInform Abstract: New Asymmetric Syntheses of β-Hydroxy-α-amino Acids and Analogues. Components of Biologically Active Cyclopeptides

ChemInform ◽

10.1002/chin.199643266 ◽

2010 ◽

Vol 27 (43) ◽

pp. no-no

Author(s):

J.-P. GENET

Keyword(s):

Amino Acids ◽

Biologically Active ◽

Asymmetric Syntheses

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