ChemInform Abstract: STERICALLY CONTROLLED SYNTHESIS OF OPTICALLY ACTIVE ORGANIC COMPOUNDS. XXIII. SYMMETRIC SYNTHESIS OF ALANINE BY ALKYLATION OF OPTICALLY ACTI E N-ALKYL-N-FORMYLAMINOACETONITRILES

K. HARADA; M. TAMURA; S. SUZUKI

doi:10.1002/chin.197843073

ChemInform Abstract: STERICALLY CONTROLLED SYNTHESIS OF OPTICALLY ACTIVE ORGANIC COMPOUNDS. XXIII. SYMMETRIC SYNTHESIS OF ALANINE BY ALKYLATION OF OPTICALLY ACTI E N-ALKYL-N-FORMYLAMINOACETONITRILES

Chemischer Informationsdienst ◽

10.1002/chin.197843073 ◽

1978 ◽

Vol 9 (43) ◽

Author(s):

K. HARADA ◽

M. TAMURA ◽

S. SUZUKI

Keyword(s):

Organic Compounds ◽

Optically Active ◽

Controlled Synthesis

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ChemInform Abstract: STERICALLY CONTROLLED SYNTHESIS OF OPTICALLY ACTIVE ORGANIC COMPOUNDS. XXX. ASYMMETRIC SYNTHESIS OF ASPARTIC ACID BY HYDROGENATION OF AN OPTICALLY ACTIVE 1,4-OXAZINE DERIVATIVE

Chemischer Informationsdienst ◽

10.1002/chin.198021075 ◽

1980 ◽

Vol 11 (21) ◽

Author(s):

M. TAMURA ◽

K. HARADA

Keyword(s):

Asymmetric Synthesis ◽

Aspartic Acid ◽

Organic Compounds ◽

Optically Active ◽

Controlled Synthesis ◽

Oxazine Derivative

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ChemInform Abstract: STERICALLY CONTROLLED SYNTHESIS OF OPTICALLY ACTIVE ORGANIC COMPOUNDS. XXXI. ASYMMETRIC HYDROGENATION OF CHIRAL PYRUVAMIDES

Chemischer Informationsdienst ◽

10.1002/chin.198122111 ◽

1981 ◽

Vol 12 (22) ◽

Author(s):

K. HARADA ◽

T. MUNEGUMI ◽

S. NOMOTO

Keyword(s):

Organic Compounds ◽

Asymmetric Hydrogenation ◽

Optically Active ◽

Controlled Synthesis

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ChemInform Abstract: STERICALLY CONTROLLED SYNTHESIS OF OPTICALLY ACTIVE ORGANIC COMPOUNDS. XXVII. SYMMETRIC SYNTHESIS OF N-SUBSTITUTED DIMETHYLAZIRIDINE-2,3-DICARBOXYLATE AND ND THE FORMATION OF OPTICALLY ACTIVE ASPARTIC ACID

Chemischer Informationsdienst ◽

10.1002/chin.197910206 ◽

1979 ◽

Vol 10 (10) ◽

Author(s):

K. HARADA ◽

I. NAKAMURA

Keyword(s):

Aspartic Acid ◽

Organic Compounds ◽

Optically Active ◽

Controlled Synthesis

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Sterically controlled synthesis of optically active organic compounds. V. Sterically controlled synthesis of optically active .alpha.-amino acids from .alpha.-oxo acids by reductive amination

The Journal of Organic Chemistry ◽

10.1021/jo01281a020 ◽

1967 ◽

Vol 32 (6) ◽

pp. 1794-1800 ◽

Cited By ~ 59

Author(s):

Kaoru Harada ◽

Kazuo Matsumoto

Keyword(s):

Amino Acids ◽

Organic Compounds ◽

Reductive Amination ◽

Optically Active ◽

Controlled Synthesis

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Sterically controlled synthesis of optically active organic compounds. VII. Synthesis of optically active alanine from oxalacetic acid by asymmetric reductive amination

The Journal of Organic Chemistry ◽

10.1021/jo01276a050 ◽

1968 ◽

Vol 33 (12) ◽

pp. 4526-4528 ◽

Cited By ~ 11

Author(s):

Kazuo Matsumoto ◽

Kaoru Harada

Keyword(s):

Organic Compounds ◽

Reductive Amination ◽

Optically Active ◽

Controlled Synthesis ◽

Oxalacetic Acid

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Sterically controlled synthesis of optically active organic compounds. VI. Solvent effect in a sterically controlled synthesis of optically active .alpha.-amino acids from .alpha.-oxo acids by reductive amination

The Journal of Organic Chemistry ◽

10.1021/jo01276a036 ◽

1968 ◽

Vol 33 (12) ◽

pp. 4467-4470 ◽

Cited By ~ 29

Author(s):

Kaoru Harada ◽

Kazuo Matsumoto

Keyword(s):

Amino Acids ◽

Solvent Effect ◽

Organic Compounds ◽

Reductive Amination ◽

Optically Active ◽

Controlled Synthesis

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Sterically Controlled Syntheses of Optically Active Organic Compounds. XX. Synthesis of Optically Active Alanine from α-Bromopropionamides

Bulletin of the Chemical Society of Japan ◽

10.1246/bcsj.46.1869 ◽

1973 ◽

Vol 46 (6) ◽

pp. 1869-1872 ◽

Cited By ~ 6

Author(s):

Tadashi Okawara ◽

Kaoru Harada

Keyword(s):

Organic Compounds ◽

Optically Active

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Controlled racemization of optically active organic compounds: Prospects for asymmetric transformation

Tetrahedron ◽

10.1016/s0040-4020(97)00324-4 ◽

1997 ◽

Vol 53 (28) ◽

pp. 9417-9476 ◽

Cited By ~ 220

Author(s):

Eelco J. Ebbers ◽

Gerry J.A. Ariaans ◽

Joannes P.M. Houbiers ◽

Alle Bruggink ◽

Binne Zwanenburg

Keyword(s):

Organic Compounds ◽

Optically Active ◽

Asymmetric Transformation

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ChemInform Abstract: STERICALLY CONTROLLED SYNTHESES OF OPTICALLY ACTIVE ORGANIC COMPOUNDS PART 21, THE TEMPERATURE DEPENDENCE OF HYDROGENOLYTIC ASYMMETRIC TRANSAMINATION BETWEEN OPTICALLY ACTIVE PHENYLGLYCINE AND ALPHA-KETO ACIDS

Chemischer Informationsdienst ◽

10.1002/chin.197336410 ◽

1973 ◽

Vol 4 (36) ◽

pp. no-no

Author(s):

KAORU HARADA ◽

TAMEO IWASAKI ◽

TADASHI OKAWARA

Keyword(s):

Temperature Dependence ◽

Organic Compounds ◽

Optically Active ◽

Keto Acids

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XII.—The rotatory dispersive power of organic compounds. Part V. A comparison of the optical and magnetic rotatory dispersions in some optically active liquids

Journal of the Chemical Society Transactions ◽

10.1039/ct9140500094 ◽

1914 ◽

Vol 105 (0) ◽

pp. 94-102 ◽

Cited By ~ 3

Author(s):

Thomas Martin Lowry ◽

Robert Howson Pickard ◽

Joseph Kenyon

Keyword(s):

Organic Compounds ◽

Optically Active ◽

Dispersive Power

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