Stereoselective syntheses of trans- and cis-cinnamic acid esters from the phenylalanine derivatives.

Tetrahedron Letters

Volumn 14, Issue 43, 1973, Pages 4267-4270

  Takamura, Norio ^a   Mizoguchi, Tomishige ^a   Yamada, Shun ichi ^b  

^a MITSUBISHI TANABE PHARMA CORPORATION   (Japan)

^b UNIVERSITY OF TOKYO   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

CINNAMIC ACID DERIVATIVE; CINNAMIC ACID METHYL ESTER; UNCLASSIFIED DRUG;

DRUG ANALYSIS; DRUG STRUCTURE; DRUG SYNTHESIS; IN VITRO STUDY; METHODOLOGY; STEREOCHEMISTRY; THEORETICAL STUDY; THIN LAYER CHROMATOGRAPHY;

EID: 0015838053     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(01)87166-5     Document Type: Article

References (10)

1. Stereochemical Studies. XIV. Studies on the Neighboring Aryl Group Participation in Nitrous Acid Deaminations of L-Phenylalanine Ethyl Ester and Its p-Nitro and p-Methoxy Derivatives
2. Stereochemical Studies. XV. Neighboring Aryl Group Participation in Nitrous Acid Deaminations of L-Phenylalanine and Its p-Nitro and p-Methoxy Derivatives. Conversion of L-Phenylalanine to naturally Occurring S-Tropic Acid