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Volumn 13, Issue 15, 2002, Pages 1695-1702

Synthesis of enantiomerically enriched (S)-(+)-2-aryl-4-pentenoic acids and (R)-(-)-2-aryl-4-pentenamides via microbial hydrolysis of nitriles, a chemoenzymatic approach to stereoisomers of α,γ-disubstituted γ-butyrolactones

Author keywords

[No Author keywords available]

Indexed keywords

2 (2 METHYLPHENYL) 4 PENTENAMIDE; 2 (2 METHYLPHENYL) 4 PENTENENITRILE; 2 (2 METHYLPHENYL) 4 PENTENOIC ACID; 2 (3 METHYLPHENYL) 4 IODOMETHYL GAMMA BUTYROLACTONE; 2 (3 METHYLPHENYL) 4 PENTENAMIDE; 2 (3 METHYLPHENYL) 4 PENTENENITRILE; 2 (3 METHYLPHENYL) 4 PENTENOIC ACID; 2 (4 CHLOROPHENYL) 4 PENTENAMIDE; 2 (4 CHLOROPHENYL) 4 PENTENENITRILE; 2 (4 CHLOROPHENYL) 4 PENTENOIC ACID; 2 (4 FLUOROPHENYL) 4 PENTENAMIDE; 2 (4 FLUOROPHENYL) 4 PENTENENITRILE; 2 (4 FLUOROPHENYL) 4 PENTENOIC ACID; 2 (4 METHOXYPHENYL) 4 PENTENAMIDE; 2 (4 METHOXYPHENYL) 4 PENTENENITRILE; 2 (4 METHOXYPHENYL) 4 PENTENOIC ACID; 2 (4 METHYLPHENYL) 4 PENTENENITRILE; 2 PHENYL 4 PENTENAMIDE; 2 PHENYL 4 PENTENENITRILE; 2 PHENYL 4 PENTENOIC ACID; 3 (3 METHYLPHENYL) 5 IODOMETHYL GAMMA BUTYROLACTONE; 3 (4 METHYLPHENYL) 5 IODOMETHYL GAMMA BUTYROLACTONE; ACID; AMIDASE; AMIDE; GAMMA BUTYROLACTONE DERIVATIVE; NITRILE; NITRILE HYDRATASE; UNCLASSIFIED DRUG;

EID: 0037077798     PISSN: 09574166     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0957-4166(02)00470-6     Document Type: Article
Times cited : (38)

References (29)
  • 28
    • 4243523714 scopus 로고
    • Makosza, M.; Serafin, B. Rocz. Chem. 1965, 39, 1805-1810; Chem. Abstr. 1966, 64, 17476a.
    • (1966) Chem. Abstr. , vol.64


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.