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Volumn 13, Issue 15, 2002, Pages 1695-1702
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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
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Author keywords
[No Author keywords available]
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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;
ARTICLE;
BACTERIAL CELL;
CONTROLLED STUDY;
ENANTIOSELECTIVITY;
HYDROLYSIS;
NONHUMAN;
PRIORITY JOURNAL;
RHODOCOCCUS;
STEREOISOMERISM;
STRUCTURE ACTIVITY RELATION;
SYNTHESIS;
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EID: 0037077798
PISSN: 09574166
EISSN: None
Source Type: Journal
DOI: 10.1016/S0957-4166(02)00470-6 Document Type: Article |
Times cited : (38)
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References (29)
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