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Tetrahedron Letters

Volumn 42, Issue 44, 2001, Pages 7867-7871

An enantio- and stereocontrolled route to epopromycin B via cinchona alkaloid-catalyzed Baylis-Hillman reaction

(4) Iwabuchi, Yoshiharu a Sugihara, Tatsuya a Esumi, Tomoyuki a Hatakeyama, Susumi a

a NAGASAKI UNIVERSITY (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

CARBONYL DERIVATIVE; CINCHONA ALKALOID; EPOPROMYCIN B; N 9 FLUOROENYLMETHYLOXYCARBONYL LEUCINAL; STATINE DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; CATALYSIS; CHEMICAL REACTION; CHEMICAL STRUCTURE; DRUG SYNTHESIS; ENANTIOMER; PHARMACOPHORE; REACTION ANALYSIS; STEREOCHEMISTRY;

CINCHONA;

EID: 0035968965 PISSN: 00404039 EISSN: None Source Type: Journal
DOI: 10.1016/S0040-4039(01)01676-8 Document Type: Article

Times cited : (103)

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