Switching enantiofacial selectivities using one chiral source: Catalytic enantioselective synthesis of the key intermediate for (20S)-camptothecin family by (S)-selective cyanosilylation of ketones [7]

Journal of the American Chemical Society

Volumn 123, Issue 40, 2001, Pages 9908-9909

  Yabu, K ^a   Masumoto, S ^a   Yamasaki, S ^a   Hamashima, Y ^a   Kanai, M ^a   Du, W ^a   Curran, D P ^a   Shibasaki, M ^a  

^a UNIVERSITY OF TOKYO   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

CAMPTOTHECIN DERIVATIVE; KETONE;

CATALYSIS; CHEMICAL MODIFICATION; CHIRALITY; DRUG SYNTHESIS; ENANTIOMER; LETTER; STEREOCHEMISTRY;

CAMPTOTHECIN; CYANIDES; GLUCOSE; STEREOISOMERISM; TRIMETHYLSILYL COMPOUNDS;

EID: 0035840992     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja016682n     Document Type: Letter

References (22)