ENANTIOSELECTIVE SYNTHESIS OF 20(S)-CAMPTOTHECIN USING SHARPLESS CATALYTIC ASYMMETRIC DIHYDROXYLATION

Authors
JEW SS OK KD KIM HJ KIM MG KIM JM HAH JM CHO YS
Citation
Ss. Jew et al., ENANTIOSELECTIVE SYNTHESIS OF 20(S)-CAMPTOTHECIN USING SHARPLESS CATALYTIC ASYMMETRIC DIHYDROXYLATION, Tetrahedron : asymmetry, 6(6), 1995, pp. 1245-1248
Citations number
29
Categorie Soggetti
Chemistry Inorganic & Nuclear","Chemistry Inorganic & Nuclear","Chemistry Physical
Journal title
Tetrahedron : asymmetry → ACNP
ISSN journal
09574166
Volume
6
Issue
6
Year of publication
1995
Pages
1245 - 1248
Database
ISI
SICI code
0957-4166(1995)6:6<1245:ESO2US>2.0.ZU;2-Q
Abstract
The homochiral key intermediate 2 of 20(S)-camptothecin was prepared e nantioselectively by using catalytic asymmetric dihydroxylation as the key reaction.