๐”– Bobbio Scriptorium
โœฆ   LIBER   โœฆ

Synthetic studies of trichothecenes, an enantioselective synthesis of a C-ring precursor of anguidine

โœ Scribed by Dee W. Brooks; Paul G. Grothaus; James T. Palmer


Book ID
104221968
Publisher
Elsevier Science
Year
1982
Tongue
French
Weight
254 KB
Volume
23
Category
Article
ISSN
0040-4039

No coin nor oath required. For personal study only.


๐Ÿ“œ SIMILAR VOLUMES


Studies on the asymmetric total synthesi
โœ Duy H. Hua; S. Venkataraman ๐Ÿ“‚ Article ๐Ÿ“… 1985 ๐Ÿ› Elsevier Science ๐ŸŒ French โš– 262 KB

A stereoselective construction of the C-ring fragment of trichothecenes from readily available 4-cumyloxy-2-cyclopentenol in 12 steps (24% overall yield) is described. We have recently described an asymmetric synthesis based on the reaction of enones with chiral sulfinylallyl anions.' The utilizatio

A concise enantioselective synthesis of
โœ Olivier Roy; Gerald Pattenden; David C. Pryde; Claire Wilson ๐Ÿ“‚ Article ๐Ÿ“… 2003 ๐Ÿ› Elsevier Science ๐ŸŒ French โš– 154 KB

A concise synthesis of the oxygen substituted ring A compound 2 found in Taxol w 1a and Taxotere w 1b starting from 2,2dimethylcyclohexane-1,3-dione and proceeding via the key intermediates 8 and 11, is described. The absolute configuration of 2 was established from an X-ray crystal structure determ