๐”– Bobbio Scriptorium
โœฆ   LIBER   โœฆ

Short and Versatile Route to a Key Intermediate for Lactacystin Synthesis

โœ Scribed by Bulman Page, Philip C.; Hamzah, A. Sazali; Leach, David C.; Allin, Steven M.; Andrews, David M.; Rassias, Gerasimos A.


Book ID
127072061
Publisher
American Chemical Society
Year
2003
Tongue
English
Weight
53 KB
Volume
5
Category
Article
ISSN
1523-7060

No coin nor oath required. For personal study only.


๐Ÿ“œ SIMILAR VOLUMES


A short and efficient enantioselective r
โœ E.J Corey; Paul Da Silva Jardine ๐Ÿ“‚ Article ๐Ÿ“… 1989 ๐Ÿ› Elsevier Science ๐ŸŒ French โš– 285 KB

A simple route for the enanrioselective synthesis of key intermediates (11 and 12) for the total synthesis of forskolin has been developed starting from acid 6 and (S)-alcohol 5. The latter is prepared by enantioselective catalytic CBS reduction of dienone 3, and is converted by an intramolecular Di

Stereocontrolled route to a key intermed
โœ E.J. Corey; Mark G. Bock ๐Ÿ“‚ Article ๐Ÿ“… 1975 ๐Ÿ› Elsevier Science ๐ŸŒ French โš– 210 KB

We have undertaken a synthesis of this substance as part of a broader program in the area of biologically active macrocyclic natural products. One attractive approach to the synthesis of maytansine involves the introduction of chiraltty at carbons 3, 4, 5, 10, and 9 after formation of the macro ring