๐”– Bobbio Scriptorium
โœฆ   LIBER   โœฆ

ChemInform Abstract: A Convergent Approach to Cyclopeptide Alkaloids: Total Synthesis of Sanjoinine G1.

โœ Scribed by Taoues Temal-Laib; Jacqueline Chastanet; Jieping Zhu


Publisher
John Wiley and Sons
Year
2010
Weight
25 KB
Volume
33
Category
Article
ISSN
0931-7597

No coin nor oath required. For personal study only.


๐Ÿ“œ SIMILAR VOLUMES


ChemInform Abstract: Total Synthesis of
โœ S. P. EAST; F. SHAO; L. WILLIAMS; M. M. JOULLIE ๐Ÿ“‚ Article ๐Ÿ“… 2010 ๐Ÿ› John Wiley and Sons โš– 34 KB ๐Ÿ‘ 1 views

Total Synthesis of the Cyclopeptide Alkaloid Sanjoinine G1 and Its C-11 Epimer. -An efficient new synthesis (18 steps, 6.6% overall yield) of sanjoinine G1 (VIII) is reported. The key steps in this synthesis are the formation of the alkyl-aryl ether linkage via an S N Ar reaction of amino alcohol (

ChemInform Abstract: An Asymmetric Total
โœ Taoues Laib; Jieping Zhu ๐Ÿ“‚ Article ๐Ÿ“… 2010 ๐Ÿ› John Wiley and Sons โš– 28 KB ๐Ÿ‘ 1 views

An Asymmetric Total Synthesis of Sanjoinine G1. -Key step in the strategy developed is the cyclization of the linear tripeptide (V) to afford the 14-membered ansa cyclophane (VI). -(LAIB, TAOUES; ZHU, JIEPING;