๐”– Bobbio Scriptorium
โœฆ   LIBER   โœฆ

A stereoselective total synthesis of podocarpic acid

โœ Scribed by Walter L. Meyer; Krishna K. Maheshwari

Publisher
Elsevier Science
Year
1964
Tongue
French
Weight
194 KB
Volume
5
Category
Article
ISSN
0040-4039

No coin nor oath required. For personal study only.

โœฆ Synopsis

One of the foremest problems encountered in synthesis of diterpenoid resin acids is that of stereoselective introduction of methyl and carboxyl substituents at the quaternary k-position in the correct configuration relative to the C-10 angular methyl. Most previous syntheses

๐Ÿ“œ SIMILAR VOLUMES

A novel stereoselective synthesis of the
A novel stereoselective synthesis of the ring AB podocarpate system
โœ Ling Lu; Richard K. Shoemaker; Desmond M.S. Wheeler ๐Ÿ“‚ Article ๐Ÿ“… 1989 ๐Ÿ› Elsevier Science ๐ŸŒ French โš– 209 KB

A new way of stereoselectively synthesizing rings A and B of podocarpate has been developed; the correct stereochemistry at C, is obtained during a cyclization linking Cz to C,. Although members of the family of norditerpenoid dilactones that includes inumakilactones, podolactones, nagilactones, pod