𝔖 Bobbio Scriptorium
✦   LIBER   ✦

A biogenetic-type asymmetric synthesis of natural (+)-maritidine from L-tyrosine

✍ Scribed by Shun-ichi Yamada; Kiyoshi Tomioka; Kenji Koga


Book ID
104212912
Publisher
Elsevier Science
Year
1976
Tongue
French
Weight
202 KB
Volume
17
Category
Article
ISSN
0040-4039

No coin nor oath required. For personal study only.


πŸ“œ SIMILAR VOLUMES


Total synthesis of (–)-MY 336a from L-ty
✍ Xiang Wei Liao; Wen Fang Dong; Wei Liu; Bao He Guan; Zhan Zhu Liu πŸ“‚ Article πŸ“… 2009 πŸ› Journal of Heterocyclic Chemistry 🌐 English βš– 73 KB

## Abstract magnified image Using L‐tyrosine as a chiral starting material, we developed an efficient synthetic route to (–)‐MY 336a. A key step in the sequence is a highly regio‐ and diastereoselective intermolecular Pictet‐Spengler cyclization reaction between amino alcohol and benzyloxyacetalde

A biogenetic-type synthesis of (Β±)-aplys
✍ Haruki Niwa; Shigeru Ieda; Hideaki Inagaki; Kiyoyuki Yamada πŸ“‚ Article πŸ“… 1990 πŸ› Elsevier Science 🌐 French βš– 151 KB

f)-Aplysiadiol (1). a brominated diterpene having a ram, prenylated eudesmane skeleton was synthesized starting with (\*)-hedycaryol(2) in a biogenetic manner. Aplysiadiol(1) isolated ftom the Japanese marine mollusc ApZysti kurodai is a brominated diterpene having a rate, prenylated eudesmane skel