𝔖 Bobbio Scriptorium
✦   LIBER   ✦

A practical enantioselective synthesis of the cigarette beetle sex pheromone serricornin

✍ Scribed by Philip C.-M. Chan; J.Michael Chong; Karim Kousha


Publisher
Elsevier Science
Year
1994
Tongue
French
Weight
704 KB
Volume
50
Category
Article
ISSN
0040-4020

No coin nor oath required. For personal study only.

✦ Synopsis


4RS,6S,7S)-7-hydroxy-4.6-dimethyl-3-nonanone (serricomin and its C4epimez) may be prepared from oxazolidinone 5 in 8 steps with an overall yield of 33%.


πŸ“œ SIMILAR VOLUMES


Absolute stereochemistry of serricornin,
✍ Masataka Mori; Tatsuji Chuman; Masahiro Kohno; Kunio Kato; Masao Noguchi; Hiroko πŸ“‚ Article πŸ“… 1982 πŸ› Elsevier Science 🌐 French βš– 197 KB

## Sumnary: The absolute stereochemistry of serricornin was determined to be (4S,6S,7S) by the synthesis of its (4S,6R,7R)-isomer using a carbohydrate synthon. ## Serricornin (la)[ 4,6-dimethyl-7-hydroxynonan-3-one ] is the sex pheromone of the female -