z-logo
Premium
Stereoselective Synthesis of γ‐Butyrolactones Subunit of Polycavernoside A
Author(s) -
Kadari Sudhakar,
Yerrabelly Hemasri,
Gogula Thirupathi,
Erukala Yadaiah Goud,
Yerrabelly Jayaprakash Rao,
Begari Prem Kumar
Publication year - 2018
Publication title -
journal of heterocyclic chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.321
H-Index - 59
eISSN - 1943-5193
pISSN - 0022-152X
DOI - 10.1002/jhet.3240
Subject(s) - chemistry , stereoselectivity , ring closing metathesis , yield (engineering) , stereochemistry , protein subunit , metathesis , sharpless epoxidation , combinatorial chemistry , organic chemistry , catalysis , polymerization , biochemistry , polymer , metallurgy , materials science , gene
An efficient and versatile linear synthesis of γ‐butyrolactone subunit of polycavernolide A has been reported in 14.2% overall yield with 10 linear steps by employing Sharpless asymmetric epoxidation, ring‐closing metathesis, and diastereoface selective hydrogenation.

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here