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Stereoselective Total Synthesis of Iso‐Cladospolide B and the 12 Membered‐Macrolactone (6 S ,12 R )‐6‐Hydroxy‐12‐methyloxacyclododecane‐2,5‐dione
Author(s) -
Kumar Pendyala Venkata Arun,
Mallula Venkata Satyanarayana,
Radha Krishna Palakodety
Publication year - 2015
Publication title -
helvetica chimica acta
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.74
H-Index - 82
eISSN - 1522-2675
pISSN - 0018-019X
DOI - 10.1002/hlca.201500030
Subject(s) - chemistry , nonane , total synthesis , natural product , stereochemistry , stereoselectivity , diol , organic chemistry , catalysis
Total syntheses of iso‐cladospolide B ( 1 ) and the 12‐membered macrolactone (6 S ,12 R )‐6‐hydroxy‐12‐methyloxacyclododecane‐2,5‐dione ( 2 ), a non‐natural product, were achieved from a common intermediate starting from commercially available 1,9‐nonane diol.
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