Total synthesis of the marine natural product (±)-precapnelladiene
作者:Goverdhan Mehta、A. Narayana Murty
DOI:10.1039/c39840001058
日期:——
A stereo-controlled total synthesis of the novel sesquiterpene precapnelladiene (1), isolated from the soft coral Capnella imbricata, is reported; the synthesis unequivocally establishes the stereochemistry of the natural product as (1).
A general stereocontrolled approach to the 5-8 fused ring system. Application to the total synthesis of the marine natural product (.+-.)-precapnelladiene
作者:Goverdhan Mehta、A. Narayana Murthy
DOI:10.1021/jo00389a040
日期:1987.6
Preparation of (<i>R</i>)-(2-Cyclopentenyl)methanol and the First Total Synthesis of (8<i>R</i>,11<i>R</i>)-Precapnelladiene
作者:Koji Maeda、Yoshinobu Inouye
DOI:10.1246/bcsj.67.2880
日期:1994.10
Enantiometrically pure (R)-(2-cyclopentenyl)methanol (2) was prepared from ethyl 2-oxocyclopentanecarboxylate. Coupling of 2 with 4,4-dimethyl-3-phenylthio-2-cyclohexenone gave an enol ether, which...