Synthesis 2016; 48(10): 1561-1567
DOI: 10.1055/s-0035-1561394
paper
© Georg Thieme Verlag Stuttgart · New York

Stereoselective Total Synthesis of Cryptomoscatone F1

Eedubilli Srinivas
a   Natural Products Chemistry Division, CSIR Indian Institute of Chemical Technology, Tarnaka, Hyderabad 500007, TS, India
b   Academy of Scientific and Innovative Research, New Delhi, India
,
Palash Dutta
a   Natural Products Chemistry Division, CSIR Indian Institute of Chemical Technology, Tarnaka, Hyderabad 500007, TS, India
b   Academy of Scientific and Innovative Research, New Delhi, India
,
Bogonda Ganganna
a   Natural Products Chemistry Division, CSIR Indian Institute of Chemical Technology, Tarnaka, Hyderabad 500007, TS, India
b   Academy of Scientific and Innovative Research, New Delhi, India
,
Ahmad Alkhazim Alghamdi
c   Engineer Abdullah Baqshan for Bee Research, King Saudi University, Saudi Arabia   Email: yadavpub@gmail.com
,
Jhillu Singh Yadav*
a   Natural Products Chemistry Division, CSIR Indian Institute of Chemical Technology, Tarnaka, Hyderabad 500007, TS, India
› Author Affiliations
Further Information

Publication History

Received: 23 December 2015

Accepted after revision: 12 February 2016

Publication Date:
07 March 2016 (online)


Abstract

A concise stereoselective total synthesis of cryptomoscatone F1 has been accomplished by utilization of asymmetric acetate aldol reaction, Brown’s asymmetric allylation, and olefin cross-metathesis as key transformations.

Supporting Information

 
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