Synthesis 2015; 47(04): 485-488
DOI: 10.1055/s-0034-1379582
paper
© Georg Thieme Verlag Stuttgart · New York

Synthesis of Yangjinhualine A

Prashant S. Deore
Division of Organic Chemistry, National Chemical Laboratory (CSIR), Pune 411 008, India   Email: np.argade@ncl.res.in
,
Ramesh U. Batwal
Division of Organic Chemistry, National Chemical Laboratory (CSIR), Pune 411 008, India   Email: np.argade@ncl.res.in
,
Narshinha P. Argade*
Division of Organic Chemistry, National Chemical Laboratory (CSIR), Pune 411 008, India   Email: np.argade@ncl.res.in
› Author Affiliations
Further Information

Publication History

Received: 15 August 2014

Accepted after revision: 30 October 2014

Publication Date:
09 December 2014 (online)


Abstract

Selective reduction of 3-(4-hydroxyphenyl)-2-methylmaleic anhydride provides access the corresponding γ-hydroxybutenolide natural product yangjinhualine A.

Supporting Information

 
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