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A simple and practical one-pot, two-directional approach to access olefinic esters through simultaneous breaking and making of olefins using ozonolysis of alkenyl aryl selenides is disclosed. The scope of the method with a variety of examples is demonstrated, and the end products obtained here are useful building blocks. As a direct application of the present method, the macrocyclic core of potent anti-inflammatory natural cyclic peptides, solomonamides, is synthesized.
Breaking and Making of Olefins Simultaneously Using Ozonolysis: Application to the Synthesis of Useful Building Blocks and Macrocyclic Core of Solomonamides
CSIR-National Chemical Laboratory, Division of Organic Chemistry, Dr. Homi Bhabha Road, Pune 411008, India
Org. Lett., 2015, 17 (9), pp 2090–2093
DOI: 10.1021/acs.orglett.5b00637
Publication Date (Web): April 14, 2015
Copyright © 2015 American Chemical Society
*E-mail: ds.reddy@ncl.res.in.
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GENERAL METHOD
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Dr. D. Srinivasa Reddy
Filed under: SPOTLIGHT, SYNTHESIS, Uncategorized Tagged: D. Srinivasa Reddy, NCL, OZONOLYSIS, pune
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