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One-pot tandem approach for the diastereoselective syn-diacetoxylation of cinnamic esters

Chandrappa, S and Narasimhamurthy, KH and Joy, MN and Rangappa, KS (2021) One-pot tandem approach for the diastereoselective syn-diacetoxylation of cinnamic esters. In: Chemical Data Collections, 34 .

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Official URL: https://doi.org/10.1016/j.cdc.2021.100710

Abstract

One pot selective syn diacetoxylation of in situ generated cinnamic esters using PhI(OAc)2/T3P system, started from gem�dibromomethylarenes in the presence malonoate esters/malononitrile. A broad range of substrates including both electron-deficient and electron-donating gem�dibromomethylarenes could be efficiently elaborated by this developed methodology thereby furnishing the desired products in good to excellent yields. © 2021

Item Type: Journal Article
Publication: Chemical Data Collections
Publisher: Elsevier B.V.
Additional Information: The copyright for this article belongs to Elsevier B.V.
Department/Centre: Division of Biological Sciences > Molecular Biophysics Unit
Date Deposited: 27 Aug 2021 09:44
Last Modified: 27 Aug 2021 09:44
URI: http://eprints.iisc.ac.in/id/eprint/69306

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