Enantiospecific syntheses of oxacyclodecanes from carvone via mild Lewis acid mediated etherifcation

Adusumilli, Srikrishna and G, Satyanarayana (2019) Enantiospecific syntheses of oxacyclodecanes from carvone via mild Lewis acid mediated etherifcation. Indian Journal of Chemistry : Section B, 58B. pp. 353-361. ISSN 0376-4699

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Abstract

An efficient enantiospecific syntheses of oxatri-/tetra-cyclodecanes have been accomplished starting from (R)-carvone. A mild Lewis acid (BF3×OEt2) mediated intramolecular etherification is used as the key step. Structurally aesthetic tri- and tetracyclic ethers have been synthesized.

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IITH Creators:	IITH Creators ORCiD G, Satyanarayana UNSPECIFIED
Item Type:	Article
Subjects:	Chemistry
Divisions:	Department of Chemistry
Depositing User:	Team Library
Date Deposited:	16 Mar 2019 08:59
Last Modified:	16 Mar 2019 08:59
URI:	http://raiithold.iith.ac.in/id/eprint/4879
Publisher URL:
Related URLs:	Google Scholar

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