Please use this identifier to cite or link to this item: http://nopr.niscair.res.in/handle/123456789/45934
Title: Enantiospecific syntheses of oxacyclodecanes from carvone via mild Lewis acid mediated etherifcation
Authors: Srikrishna, Adusumilli
Satyanarayana, Gedu
Keywords: (R)-Carvone;Terpenes;Cyclic ethers;Lewis acid;Etherification
Issue Date: Mar-2019
Publisher: NISCAIR-CSIR, India
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.
Page(s): 353-361
URI: http://nopr.niscair.res.in/handle/123456789/45934
ISSN: 0975-0983(Online); 0376-4699(Print)
Appears in Collections:IJC-B Vol.58B(03) [March 2019]

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