Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/53372
Title: Synthesis of cage heterocycles containing tetrahydrofuran and pyran ring system via Grignard addition and ring-closing metathesis
Authors: Kotha, Sambasivarao
Cheekatla, Subba Rao
Keywords: Cage heterocycles;Tetrahydrofuran ring system;Grignard addition;Ring-closing metathesis (RCM);Cage hydroxyethers;Transannular cyclization
Issue Date: Jan-2020
Publisher: NISCAIR-CSIR, India
Abstract: Several cage compounds containing tetrahydrofuran and pyran rings have been reported by using the Grignard addition and ring-closing metathesis as key steps. Cage hemiketal derivatives have been generated due to the proximity of two carbonyl groups in cage dione. These cage heterocycles have been derived from readily available starting materials such as 1,4-hydroquinone and dicyclopentadiene.
Page(s): 75-84
ISSN: 0975-0983(Online); 0376-4699(Print)
Appears in Collections:IJC-B Vol.59B(01) [January 2020]

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