Synthesis and Structure of 3,4-Dihydro-4-phenyl-1,5-benzodioxepin-2-ones

1 December 1991

journal article
research article
Published by Taylor & Francis in Synthetic Communications

Vol. 21 (22) , 2263-2268
https://doi.org/10.1080/00397919108021584

Abstract

Baeyer-Villiger rearrangement of substituted flavanones using MCPBA affords ring-expanded products, shown by NMR spectroscopy to be the corresponding 3,4-dihydro-4-phenyl-1,5-benzodioxepin-2-ones.

Keywords

BENZODIOXEPIN
DIHYDRO
PHENYL
SYNTHESIS AND STRUCTURE

This publication has 1 reference indexed in Scilit:

A FACILE SYNTHESIS OF 3,4-DIHYDRO-1,5-BENZODIOXEPIN-2-ONES
Organic Preparations and Procedures International, 1989