Synthesis and Structure of 3,4-Dihydro-4-phenyl-1,5-benzodioxepin-2-ones
摘要:
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.
Synthesis and Structure of 3,4-Dihydro-4-phenyl-1,5-benzodioxepin-2-ones
作者:Aifheli C. Gelebe、Perry T. Kaye、J. Richard Liddell
DOI:10.1080/00397919108021584
日期:1991.12
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.
Gelebe, Aifheli C.; Kaye, Perry T., Journal of Chemical Research - Part S, 1996, # 1, p. 26 - 27