Selective syntheses of diversely substituted 2-hydroxy-4′-hydroxybenzophenones through [4 + 2] or [3 + 3] annulation of penta-3,4-dien-2-ones with 3-formylchromones

Literature Information

Publication Date 2017-06-29
DOI 10.1039/C7QO00366H
Impact Factor 5.281
Authors

Xiaonan Shi, Yan He, Xinying Zhang, Xuesen Fan


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Abstract

A selective synthesis of 2-hydroxy-4′-hydroxybenzophenones or their 3′-acylated counterparts through the cascade reactions of 3-formylchromones with diversely substituted penta-3,4-dien-2-ones is presented. Mechanistically, the formation of the title compounds involves either an unprecedented [4 + 2] annulation or a well defined [3 + 3] cyclization depending on the substitution patterns of the penta-3,4-dien-2-one substrates.

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Contents

Front/Back Matter

DOI: 10.1039/C0CP90048F

Back matter

Front/Back Matter

DOI: 10.1039/C0CP90030C

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