A concise synthesis of 3-aroylflavones via Lewis base 9-azajulolidine-catalyzed tandem acyl transfer-cyclization.

A concise synthesis of 3-aroylflavones via Lewis base 9-azajulolidine-catalyzed tandem acyl transfer-cyclization.
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DOI:
10.1039/c2cc37015h
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发表时间:
2012-11
影响因子:
4.9
通讯作者:
Masahito Yoshida;Koya Saito;Yuta Fujino;T. Doi
Masahito Yoshida;Koya Saito;Yuta Fujino;T. Doi
中科院分区:
化学2区
文献类型:
--
作者:
Masahito Yoshida;Koya Saito;Yuta Fujino;T. Doi

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Lewis base-catalyzed tandem acyl transfer-cyclization of acylated o-alkynoylphenols leading to 3-aroylflavones was developed. 9-Azajulolidine smoothly promoted the reaction of the aroyl derivatives at ambient temperature, and the structure-diversed synthesis of 3-aroylflavones with distinct substituents was achieved in moderate to excellent yields.