A versatile synthetic route to dehydrobenzoannulenes via in situ generation of reactive alkynes

被引:72
作者
Bell, ML
Chiechi, RC
Johnson, CA
Kimball, DB
Matzger, AJ
Wan, WB
Weakley, TJR
Haley, MM [1 ]
机构
[1] Univ Oregon, Dept Chem, Eugene, OR 97403 USA
[2] Univ Oregon, Inst Sci Mat, Eugene, OR 97403 USA
[3] Univ Michigan, Dept Chem, Ann Arbor, MI 48109 USA
关键词
annulenes; aromaticity; macrocycles; alkynes; polyynes;
D O I
10.1016/S0040-4020(01)00229-0
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
This paper outlines the development of a protocol that allows in situ generation of unstable alkynes under Pd-catalyzed cross-coupling conditions. Cu-mediated intramolecular cyclization of the resultant alpha,omega -polyynes provides dehydrobenzoannulenes as singular species, in very good overall yields, and in a variety of topologies that are inaccessible by traditional routes or previously available in low yield only. In addition, we will discuss the solid-state structure and reactivity of these macrocycles, as well as the ability of the planar dehydrobenzoannulenes to support weak induced ring currents. (C) 2001 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:3507 / 3520
页数:14
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