4.8 Article

Intramolecular [3+2] Cyclocondensations of Alkenes with Indolidenes and Indolidenium Cations

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JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
卷 136, 期 43, 页码 15138-15141

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AMER CHEMICAL SOC
DOI: 10.1021/ja508421e

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  1. Chemical Synthesis Division of the National Science Foundation [CHE0956458]

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C(2)-C(3) cyclopentannelated indole constructs are prepared by either (a) a cyclization cascade of an alkenyl sulfide tethered to a 2-azido-1-allenylbenzene core or (b) cationic cyclization of a tethered alkenyl sulfide with a putative 2-indolidenium cation. In both cases, issues of C-C versus C-N bond formation emerge, and the results indicate that the former is favored.

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