Synthesis of Condensed Pyrroloindoles via Pd-Catalyzed Intramolecular C-H Bond Functionalization of Pyrroles

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A new strategy for the synthesis of condensed hetero- or carbocycles such as pyrroloindoles or fluorenes has been developed that involves the Pd-catalyzed cyclization of readily available N-(2-halobenzyl)pyrroles or their phenyl derivatives. The reaction is proposed to proceed via oxidative addition of benzylic halides to Pd(0) followed by base-assisted C-H bond activation. A broad range of condensed cyclic products could be obtained in good to excellent yields under mild conditions.
Publisher
AMER CHEMICAL SOC
Issue Date
2008-12
Language
English
Article Type
Article
Keywords

N-FUSED HETEROCYCLES; DIRECT ARYLATION; ARYL CHLORIDES; ACTIVATION; INDOLES; REGIOSELECTIVITY; HYDROARYLATION; ALKENYLATION; DERIVATIVES; MECHANISM

Citation

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, v.130, no.48, pp.16158 - 16158

ISSN
0002-7863
DOI
10.1021/ja806897h
URI
http://hdl.handle.net/10203/88633
Appears in Collection
CH-Journal Papers(저널논문)
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