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Issue 32, 2008
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2,3-Heteroaromatic ring-fused cyclohexanonesvia heteroaromatic homo-Nazarov cyclization of donor–acceptor substituted cyclopropanes

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Abstract

Heteroaryl 2-silylmethyl-substituted cyclopropylketones rearrange under Lewis acid conditions via heteroaromatic homo-Nazarov cyclization to form 2,3-heteroaromatic ring fused 4-t-butyldiphenylsilylmethyl-substituted cyclohexanones.

Graphical abstract: 2,3-Heteroaromatic ring-fused cyclohexanonesvia heteroaromatic homo-Nazarov cyclization of donor–acceptor substituted cyclopropanes

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Article information


Submitted
31 Mar 2008
Accepted
07 May 2008
First published
18 Jun 2008

Chem. Commun., 2008, 3774-3776
Article type
Communication

2,3-Heteroaromatic ring-fused cyclohexanonesvia heteroaromatic homo-Nazarov cyclization of donor–acceptor substituted cyclopropanes

V. K. Yadav and N. V. Kumar, Chem. Commun., 2008, 3774
DOI: 10.1039/B805348K

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