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Literature DB >> 18685773

2,3-Heteroaromatic ring-fused cyclohexanones via heteroaromatic homo-Nazarov cyclization of donor-acceptor substituted cyclopropanes.

Veejendra K Yadav¹, Naganaboina Vijaya Kumar.

Abstract

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

Entities: Chemical Species

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Year: 2008 PMID： 18685773 DOI： 10.1039/b805348k

Source DB: PubMed Journal: Chem Commun (Camb) ISSN： 1359-7345 Impact factor: 6.222

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Cited

2 in total

1. One-Pot Catalytic Asymmetric Synthesis of Tetrahydrocarbazoles.

Authors: Qiong-Jie Liu; Wen-Guang Yan; Lijia Wang; X Peter Zhang; Yong Tang
Journal: Org Lett Date: 2015-08-07 Impact factor: 6.005

2. Diastereoselective ring opening of fully-substituted cyclopropanes via intramolecular Friedel-Crafts alkylation.

Authors: Veeranjaneyulu Lanke; Fa-Guang Zhang; Alexander Kaushansky; Ilan Marek
Journal: Chem Sci Date: 2019-08-27 Impact factor: 9.825

2 in total