Issue 1, 2017

Deconjugative alkylation/Heck reaction as a simple platform for dihydronaphthalene synthesis

Abstract

A simple platform for carbocycle synthesis by Knoevenagel adduct deconjugative alkylation/Heck reaction is described. Deconjugative alkylation of Knoevenagels adducts is two-fold synthetically enabling because C–C bond formation is (1) operationally simple due to the ease of Knoevenagel adduct carbanion generation and (2) results in alkene migration, which poises the substrate for cyclization. Furthermore, the gem-dinitrile moiety serves as a functional group for synthetic manipulation.

Graphical abstract: Deconjugative alkylation/Heck reaction as a simple platform for dihydronaphthalene synthesis

Supplementary files

Article information

Article type
Communication
Submitted
14 Oct 2016
Accepted
10 Nov 2016
First published
14 Nov 2016

Org. Biomol. Chem., 2017,15, 69-75

Deconjugative alkylation/Heck reaction as a simple platform for dihydronaphthalene synthesis

P. V. Navaratne and A. J. Grenning, Org. Biomol. Chem., 2017, 15, 69 DOI: 10.1039/C6OB02250B

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