NHC-catalysed annulation of enals to tethered dienones: efficient synthesis of bicyclic dienesElectronic supplementary information (ESI) available: Further experimental details and NMR spectra. CCDC reference numbers 777238. For ESI and crystallographic data in CIF or other electronic format see DOI: 10.1039/c0ob00180e

Homoenolates generated from α,β-unsaturated aldehydes using NHC catalysis underwent facile addition to dibenzylidene cyclohexanone to afford bicyclic cyclopentenes as single diastereomers. Homoenolates generated from α,β-unsaturated aldehydes using NHC catalysis underwent facile addition to dibenzyl...

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Main Authors: Nair, Vijay, Vellalath, Sreekumar, Babu, Beneesh P, Varghese, Vimal, Paul, Rony Rajan, Suresh, Eringathodi
Format: Article
Language:English
Online Access:Get full text
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Summary:Homoenolates generated from α,β-unsaturated aldehydes using NHC catalysis underwent facile addition to dibenzylidene cyclohexanone to afford bicyclic cyclopentenes as single diastereomers. Homoenolates generated from α,β-unsaturated aldehydes using NHC catalysis underwent facile addition to dibenzylidene cyclohexanone to afford bicyclic cyclopentenes as single diastereomers.
ISSN:1477-0520
1477-0539
DOI:10.1039/c0ob00180e