Redox neutral [4+2] benzannulation of dienals and tertiary enaminones for benzaldehyde synthesis

Chem. Commun., 2018, Advance Article DOI: 10.1039/C8CC03514H, CommunicationLu Yang, Li Wei, Jie-Ping Wan The [4+2] benzannulation reactions between tertiary enaminones and dienals have been developed for the synthesis of polyfunctionalized benzaldehydes, providing a new access to benzaldehydes alongside the classical formylation strategy. To cite this article before page numbers are assigned, use the DOI form of citation above. The content of this RSS Feed (c) The Royal Society of Chemistry

Source: RSC - Chem. Commun. latest articles - June 19, 2018 Category: Chemistry Authors: Lu Yang Source Type: research