Journal Article

N-Heterocyclic-Carbene-Catalysed Diastereoselective Vinylogous Mukaiyama/Michael Reaction of 2-(Trimethylsilyloxy)furan and Enones

Asian Journal of Organic Chemistry (2015) 4(12) 1362-1365
DOI: 10.1002/ajoc.201500348
10Citations
Citations of this article
7Readers
Mendeley users who have this article in their library.
Get full text

Abstract

N-heterocyclic carbenes have been utilised as highly efficient nucleophilic organocatalysts to mediate vinylogous Mukaiyama/Michael reactions of 2-(trimethylsilyloxy)furan with enones to afford γ-substituted butenolides in 44-99% yield with 3:1-32:1 diastereoselectivity.

Author supplied keywords

Cite

CITATION STYLE

APA

Wang, Y., Du, G. F., Xing, F., Huang, K. W., Dai, B., & He, L. (2015). N-Heterocyclic-Carbene-Catalysed Diastereoselective Vinylogous Mukaiyama/Michael Reaction of 2-(Trimethylsilyloxy)furan and Enones. Asian Journal of Organic Chemistry, 4(12), 1362–1365. https://doi.org/10.1002/ajoc.201500348

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free