4.6 Article

Pinacol Rearrangement and Direct Nucleophilic Substitution of Allylic Alcohols Promoted by Graphene Oxide and Graphene Oxide CO2H

Journal

CHEMCATCHEM
Volume 9, Issue 6, Pages 1032-1039

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/cctc.201601362

Keywords

allylic compounds; carbocations; graphene; green chemistry; rearrangement

Funding

  1. University of Alicante [UAUSTI16-03, VIGROB-173]
  2. Spanish Ministerio de Economia y Competitividad [CTQ2015-66624-P]

Ask authors/readers for more resources

Graphene oxide (GO) and carboxylic acid functionalized GO (GO-CO2H) have been found to efficiently promote the heterogeneous and environmentally friendly pinacol rearrangement of 1,2-diols and the direct nucleophilic substitution of allylic alcohols. In general, high yields and regioselectivities are obtained in both reactions using 20 wt% of catalyst loading and mild reaction conditions.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.6
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available