4.6 Article

Transition-metal-free synthesis of 1,1-diboronate esters with a fully substituted benzylic center via diborylation of lithiated carbamates

Journal

ORGANIC & BIOMOLECULAR CHEMISTRY
Volume 15, Issue 16, Pages 3418-3422

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/c7ob00654c

Keywords

-

Funding

  1. National Natural Science Foundation of China [21573262]
  2. Natural Science Foundation of Jiangsu Province [BK20161259]
  3. MOE SAFEA [B13025]

Ask authors/readers for more resources

A transition-metal-free lithiation-borylation method has been developed to access a variety of 1,1-diboronate esters with a fully substituted benzylic center from readily available secondary benzylic N,N-diisopropyl carbamates. The method is applicable to scale-up synthesis of 1,1-diboron compounds. Furthermore, the current method is also applicable to synthesizing optically active 1,1-silylboronate esters.

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