4.8 Article

Organocatalyzed Intermolecular Asymmetric Allylic Dearomatization of Both α- and β-Naphthols

Journal

ORGANIC LETTERS
Volume 21, Issue 1, Pages 330-334

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.orglett.8b03934

Keywords

-

Funding

  1. NSFC [21672184, 21861042]
  2. Program for Changjiang Scholars and Innovative Research Team in University [IRT13095]
  3. Program for Innovative Research Team (in Science and Technology) in University of Yunnan Province, Yunling Scholar of Yunnan Province, Yunnan Province Government [2018FY001(016)]
  4. National Postdoctoral Program for Innovative Talents [BX201600129]
  5. China Postdoctoral Science Foundation [2016M602726]

Ask authors/readers for more resources

The first highly stereoselective intermolecular catalytic asymmetric dearomatization (CADA) of alpha-naphthols through C-C formation and the first asymmetric allylic dearomatization of naphthols by chiral organocatalysis have been achieved. These new and complete atom-economic reactions provide enantioriched alpha- and beta-naphthalenones bearing an all-carbon quaternary center.

Authors

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

Reviews

Primary Rating

4.8
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available