Journal
ORGANIC & BIOMOLECULAR CHEMISTRY
Volume 15, Issue 34, Pages 7097-7101Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/c7ob01820g
Keywords
-
Categories
Funding
- National Natural Science Foundation of China [21672109, 21472097, 21421062]
- Natural Science Foundation of Tianjin [15JCYBJC20000]
Ask authors/readers for more resources
A highly enantioselective intramolecular Rauhut-Currier reaction catalyzed by a multifunctional chiral aminophosphine catalyst was reported. A series of hydro-2H-indole derivatives that bear an all-carbon quaternary center were obtained in high yields (up to 94%), and excellent diastereo- and enantioselectivities (up to > 20:1 dr and > 99% ee). And this reaction could be performed on a gram scale using 2 mol% catalyst loading.
Authors
I am an author on this paper
Click your name to claim this paper and add it to your profile.
Reviews
Recommended
No Data Available