Journal
ORGANIC LETTERS
Volume 19, Issue 18, Pages 4884-4887Publisher
AMER CHEMICAL SOC
DOI: 10.1021/acs.orglett.7b02341
Keywords
-
Categories
Funding
- NNSFC [21232004, 21620102003]
- STCSM [15JC1402200]
- SHMEC [201701070002E00030]
Ask authors/readers for more resources
A highly efficient (aS)-Ir/In-BiphPHOX-catalyzed asymmetric hydrogenation of substituted 2H-chromenes and substituted benzo[e][1,2]oxathiine 2,2-dioxides is described. A series of 2H-chromenes and benzo [e] [1,2]oxathiine 2,2-dioxides were hydrogenated to give the target products in high yields (92-99%) with excellent enantioselectivities (up to 99.7% ee) using our catalytic system. This reaction provides a direct and efficient method for the construction of chiral bent six-membered oxygen-containing compounds.
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