Journal
TETRAHEDRON
Volume 68, Issue 38, Pages 7911-7919Publisher
PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.tet.2012.07.013
Keywords
-
Categories
Funding
- Shanghai Municipal Committee of Science and Technology [11JC1402600]
- National Basic Research Program of China [(973)-2010CB833302]
- Fundamental Research Funds for the Central Universities
- National Natural Science Foundation of China [21072206, 20872162, 20672127, 20732008, 21121062, 20702013]
Ask authors/readers for more resources
The [3+2] annulation reactions of 2-arylideneindane-1,3-diones with Morita-Baylis-Hillman (MBH) carbonates proceeded smoothly in the presence of multifunctional thiourea-phosphines to produce the corresponding quaternary carbon centered spirocyclic cyclopentenes in moderate yields, with high diastereoselectivities and enantioselectivities under mild conditions. The plausible reaction has been also discussed on the basis of previous literature. (C) 2012 Elsevier Ltd. All rights reserved.
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