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Catalytic asymmetric [2+2] cycloaddition between quinones and fulvenes and a subsequent stereoselective isomerization to 2,3-dihydrobenzofurans.
- Source :
-
Chemical Communications . 6/21/2017, Vol. 53 Issue 49, p6585-6588. 4p. - Publication Year :
- 2017
-
Abstract
- The catalytic enantioselective [2+2] cycloaddition between quinones and fulvenes was achieved, for the first time, by the use of a chiral copper(ii) complex catalyst. The transformation afforded a series of enantiomerically enriched [6,4,5]-tricyclic cyclobutane derivatives in good yields with excellent regio- and stereoselectivities. Furthermore, the [2+2] adducts could be easily converted into formal [3+2] adducts efficiently and stereoselectively. [ABSTRACT FROM AUTHOR]
- Subjects :
- *RING formation (Chemistry)
*STEREOSELECTIVE reactions
*CYCLOBUTANE
Subjects
Details
- Language :
- English
- ISSN :
- 13597345
- Volume :
- 53
- Issue :
- 49
- Database :
- Academic Search Index
- Journal :
- Chemical Communications
- Publication Type :
- Academic Journal
- Accession number :
- 123636444
- Full Text :
- https://doi.org/10.1039/c7cc03211k