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Enantio- and diastereoselective synthesis of spiro-epoxyoxindoles.
- Source :
-
The Journal of organic chemistry [J Org Chem] 2014 May 02; Vol. 79 (9), pp. 3924-9. Date of Electronic Publication: 2014 Apr 23. - Publication Year :
- 2014
-
Abstract
- An asymmetric synthesis of epoxyoxindoles from isatins has been developed by employing chiral sulfur ylides generated in situ from camphor-derived sulfonium salts. This reaction allows an efficient access to enantioenriched spiro-epoxyoxindoles under mild reaction conditions, featuring high yields and excellent enantio- and diastereoselectivities.
Details
- Language :
- English
- ISSN :
- 1520-6904
- Volume :
- 79
- Issue :
- 9
- Database :
- MEDLINE
- Journal :
- The Journal of organic chemistry
- Publication Type :
- Academic Journal
- Accession number :
- 24730463
- Full Text :
- https://doi.org/10.1021/jo5003856