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A new versatile approach to synthesise enantioenriched 3-hydroxyoxindoles, 1,3-dihydroisobenzofuran and 3-isochromanone derivatives by a rhodium-catalyzed asymmetric arylation-cyclization sequenceElectronic supplementary information (ESI) available: Experimental procedures and spectral data. See DOI: 10.1039/c3cc47927g

A novel arylationcyclization strategy for the highly enantioselective synthesis of titled heterocycles with a quaternary stereogenic center has been developed. A novel arylation-cyclization strategy for the highly enantioselective synthesis of titled pharmaceutically attractive chiral heterocycles w...

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Bibliographic Details
Main Authors: Li, Yi, Zhu, Dong-Xing, Xu, Ming-Hua
Format: Article
Language:English
Online Access:Get full text
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Summary:A novel arylationcyclization strategy for the highly enantioselective synthesis of titled heterocycles with a quaternary stereogenic center has been developed. A novel arylation-cyclization strategy for the highly enantioselective synthesis of titled pharmaceutically attractive chiral heterocycles with a tetrasubstituted stereogenic center has been developed.
ISSN:1359-7345
1364-548X
DOI:10.1039/c3cc47927g