| Literature DB >> 26403641 |
Srimoyee Dasgupta1, Thomas Rivas1, Mary P Watson2.
Abstract
An enantioselective, copper(I)-catalyzed addition of terminal alkynes to isochroman ketals to set diaryl, tetrasubstituted stereocenters has been developed. The success of this reaction relies on identification of a Cu/PyBox catalyst capable of distinguishing the faces of the diaryl-substituted oxocarbenium ion. This challenging transformation enables efficient conversion of readily available, racemic ketals into high-value enantioenriched isochroman products with fully substituted stereogenic centers. High yields and enantiomeric excesses are observed for various isochroman ketals and an array of alkynes.Entities:
Keywords: alkynes; asymmetric catalysis; enantioselectivity; oxocarbenium ion; oxygen heterocycles
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Year: 2015 PMID: 26403641 PMCID: PMC4819992 DOI: 10.1002/anie.201507373
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336