Abstract

We report the copper-catalyzed asymmetric conjugate addition of vinyl arene-derived nucleophiles to α,β-unsaturated diesters. Due to the high electrophilicity of α,β-unsaturated diesters toward nucleophilic copper catalysts, inclusion of vinyl arenes as pronucleophiles is challenging due to chemoselectivity issues in a multicomponent reaction compared with those of other successful examples of dienes, allenes, and enynes. In this method, chemoselective in situ generation of a chiral benzylic copper intermediate and its stereoselective addition to α,β-unsaturated diesters provided organoboron adducts with contiguous stereogenic centers with good levels of diastereoselectivity and enantioselectivity (≤85:15 diastereomeric ratio and 99% enantiomeric excess, respectively).

Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.