The Mechanism and Origin of Enantioselectivity in the Rhodium-Catalyzed Asymmetric Ring-Opening Reactions of Oxabicyclic Alkenes with Organoboronic Acids: A DFT Investigation-Reference-Cited by-同舟云学术

The Mechanism and Origin of Enantioselectivity in the Rhodium-Catalyzed Asymmetric Ring-Opening Reactions of Oxabicyclic Alkenes with Organoboronic Acids: A DFT Investigation

Published:2021-05-28 Issue:11 Volume:40 Page:1588-1597
ISSN:0276-7333
Container-title:Organometallics
language:en
Short-container-title:Organometallics

Author:

Pounder Austin¹,Tam William¹,Chen Leanne D.¹^ORCID

Affiliation:

1. Guelph-Waterloo Centre for Graduate Work in Chemistry and Biochemistry, Department of Chemistry, University of Guelph, Guelph, Ontario N1G 2W1, Canada

Funder

Natural Sciences and Engineering Research Council of Canada

Publisher

American Chemical Society (ACS)

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.organomet.1c00017

Reference93 articles.

1. Recent Advances in Transition Metal-Catalyzed Reactions of Oxabenzonorbornadiene

2. New Catalytic Reactions of Oxa- and Azabicyclic Alkenes

3. Transition Metal-Catalyzed Enantioselective Ring-Opening Reactions of Oxabicyclic Alkenes

4. Chemistry of Unsymmetrical C1-Substituted Oxabenzonorbornadienes

5. Catalytic asymmetric transformations of oxa- and azabicyclic alkenes

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