Regioselective Cu-Catalyzed Hydroboration of 1,3-Disubstituted-1,3-Dienes: Functionalization of Conjugated Dienes Readily Accessible through Ene

Regioselective Cu-Catalyzed Hydroboration of 1,3-Disubstituted-1,3-Dienes: Functionalization of Conjugated Dienes Readily Accessible through Ene–Yne Metathesis

Published:2022-05-13 Issue:11 Volume:12 Page:6434-6443
ISSN:2155-5435
Container-title:ACS Catalysis
language:en
Short-container-title:ACS Catal.

Author:

Xu Ruoshui¹,Rohde Laurence N.¹,Diver Steven T.¹^ORCID

Affiliation:

1. Department of Chemistry, University at Buffalo, the State University of New York, Amherst, New York 14260-3000, United States

Funder

Division of Chemistry

Publisher

American Chemical Society (ACS)

Subject

Catalysis,General Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acscatal.2c01190

Reference37 articles.

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2. a A notable exception is the work of Brown et al. who are able to control regiochemistry of copper borylation using a Cu(I) N-heterocyclic carbene, as applied to a Cu/Pd arylboration reaction.

3. Catalyst Controlled Regiodivergent Arylboration of Dienes

4. Expanded Scope in Ethylene−Alkyne Cross-Metathesis: Coordinating Heteroatom Functionality at the Propargylic Position

5. Enyne Metathesis (Enyne Bond Reorganization)

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