Journal
ORGANIC LETTERS
Volume 23, Issue 24, Pages 9485-9489Publisher
AMER CHEMICAL SOC
DOI: 10.1021/acs.orglett.1c03674
Keywords
-
Categories
Funding
- Canada Foundation for Innovation [35261, 19119]
- Ontario Research Fund
- University of Toronto
- NSERC
Ask authors/readers for more resources
A Negishi cross-coupling method has been developed for the synthesis of alpha-aryl ester products using alpha-hydroxy ester derivatives and arylzinc reagents. This reaction is efficient, rapid, and mild, providing a complementary way of accessing desirable products.
A Negishi cross-coupling of alpha-hydroxy ester derivatives and arylzinc reagents has been developed. This reaction tolerates both primary and secondary C(sp(3))-O alcohol precursors and achieves efficient cross-coupling under Ni catalysis without the need for added external metal reductant, photocatalyst, or additives. The arylation of readily accessible C(sp(3))-O electrophiles in this operationally simple, rapid, and mild reaction provides a complementary way of accessing desirable alpha-aryl ester products.
Authors
I am an author on this paper
Click your name to claim this paper and add it to your profile.
Reviews
Recommended
No Data Available