Development of an Efficient Process to Prepare Methyl 4,5,6-Trichloropicolinate Using Highly Selective C–H Borylation/Chlorodeborylation Reactions-Reference-Cited by-同舟云学术

Development of an Efficient Process to Prepare Methyl 4,5,6-Trichloropicolinate Using Highly Selective C–H Borylation/Chlorodeborylation Reactions

Published:2022-10-11 Issue:10 Volume:26 Page:2957-2964
ISSN:1083-6160
Container-title:Organic Process Research & Development
language:en
Short-container-title:Org. Process Res. Dev.

Author:

Li Xiaoyong¹^ORCID,Wiensch Eric¹,Oppenheimer Jossian²

Affiliation:

1. Process Sciences & Technology, Small Molecule Discovery & Development, Corteva AgriScience, 9330 Zionsville Rd., Indianapolis, Indiana 46268, United States

2. Process Sciences & Technology, Small Molecule Discovery & Development, Corteva AgriScience, Midland, Michigan 48674, United States

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.oprd.2c00247

Reference23 articles.

1. Steric and Chelate Directing Effects in Aromatic Borylation

2. Isolated Ir(V) Boryl Complexes and Their Reactions with Hydrocarbons

3. Remarkably Selective Iridium Catalysts for the Elaboration of Aromatic C-H Bonds

4. Mild Iridium-Catalyzed Borylation of Arenes. High Turnover Numbers, Room Temperature Reactions, and Isolation of a Potential Intermediate

5. A Stoichiometric Aromatic CH Borylation Catalyzed by Iridium( I )/2,2′‐Bipyridine Complexes at Room Temperature

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