Development and Scale-up of an Efficient Miyaura Borylation Process Using Tetrahydroxydiboron-Reference-Cited by-同舟云学术

Development and Scale-up of an Efficient Miyaura Borylation Process Using Tetrahydroxydiboron

Published:2016-12-13 Issue:1 Volume:21 Page:65-74
ISSN:1083-6160
Container-title:Organic Process Research & Development
language:en
Short-container-title:Org. Process Res. Dev.

Author:

Gurung Sing R.¹,Mitchell Christopher²,Huang Jie¹,Jonas Marco¹,Strawser Josiah D.²,Daia Elena³,Hardy Andrew²,O’Brien Erin²,Hicks Frederick²,Papageorgiou Charles D.²^ORCID

Affiliation:

1. Albany Molecular Research Inc., 21 Corporate Circle, Albany, New York 12203, United States

2. Takeda Pharmaceuticals International Co., Process Chemistry, 40 Landsdowne Street, Cambridge, Massachusetts 02139, United States

3. Carbogen AMCIS Ltd., 303 Clayton Lane, Manchester, M11 4SX, United Kingdom

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.oprd.6b00345

Reference21 articles.

1. Palladium Catalysts for the Suzuki Cross-Coupling Reaction: An Overview of Recent Advances

2. Recent applications of the Suzuki–Miyaura cross-coupling reaction in organic synthesis

3. Palladium(0)-Catalyzed Cross-Coupling Reaction of Alkoxydiboron with Haloarenes: A Direct Procedure for Arylboronic Esters

4. Novel Palladium(0)-Catalyzed Coupling Reaction of Dialkoxyborane with Aryl Halides: Convenient Synthetic Route to Arylboronates

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