Convenient, Large-Scale Synthesis of (<i>S</i>)-TRIP Using Suzuki Cross-Coupling Conditions-Reference-Cited by-同舟云学术

Convenient, Large-Scale Synthesis of (S)-TRIP Using Suzuki Cross-Coupling Conditions

Published:2022-01-10 Issue:1 Volume:26 Page:165-173
ISSN:1083-6160
Container-title:Organic Process Research & Development
language:en
Short-container-title:Org. Process Res. Dev.

Author:

Mamidala Ramesh¹,Kommuri Chandrasekhar¹,Paulose Justin¹,Aswath Hema¹,Pawar Lokesh¹,Arunachalampillai Athimoolam¹,Cherney Alan H.²^ORCID,Tedrow Jason S.²^ORCID,Rötheli Andreas R.²^ORCID,Ortiz Adrian³

Affiliation:

1. Syngene Amgen Research & Development Center, Biocon Park, Plot No. 2 & 3, Bommasandra IV Phase, Jigni Link Road, Bangalore 560099, India

2. Process Development, Amgen, Inc., 360 Binney Street, Cambridge, Massachusetts 02142, United States

3. Process Development, Amgen, Inc., 1 Amgen Center Dr, Thousand Oaks, California 91320, 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.1c00386

Reference32 articles.

1. BINOL: A Versatile Chiral Reagent

2. Modified BINOL Ligands in Asymmetric Catalysis

3. Enantioselective Fluorescent Sensors: A Tale of BINOL

4. Chiral Phosphoric Acids as Versatile Catalysts for Enantioselective Transformations

5. Chiral Brønsted Acids for Asymmetric Organocatalysis

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1. A convenient synthetic approach to highly hindered 3,3′-bis(2,4,6-tri-tert-butylphenyl)-BINOL-derived phosphoric acids;New Journal of Chemistry;2024

2. Decarboxylative Iodination and Suzuki-Miyaura Coupling Reactions to Access Chiral 3,3′-Diaryl-1,1′-bi-2-naphthols;The Journal of Organic Chemistry;2023-12-08

3. Bulky, electron-rich, renewable: analogues of Beller's phosphine for cross-couplings;Catalysis Science & Technology;2023