Literature DB >> 28660938

A Pd-catalyzed, boron ester-mediated, reductive cross-coupling of two aryl halides to synthesize tricyclic biaryls.

Zhilong Chen1, Xiaodong Wang1.   

Abstract

Tricyclic biaryls are important scaffold structures in many natural products and lead compounds in drug discovery. The formation of a biaryl unit is often the key step for the synthesis of tricyclic biaryls. Despite significant progress toward the synthesis of biaryl compounds in recent years, the direct cross-coupling of two different aryl halides is still challenging and robust methods are lacking. Herein we report a direct cross-coupling of two different aryl halides in the presence of a palladium catalyst and boron ester, which provides a new and useful complementary method to synthesize tricyclic biaryls.

Entities:  

Year:  2017        PMID: 28660938     DOI: 10.1039/c7ob01237c

Source DB:  PubMed          Journal:  Org Biomol Chem        ISSN: 1477-0520            Impact factor:   3.876


  3 in total

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Journal:  J Enzyme Inhib Med Chem       Date:  2022-12       Impact factor: 5.756

2.  Sulfonate Versus Sulfonate: Nickel and Palladium Multimetallic Cross-Electrophile Coupling of Aryl Triflates with Aryl Tosylates.

Authors:  Kai Kang; Liangbin Huang; Daniel J Weix
Journal:  J Am Chem Soc       Date:  2020-06-08       Impact factor: 15.419

3.  Palladium-catalyzed intramolecular C-H arylation of 2-halo-N-Boc-N-arylbenzamides for the synthesis of N-H phenanthridinones.

Authors:  Quan-Fang Hu; Tian-Tao Gao; Yao-Jie Shi; Qian Lei; Luo-Ting Yu
Journal:  RSC Adv       Date:  2018-04-13       Impact factor: 4.036

  3 in total

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