Literature DB >> 26166246

Palladacycle-Catalyzed Carbonylative Suzuki-Miyaura Coupling with High Turnover Number and Turnover Frequency.

Prashant Gautam1, Bhalchandra M Bhanage1.   

Abstract

This work reports the carbonylative Suzuki-Miyaura coupling of aryl iodides catalyzed by palladacycles. More importantly, the palladacycles have been used to generate high turnover numbers (TON's) and turnover frequencies (TOF's). A range of aryl iodides can be coupled with arylboronic acids, generating TON's in the range of 10(6) to 10(7) and TOF's in the range of 10(5) to 10(6) h(-1). Comparison of the palladacycles with a conventional palladium source shows their superiority in generating high TON's and TOF's.

Entities:  

Year:  2015        PMID: 26166246     DOI: 10.1021/acs.joc.5b01160

Source DB:  PubMed          Journal:  J Org Chem        ISSN: 0022-3263            Impact factor:   4.354


  2 in total

1.  Synthesis of unprotected glyco-alkynones via molybdenum-catalyzed carbonylative Sonogashira cross-coupling reaction.

Authors:  Mariana P Darbem; Henrique A Esteves; Robert A Burrow; Antônio A Soares-Paulino; Daniel C Pimenta; Hélio A Stefani
Journal:  RSC Adv       Date:  2022-01-13       Impact factor: 3.361

2.  Direct Dehydrogenative Access to Unsymmetrical Phenones.

Authors:  Congjun Yu; Raolin Huang; Frederic W Patureau
Journal:  Angew Chem Int Ed Engl       Date:  2022-03-19       Impact factor: 16.823

  2 in total

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