Literature DB >> 22458413

Palladium-catalyzed C-N cross coupling of sulfinamides and aryl halides.

Xiaofei Sun1, Xingzhao Tu, Chuan Dai, Xiaoping Zhang, Binbin Zhang, Qingle Zeng.   

Abstract

The palladium-catalyzed C-N cross coupling of sulfinamides and aryl halides is reported. In the presence of Pd(2)(dba)(3), tBuXPhos, NaOH, and a small amount of water, the C-N cross coupling of chiral tert-butanesulfinamide and aryl halides was accomplished to give N-aryl tert-butanesulfinamide without racemization, and the coupling of racemic p-toluenesulfinamide smoothly afforded N-aryl p-toluenesulfinamides. 2-Bromopyridine was also suitable for the coupling. Addition of a small amount of water to the catalytic system was of importance to obtain high yields.

Entities:  

Year:  2012        PMID: 22458413     DOI: 10.1021/jo3003584

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


  3 in total

Review 1.  Applications of Palladium-Catalyzed C-N Cross-Coupling Reactions.

Authors:  Paula Ruiz-Castillo; Stephen L Buchwald
Journal:  Chem Rev       Date:  2016-09-30       Impact factor: 60.622

2.  (S)-N-Phenyl-tert-butane-sulfinamide.

Authors:  Xiaofei Sun; Xiaoping Zhang; Binbin Zhang; Wenguo Wang; Qingle Zeng
Journal:  Acta Crystallogr Sect E Struct Rep Online       Date:  2012-05-16

3.  Ring-Closure Mechanisms Mediated by Laccase to Synthesize Phenothiazines, Phenoxazines, and Phenazines.

Authors:  Veronika Hahn; Annett Mikolasch; Josephine Weitemeyer; Sebastian Petters; Timo Davids; Michael Lalk; Jan-Wilm Lackmann; Frieder Schauer
Journal:  ACS Omega       Date:  2020-06-08
  3 in total

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