Literature DB >> 17539682

Unexpected reactivity of the burgess reagent with thiols: synthesis of symmetrical disulfides.

Scott C Banfield1, Alvaro Takeo Omori, Hannes Leisch, Tomas Hudlicky.   

Abstract

Reaction of the Burgess reagent with a series of aliphatic and aromatic thiols led to the corresponding symmetrical disulfides in high yields. No olefins were detected in the reactions of aliphatic thiols.

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Year:  2007        PMID: 17539682     DOI: 10.1021/jo070099t

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


  2 in total

1.  Homocouplings of Sodium Arenesulfinates: Selective Access to Symmetric Diaryl Sulfides and Diaryl Disulfides.

Authors:  Xin-Zhang Yu; Wen-Long Wei; Yu-Lan Niu; Xing Li; Ming Wang; Wen-Chao Gao
Journal:  Molecules       Date:  2022-09-22       Impact factor: 4.927

2.  Dipotassium 1,3,4-thiadiazole-2,5-bis(thiolate) as a new S-donor for direct synthesis of symmetrical disulfides.

Authors:  Mohammad Soleiman-Beigi; Mohammad Alikarami; Homa Kohzadi; Zahra Akbari
Journal:  Sci Rep       Date:  2022-09-27       Impact factor: 4.996

  2 in total

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