Literature DB >> 31074279

One-Pot, Three-Component Synthesis of 5-Sulfenyl-2-iminothiazolines by Cross-Dehydrogenative C-S Coupling Using I2/DMSO in Open Air.

Chandan Bodhak1, Animesh Pramanik1.   

Abstract

A one-pot, three-component, transition-metal-free regioselective sulfenylation of 2-iminothiazoline through the cross-dehydrogenative coupling strategy via sp2 C-H functionalization has been developed employing iodine as a catalyst and dimethyl sulfoxide as an oxidant. Utility of this sulfenylation technique has been well depicted through participation of various aryl and heterocyclic thiols. Significant features of this C-H functionalization strategy include metal-free open air reaction conditions, which offer a mild and efficient method for sulfenylation to achieve diversely substituted 5-sulfenyl-2-iminothiazoline derivatives.

Entities:  

Year:  2019        PMID: 31074279     DOI: 10.1021/acs.joc.9b00785

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


  3 in total

Review 1.  Application of phenacyl bromide analogs as a versatile organic intermediate for the synthesis of heterocyclic compounds via multicomponent reactions.

Authors:  Ramin Javahershenas
Journal:  Mol Divers       Date:  2022-10-13       Impact factor: 3.364

2.  Mild and Expeditious Synthesis of Sulfenyl Enaminones of l-α-Amino Esters and Aryl/Alkyl Amines through NCS-Mediated Sulfenylation.

Authors:  Sayan Mukherjee; Animesh Pramanik
Journal:  ACS Omega       Date:  2021-11-30

3.  A mild one-pot synthesis of 2-iminothiazolines from thioureas and 1-bromo-1-nitroalkenes.

Authors:  Yuan Xu; Xin Ge; Yuhan Zhang; Hongbin Zhang; Xue-Wei Liu
Journal:  RSC Adv       Date:  2021-01-08       Impact factor: 3.361

  3 in total

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