Literature DB >> 28920113

Double 1,4-addition of (thio)salicylamides/thiosalicylic acids with propiolate derivatives: a direct, general synthesis of diverse heterocyclic scaffolds.

Hui-Hong Wang1, Tao Shi, Wei-Wei Gao, Hong-Hua Zhang, Yong-Qiang Wang, Jun-Fang Li, Yong-Sheng Hou, Jin-Hong Chen, Xue Peng, Zhen Wang.   

Abstract

A simple and practical ring-closure procedure to prepare a range of diverse heterocycles has been developed. In this transformation, a variety of substituted (thio)salicylamides and thiosalicylic acids undergo a double 1,4-addition reaction with propiolate derivatives in the presence of an inorganic base (K3PO4), as a result benzothiazinones, benzoxazinones and benzoxathiinones were prepared in good to excellent yields, respectively, even in gram scales. In addition, further transformation towards more complex structures and oxicam drug analogues has also been successfully carried out.

Entities:  

Year:  2017        PMID: 28920113     DOI: 10.1039/c7ob02101a

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


  2 in total

1.  Synthesis of functionalized benzo[1,3]dioxin-4-ones from salicylic acid and acetylenic esters and their direct amidation.

Authors:  Rasmi P Bhaskaran; Kalinga H Nayak; Beneesh P Babu
Journal:  RSC Adv       Date:  2021-07-13       Impact factor: 4.036

2.  Crystal structures of two 2,3-diaryl-2,3-di-hydro-4H-1,3-benzo-thia-zin-4-ones.

Authors:  Hemant P Yennawar; Michaela J Buchwalter; Baylee K Colburn; Lee J Silverberg
Journal:  Acta Crystallogr E Crystallogr Commun       Date:  2018-02-20
  2 in total

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