Literature DB >> 30471673

Homologation of Ugi and Passerini reactions using ynamides.

Bo Huang1, Sunliang Cui2.   

Abstract

Being important biological and pharmacological units, β-amino amides and β-acyloxy amides have a privileged position in both academia and industry. Developing a methods to prepare them has gained attention. Ynamides, which possess dual nucleophilic and electrophilic properties, are similar to isonitriles. In this review, usage of ynamides in the single reactant replacement approach of Ugi and Passerini reactions to develop two new multicomponent reactions to get various β-amino amides and β-acyloxy amides is reported.
Copyright © 2018 Elsevier Ltd. All rights reserved.

Entities:  

Mesh:

Substances:

Year:  2018        PMID: 30471673     DOI: 10.1016/j.ddtec.2018.09.001

Source DB:  PubMed          Journal:  Drug Discov Today Technol        ISSN: 1740-6749


  1 in total

1.  Green synthesis, crystal structure, and antifungal activities of (E)-4-arylidene-5-oxotetrahydrofuran.

Authors:  Yun Dong; Ling-Qi Kong; Qin-Hua Chen; Bin Li; Xiao-Hua Zeng; Li-Na Ke; Hong-Mei Wang
Journal:  Front Chem       Date:  2022-09-09       Impact factor: 5.545

  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.