Literature DB >> 34128009

A multicomponent tetrazolo indole synthesis.

Xiaofang Lei1, Panagiota Lampiri2, Pravin Patil3, Giasemi Angeli2, Constantinos G Neochoritis2, Alexander Dömling3.   

Abstract

The ubiquitous presence of the indole fragment in natural products and drugs asks for ever novel syntheses. We report an unprecedented mild, two-step synthesis of 2-tetrazolo substituted indoles based on the Ugi-tetrazole reaction combined with an acidic ring closure. A gram-scale synthesis, a bioactive compound and further transformations were performed.

Entities:  

Year:  2021        PMID: 34128009     DOI: 10.1039/d1cc02384e

Source DB:  PubMed          Journal:  Chem Commun (Camb)        ISSN: 1359-7345            Impact factor:   6.222


  2 in total

1.  A One-Pot Six-Component Reaction for the Synthesis of 1,5-Disubstituted Tetrazol-1,2,3-Triazole Hybrids and Their Cytotoxic Activity against the MCF-7 Cell Line.

Authors:  Cesia M Aguilar-Morales; Jorge Gustavo Araujo-Huitrado; Yamilé López-Hernández; Claudia Contreras-Celedón; Alejandro Islas-Jácome; Angelica Judith Granados-López; Cesar R Solorio-Alvarado; Jesús Adrián López; Luis Chacón-García; Carlos J Cortés-García
Journal:  Molecules       Date:  2021-10-10       Impact factor: 4.411

2.  Highly Stereoselective Ugi/Pictet-Spengler Sequence.

Authors:  Bidong Zhang; Katarzyna Kurpiewska; Alexander Dömling
Journal:  J Org Chem       Date:  2022-05-12       Impact factor: 4.198

  2 in total

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