Literature DB >> 31553193

Electrochemically Enabled C3-Formylation and -Acylation of Indoles with Aldehydes.

Liquan Yang1, Zhaoran Liu1, Yujun Li1, Ning Lei1, Yanling Shen1, Ke Zheng1.   

Abstract

Reported herein is an effective strategy for oxidative cross-coupling of indoles with various aldehydes. The strategy is based on a two-step transformation via a well-known Mannich-type reaction and a C-N bond cleavage for carbonyl introduction. The key step-the C-N bond cleavage of the Mannich product-was enabled by electrochemistry. This strategy (with over 40 examples) ensures excellent functional-group tolerance as well as late-stage functionalization of pharmaceutical molecules.

Entities:  

Year:  2019        PMID: 31553193     DOI: 10.1021/acs.orglett.9b02433

Source DB:  PubMed          Journal:  Org Lett        ISSN: 1523-7052            Impact factor:   6.005


  2 in total

1.  Graphene oxide-iridium nanocatalyst for the transformation of benzylic alcohols into carbonyl compounds.

Authors:  Tsun-Ren Chen; Yi-Sheng Lin; Yu-Xiang Wang; Wen-Jen Lee; Kelvin H-C Chen; Jhy-Der Chen
Journal:  RSC Adv       Date:  2020-01-27       Impact factor: 4.036

2.  Rhodaelectro-catalyzed access to chromones via formyl C-H activation towards peptide electro-labeling.

Authors:  Maximilian Stangier; Antonis M Messinis; João C A Oliveira; Hao Yu; Lutz Ackermann
Journal:  Nat Commun       Date:  2021-08-05       Impact factor: 14.919

  2 in total

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