Literature DB >> 27572058

Iridium(III)-Catalyzed Regioselective C7-Amination of N-Pivaloylindoles with Sulfonoazides.

Lanting Xu1, Lushi Tan2, Dawei Ma1.   

Abstract

Direct C7-amination of N-pivaloylindoles has been achieved using a combination of [Cp*IrCl2]2, AgNTf2, and AgOAc as the catalyst and sulfonoazides as the nitrogen source. The reaction proceeded at room temperature to 80 °C to afford 7-sulfonamidoindoles in good to excellent yields. The reaction is broadly applicable to the C7-amination of a wide variety of 3-, 4-, 5-, and 6-substituted N-pivaloylindoles with either alkyl or aryl sulfonoazides.

Entities:  

Year:  2016        PMID: 27572058     DOI: 10.1021/acs.joc.6b01856

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


  2 in total

1.  Concise Synthesis of (-)-Hodgkinsine, (-)-Calycosidine, (-)-Hodgkinsine B, (-)-Quadrigemine C, and (-)-Psycholeine via Convergent and Directed Modular Assembly of Cyclotryptamines.

Authors:  Petra Lindovska; Mohammad Movassaghi
Journal:  J Am Chem Soc       Date:  2017-11-20       Impact factor: 15.419

2.  Total Synthesis and Stereochemical Assignment of (-)-Psychotridine.

Authors:  Tony Z Scott; Vinicius F Armelin; Mohammad Movassaghi
Journal:  Org Lett       Date:  2022-03-17       Impact factor: 6.072

  2 in total

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