Literature DB >> 21542601

Ionic diamine rhodium complex catalyzed reductive N-heterocyclization of 2-nitrovinylarenes.

Kazumi Okuro1, Joanna Gurnham, Howard Alper.   

Abstract

Ionic diamine rhodium complex (1) catalyzes the reductive N-cyclization of 2-vinylnitroarenes using carbon monoxide as a reducing agent to afford functionalized indoles. The catalytic system allows direct access to indoles with ester and ketone groups at the 2- or 3-position, in good yields.

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Year:  2011        PMID: 21542601     DOI: 10.1021/jo200320k

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


  3 in total

1.  An efficient and selective microwave-assisted Claisen-Schmidt reaction for the synthesis of functionalized benzalacetones.

Authors:  Anita Rayar; Maité Sylla-Iyarreta Veitía; Clotilde Ferroud
Journal:  Springerplus       Date:  2015-05-14

2.  Synthesis of Cyclic Peptides in SPPS with Npb-OH Photolabile Protecting Group.

Authors:  Tingting Chen; Gang Wang; Lin Tang; Hongpeng Yang; Jing Xu; Xiaoxue Wen; Yunbo Sun; Shuchen Liu; Tao Peng; Shouguo Zhang; Lin Wang
Journal:  Molecules       Date:  2022-03-29       Impact factor: 4.411

3.  Counterion Control of t-BuO-Mediated Single Electron Transfer to Nitrostilbenes to Construct N-Hydroxyindoles or Oxindoles.

Authors:  Yingwei Zhao; Haoran Zhu; Siyoung Sung; Donald J Wink; Joseph M Zadrozny; Tom G Driver
Journal:  Angew Chem Int Ed Engl       Date:  2021-07-20       Impact factor: 16.823

  3 in total

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