Literature DB >> 16354070

Aryl iodide mediated aziridination of alkenes.

Jiayin Li1, Philip Wai Hong Chan, Chi-Ming Che.   

Abstract

[reaction: see text] Aryl iodide mediated aziridination of a variety of alkenes with N-aminophthalimide under mild conditions (m-CPBA, K2CO3, CH2Cl2, 25 degrees C) was achieved in moderate to good yields (up to 94%). By recovering the aryl iodide, a recyclable system is developed with product yield over 79% attained for the aziridination of trans-1,2-diphenylethylene.

Entities:  

Year:  2005        PMID： 16354070     DOI： 10.1021/ol052293c

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


  3 in total

1.  Scope and mechanism of intramolecular aziridination of cyclopent-3-enyl-methylamines to 1-azatricyclo[2.2.1.0(2,6)]heptanes with lead tetraacetate.

Authors:  Huayou Hu; Juan A Faraldos; Robert M Coates
Journal:  J Am Chem Soc       Date:  2009-08-26       Impact factor: 15.419

2.  Structural Identification between Phthalazine-1,4-Diones and N-Aminophthalimides via Vilsmeier Reaction: Nitrogen Cyclization and Tautomerization Study.

Authors:  Cheng-Yen Chung; Ching-Chun Tseng; Sin-Min Li; Shuo-En Tsai; Hui-Yi Lin; Fung Fuh Wong
Journal:  Molecules       Date:  2021-05-13       Impact factor: 4.411

Review 3.  Electrophilic Aminating Agents in Total Synthesis.

Authors:  Lauren G O'Neil; John F Bower
Journal:  Angew Chem Int Ed Engl       Date:  2021-08-06       Impact factor: 16.823
  3 in total

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