Literature DB >> 15104466

A convenient tin-free procedure for radical carboazidation and azidation.

Philippe Panchaud1, Philippe Renaud.   

Abstract

The radical carboazidation of alkenes has been achieved in water with triethylborane as initiator. This efficient process is complete in 1 h at room temperature in an open system. These new tin-free carboazidation conditions are environmentally friendly and allow running reactions with an excess of either the alkene or the radical precursor. They are also suitable for simple radical azidation of alkyl iodides as well as for more complex cascade reactions involving annulation processes.

Entities:  

Year:  2004        PMID: 15104466     DOI: 10.1021/jo0498720

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


  3 in total

1.  Versatile Enantioselective Synthesis of Functionalized Lactones via Copper-Catalyzed Radical Oxyfunctionalization of Alkenes.

Authors:  Rong Zhu; Stephen L Buchwald
Journal:  J Am Chem Soc       Date:  2015-06-23       Impact factor: 15.419

2.  Palladium-Catalyzed Cross Coupling of Secondary and Tertiary Alkyl Bromides with a Nitrogen Nucleophile.

Authors:  D Matthew Peacock; Casey B Roos; John F Hartwig
Journal:  ACS Cent Sci       Date:  2016-09-01       Impact factor: 14.553

3.  Two-Step Azidoalkenylation of Terminal Alkenes Using Iodomethyl Sulfones.

Authors:  Nicolas Millius; Guillaume Lapointe; Philippe Renaud
Journal:  Molecules       Date:  2019-11-18       Impact factor: 4.411

  3 in total

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