Literature DB >> 15369365

3-pyridylcarbene and 3-pyridylnitrene: ring opening to nitrile ylides.

Pawel Bednarek1, Curt Wentrup.   

Abstract

Photolysis of 3-pyridyldiazomethane in an Ar matrix at 7-10 K gives 3-pyridylcarbene. Further photolysis causes ring opening to nitrile ylide 26 (formonitrile pent-2-en-4-ynylide) as the major reaction together with a minor amount of ring expansion to 1-azacyclohepta-1,3,4,6-tetraene, 27. Matrix photolysis of 3-azidopyridine leads to ring opening to formonitrile N-cyanovinylmethylide, 33.

Entities:  

Year:  2003        PMID: 15369365     DOI: 10.1021/ja035632a

Source DB:  PubMed          Journal:  J Am Chem Soc        ISSN: 0002-7863            Impact factor:   15.419


  2 in total

1.  4-Pyridylnitrene and 2-pyrazinylcarbene.

Authors:  Curt Wentrup; Ales Reisinger; David Kvaskoff
Journal:  Beilstein J Org Chem       Date:  2013-04-17       Impact factor: 2.883

2.  3-Pyridylnitrene, 2- and 4-pyrimidinylcarbenes, 3-quinolylnitrenes, and 4-quinazolinylcarbenes. Interconversion, ring expansion to diazacycloheptatetraenes, ring opening to nitrile ylides, and ring contraction to cyanopyrroles and cyanoindoles.

Authors:  Curt Wentrup; Nguyen Mong Lan; Adelheid Lukosch; Pawel Bednarek; David Kvaskoff
Journal:  Beilstein J Org Chem       Date:  2013-04-17       Impact factor: 2.883

  2 in total

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