3-pyridylcarbene and 3-pyridylnitrene: Ring opening to nitrile ylides


Autoria(s): Bednarek, P.; Wentrup, C.
Data(s)

01/01/2003

Resumo

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.

Identificador

http://espace.library.uq.edu.au/view/UQ:65620

Idioma(s)

eng

Publicador

American Chemical Society

Palavras-Chave #Ab-initio #Carbene #Chemistry, Multidisciplinary #Density-functional Theory #Energy Surface #Expansion #Interconversion #Nitrene Rearrangements #Phenylcarbene #Phenylnitrene #Photochemistry #C1 #250303 Physical Organic Chemistry #780103 Chemical sciences #0399 Other Chemical Sciences
Tipo

Journal Article