3-pyridylcarbene and 3-pyridylnitrene: Ring opening to nitrile ylides
Data(s) |
01/01/2003
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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 | |
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 |