Reaction of carbene of cyclohexadienone type with multiple bonds of conjugated dienes

Autor:	V. V. Ershov, B. D. Sviridov, G. A. Nikiforov
Rok vydání:	1974
Předmět:	chemistry.chemical_compound chemistry Thermal decomposition Photodissociation General Chemistry Conjugated system Photochemistry Multiple bonds Isomerization Carbene Quinone
Zdroj:	Bulletin of the Academy of Sciences of the USSR Division of Chemical Science. 23:339-342
ISSN:	1573-9171 0568-5230
DOI:	10.1007/bf00924683
Popis:	1. The 1,2-addition products are formed initially when the cyclohexadienone carbene is reacted with the multiple bonds of conjugated dienes, which are isomerized under the conditions for the thermolysis of the quinone diazide, but are stable under photolysis conditions at 5–7°. 2. The rate of the thermal isomerization of the 1,2-addition products was studied.
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_________::9613cede5da00e882b301f18d5d7c9bc https://doi.org/10.1007/bf00924683 Zobrazit plný text záznamu Full text from SpringerLink