The reaction of 8-amino-p-menthene derivatives with electrophiles


Autoria(s): Bernhardt, P. V.; Carman, R. M.; Derbyshire, R. P. C.
Data(s)

01/01/2004

Resumo

Attempts to ring-close the nitrogen atom of 8-amino-p-menth-1-ene and of N-substituted 8-amino-p-menth-1-enes onto the C1 - C2 double-bond carbons has led to a range of bicyclo[2.2.2] and bicyclo[3.2.1] products, together with the novel bicyclo[4.3.1]-1,3-oxazepine 9.

Identificador

http://espace.library.uq.edu.au/view/UQ:71947

Idioma(s)

eng

Publicador

CSIRO Publishing

Palavras-Chave #Chemistry, Multidisciplinary #Halogenated Terpenoids #Limonene Tetrabromide #Semiempirical Methods #Allylic Oxidation #Optimization #Cyclization #Parameters #Alcohols #Acetate #System #C1 #250301 Organic Chemical Synthesis #780103 Chemical sciences
Tipo

Journal Article