Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Marianne Vialemaringe"'
Publikováno v:
Canadian Journal of Chemistry. 79:257-262
The decomposition of allylic peroxides in methyl thioglycolate always leads to both epoxide and adduct peroxide. According to the nature of the allylic chain, either epoxide or peroxide is the predominant product, if not the only one. It is the first
Publikováno v:
Tetrahedron Letters. 41:4901-4904
Functional pinocarveols and bifunctional spiropinanes could be prepared by basic isomerisation of 2,3-epoxypinanes bearing a function or a functional chain on the carbone 10. Preliminary results are presented, which illustrate a general synthesis of
Publikováno v:
Helvetica Chimica Acta. 83:616-629
Autor:
Isabelle Pianet, Bourgeois M, Bernard Barbe, Christian Courseille, Marianne Vialemaringe, Evelyne Montaudon
Publikováno v:
Magnetic Resonance in Chemistry. 38:785-788
Autor:
Marianne Vialemaringe, Monique Campagnole, Sébastien Navarre, M. J. Bourgeois, John S. Lomas, Evelyne Montaudon
Publikováno v:
Journal of the Chemical Society, Perkin Transactions 2. :2129-2134
Despite previous reports to the contrary, addition of methyl thioglycolate to β-pinene always leads to both pinane and p-menthene adducts, the proportion of the latter increasing with the reaction temperature. This is attributable to the substantial
Publikováno v:
Synthesis. 1999:1607-1612
Publikováno v:
Comptes Rendus de l'Académie des Sciences - Series IIC - Chemistry. 2:449-454
Resume Cet article concerne l'isomerisation du 2,3-epoxypinane en presence d'acides de Lewis. Les donnees bibliographiques sont tres divergentes: selon les auteurs et dans les memes conditions, le produit majoritaire, voire exclusif, est soit l'α-ca
Publikováno v:
ChemInform. 30
Publikováno v:
Canadian Journal of Chemistry. Mar2001, Vol. 79 Issue 3, p257-262. 6p.
Publikováno v:
Helvetica Chimica Acta; 2000, Vol. 83 Issue 3, p616-629, 14p