Zobrazeno 1 - 10
of 28
pro vyhledávání: '"Monique Campagnole"'
Publikováno v:
Bulletin des Sociétés Chimiques Belges. 91:725-728
The reaction of N,N′-carbonyldiimidazole with but-3 enoic acid did not lead to the expected azolide; its rearrangement into conjugated isomer was followed by imidazole addition to the double bond. These two reactions make inefficient this preparati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::93eb43630dceaabc75d00332c8678734
https://doi.org/10.1002/bscb.19820910808
https://doi.org/10.1002/bscb.19820910808
Autor:
Monique Campagnole, Bernard Delmond
Publikováno v:
Synthetic Communications. 37:1077-1090
β‐Damascenone and β‐damascone derivatives, important fragrant compounds, were directly obtained from β‐ionone by a new way via retro‐α‐ionol.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6ebdfa4ff9b2118509dd704237b2b0b4
https://doi.org/10.1080/00397910701196546
https://doi.org/10.1080/00397910701196546
Publikováno v:
Tetrahedron. 58:1165-1171
Resume La photooxygenation des γ- et δ-pyronenes, realisee pour la premiere fois, conduit classiquement a un hydroperoxyde, un hydroperoxy-peroxyde, et un endoperoxyde respectivement. La reactivite de ces peroxydes est etudiee. Ils conduisent a des
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7418883b81e4007d4fd35851006da108
https://doi.org/10.1016/s0040-4020(01)01211-x
https://doi.org/10.1016/s0040-4020(01)01211-x
Publikováno v:
Synthesis. 2001:1883-1887
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::35b3e6aac572a5e7100669bec3a68466
https://doi.org/10.1055/s-2001-17530
https://doi.org/10.1055/s-2001-17530
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7f08db1c933ec06f7727ba8e83e920d7
https://doi.org/10.1139/cjc-79-3-257
https://doi.org/10.1139/cjc-79-3-257
Publikováno v:
Bulletin des Sociétés Chimiques Belges. 100:93-95
Une synthese de peroxydes allyliques dissymetriques est decrite a partier des mesylates convenables. La nature du solvant est un facteur determinant de la regioselectivite de la reaction.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dac81d1d6395de802b4194c92ef49d33
https://doi.org/10.1002/bscb.19911000113
https://doi.org/10.1002/bscb.19911000113
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d8606696ff2e0879554ebc2d8fd7efa9
https://doi.org/10.1016/s0040-4039(00)00757-7
https://doi.org/10.1016/s0040-4039(00)00757-7
Publikováno v:
Helvetica Chimica Acta. 83:616-629
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6b65c126d442bd401d94613fa43c3268
https://doi.org/10.1002/(sici)1522-2675(20000315)83:3<616::aid-hlca616>3.0.co
https://doi.org/10.1002/(sici)1522-2675(20000315)83:3<616::aid-hlca616>3.0.co
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7ba1c576449234b1d9afe3ad868918c7
https://doi.org/10.1039/b002854l
https://doi.org/10.1039/b002854l
Publikováno v:
Synthesis. 1999:1607-1612
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::80f2f2dc5c4e7e9421ae0158e7ea1cdd
https://doi.org/10.1055/s-1999-3574
https://doi.org/10.1055/s-1999-3574