Zobrazeno 1 - 10
of 48
pro vyhledávání: '"Evelyne Montaudon"'
Publikováno v:
Bulletin des Sociétés Chimiques Belges. 89:1039-1042
Acetonyl radicals created by action of di-t-butylperoxide on acetone (molar ratios acetone/acetylenic compound/DTBP = 20/1/0.2; 150°C; 3h) add to acetylenic compounds and lead to the formation of 1/1 adducts in low to moderate yields. 2/1 adducts ar
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9577d15a33d1cf81333ad747d574f9fd
https://doi.org/10.1002/bscb.19800891203
https://doi.org/10.1002/bscb.19800891203
Publikováno v:
Bulletin des Sociétés Chimiques Belges. 88:677-682
Addition of acetonyl radicals to 1-octyne leads to the formation of 1/1 adducts. Besides the normal product, appear two kinds of cyclic derivatives. Formation of the latter is explained by hydrogen shifts in the transient vinyl radical. 1,5-hydrogen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::de9819968180a89a3a078585dec83258
https://doi.org/10.1002/bscb.19790880907
https://doi.org/10.1002/bscb.19790880907
Publikováno v:
Bulletin des Sociétés Chimiques Belges. 97:255-262
Thermolyses of dicyclohexyl carbonyl peroxide have been performed in organic solutions of t-butyl pent-4-enyl peroxide or t-butyl perpent-4-enoate in order to study the induced decomposition by cyclohexyl radicals of these peroxides. Induced decompos
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1e96c63cbf6e2451a35f701e5b1f9f0a
https://doi.org/10.1002/bscb.19880970403
https://doi.org/10.1002/bscb.19880970403
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
Publikováno v:
Bulletin des Sociétés Chimiques Belges. 96:769-774
Free radical additions of cyclohexane, tetrahydrofuran, methyl propanoate, acetonitrile, dichloromethane to allyl t-butyl peroxide, t-butyl 2-methyl prop-2-enyl peroxide, t-butyl 2,2-dimethyl prop-2-enyl peroxide and t-butyl 3-methyl but-2-enyl perox
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::359c13fc50877193baf8f1ddfecd8b1e
https://doi.org/10.1002/bscb.19870961007
https://doi.org/10.1002/bscb.19870961007
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
Autor:
Evelyne Montaudon, M. J. Bourgeois
Publikováno v:
Helvetica Chimica Acta. 84:2430-2438
Base-Induced Reactions of p-Menthane- and Pinane-Derived Epoxyesters – Coconut Fragrance The base-induced isomerization of p-menthane- and pinane-derived epoxy esters was studied. The reaction is dependent on the structure of the terpene compound,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1a5e5e834443f5870e89be67202509db
https://doi.org/10.1002/1522-2675(20010815)84:8<2430::aid-hlca2430>3.0.co
https://doi.org/10.1002/1522-2675(20010815)84:8<2430::aid-hlca2430>3.0.co
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