Zobrazeno 1 - 10
of 102
pro vyhledávání: '"J.-M. Surzur"'
Publikováno v:
ChemInform. 22
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2e660511911d4b9f9b184b4a8faf0dad
https://doi.org/10.1002/chin.199141138
https://doi.org/10.1002/chin.199141138
Publikováno v:
ChemInform. 24
The sulfonyl radical-promoted cyclizations of 1,6-unsymmetrical dienes can be totally chemoselective. The addition of tosyl halides to various 1,6-dienes bearing both a nucleophilic and an electrophilic double bond clearly indicates that the attracti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::508ba3559c9e95aa7085c77258577c1f
https://doi.org/10.1002/chin.199310093
https://doi.org/10.1002/chin.199310093
Publikováno v:
The Journal of Organic Chemistry. 57:6118-6125
The sulfonyl radical-promoted cyclizations of 1,6-unsymmetrical dienes can be totally chemoselective. The addition of tosyl halides to various 1,6-dienes bearing both a nucleophilic and an electrophilic double bond clearly indicates that the attracti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::823abb0dff116316c160b5812f7424a9
https://doi.org/10.1021/jo00049a014
https://doi.org/10.1021/jo00049a014
Publikováno v:
Tetrahedron. 46:5285-5294
Addition of TsBr to diallyl malonates and allyl methallyl malonates is described. These cyclization reactions exhibit high stereoselectivity and very high regioselectivity. The structure of the reaction products is elucidated using 2D NMR.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d81b66c9dcc1e76e3efc9eafc71d83dd
https://doi.org/10.1016/s0040-4020(01)87835-2
https://doi.org/10.1016/s0040-4020(01)87835-2
Publikováno v:
ChemInform. 21
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9895fa0f528c30ab8deae113da1bcbf6
https://doi.org/10.1002/chin.199048104
https://doi.org/10.1002/chin.199048104
Publikováno v:
ChemInform. 21
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d8e2ebc8d52484da766b65776fe6253b
https://doi.org/10.1002/chin.199019169
https://doi.org/10.1002/chin.199019169
Publikováno v:
Tetrahedron. 37:2843-2854
Resume On decrit la synthese d'aryl-3 hexene-5 yl amines et les cyclisations des N-chloroamines correspondantes. Lorsque les reactions de cyclisation se font par addition de radicaux aminyle sur les doubles liaisons ethyleniques on obtient des phenyl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5d21ee2c39d23d704b5838943d544df9
https://doi.org/10.1016/s0040-4020(01)92354-3
https://doi.org/10.1016/s0040-4020(01)92354-3
Autor:
J.-M. Surzur, Lucien Stella
Publikováno v:
Tetrahedron Letters. 15:2191-2194
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f2dc662770a917c0f695f6ee326189e0
https://doi.org/10.1016/s0040-4039(01)93173-9
https://doi.org/10.1016/s0040-4039(01)93173-9
Publikováno v:
Tetrahedron Letters. 26:1209-1212
Ag (I) mediated persulphate oxidation of various 2-methyl benzoic acids and acrylic acids, co-catalyzed by Cu (II), leads to unsaturated γ-lactones, together with decarboxylation products. Lactonisation proceeds through 1,5 hydrogen transfer from in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e03fa9261318b42f77524e0ce8f6e7e4
https://doi.org/10.1016/s0040-4039(00)98435-1
https://doi.org/10.1016/s0040-4039(00)98435-1
Publikováno v:
Tetrahedron Letters. 23:5039-5042
Several β-aminothiols prepared from 3-piperideine and different thiiranes react by free radical reactio chemically initiated to yield exclusively 7-thia-1-azabicyclo (4,3,0) nonane derivatives. Even when this process is in competition with a radical
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d19f1398d183d2e1773602b8c447895a
https://doi.org/10.1016/s0040-4039(00)85567-7
https://doi.org/10.1016/s0040-4039(00)85567-7