Zobrazeno 1 - 10
of 48
pro vyhledávání: '"Francis Barbot"'
Publikováno v:
Tetrahedron. 65:10105-10123
The synthesis of azobenzene derivatives and of azo-linked carbohydrate moieties is reviewed. The report contains 119 references. Figure options Download full-size image Download as PowerPoint slide
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::46860ed595290afde98056be2cdd6a10
https://doi.org/10.1016/j.tet.2009.08.063
https://doi.org/10.1016/j.tet.2009.08.063
Publikováno v:
Organic Letters. 5:4915-4918
The microwave-assisted intramolecular [3 + 2] cycloaddition reaction of azomethine ylides to activated and nonactivated alkenes and alkynes is described. The procedure allows the synthesis of pyrrolidines and pyrrole products in good to excellent ove
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8e15a90706f0dedf8c838bbb6664d1e0
https://doi.org/10.1021/ol0361195
https://doi.org/10.1021/ol0361195
Publikováno v:
Synthetic Communications. 28:3279-3289
The reaction between Grignard reagents prepared from allylic or propargylic halides and the N-phenylsulfenimine derived from the heptane-2,6-dione affords primary 1-alkenyl (or alkynyl)-3-methylcyclohex-2-enamines in good yields.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a9f4c6b54460d178ffc7e512ca6002ee
https://doi.org/10.1080/00397919808004433
https://doi.org/10.1080/00397919808004433
Autor:
Francis Barbot, Léone Miginiac
Publikováno v:
Synthetic Communications. 27:2601-2614
Reaction of N-unsubstituted ketimines with organoaluminum reagents prepared from allylic and propargylic halides, allows to prepare, in good yields, tertiary carbinamines with three different groups (phenyl, alkyl and α-unsaturated group) on the ter
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cff858d4f471c941dc41d764130f3652
https://doi.org/10.1080/00397919708004130
https://doi.org/10.1080/00397919708004130
Publikováno v:
Journal of Organometallic Chemistry. 534:117-127
A new general synthesis of C-subtituted α -aminoacids is described, using at first the regioselective reaction between α -unsaturated organozincs and N -(phenylsulfanyl)iminoesters.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8069ebc6bbec7842bd7f467e86cd5ce0
https://doi.org/10.1016/s0022-328x(96)06854-4
https://doi.org/10.1016/s0022-328x(96)06854-4
Publikováno v:
ChemInform. 22
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7091779e031297254d07374d708e7545
https://doi.org/10.1002/chin.199126135
https://doi.org/10.1002/chin.199126135
Publikováno v:
ChemInform. 22
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6f0cccecd1e8e64512190afdf675e72a
https://doi.org/10.1002/chin.199138090
https://doi.org/10.1002/chin.199138090
Autor:
Francis Barbot, Ph. Miginiac
Publikováno v:
ChemInform. 24
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5b95c6c7d6e8fa0f034c8e7fbf468c18
https://doi.org/10.1002/chin.199308150
https://doi.org/10.1002/chin.199308150
Autor:
Léone Miginiac, Francis Barbot
Publikováno v:
ChemInform. 28
Reaction of N-unsubstituted ketimines with organoaluminum reagents prepared from allylic and propargylic halides, allows to prepare, in good yields, tertiary carbinamines with three different groups (phenyl, alkyl and α-unsaturated group) on the ter
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::085a5651e4d057b726f0fc906c3a9497
https://doi.org/10.1002/chin.199742105
https://doi.org/10.1002/chin.199742105
Publikováno v:
ChemInform. 28
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f6aa8a8083fa6f2d4a44b10cfae7fdab
https://doi.org/10.1002/chin.199746092
https://doi.org/10.1002/chin.199746092