Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Priscille Devin"'
Autor:
José Marco-Contelles, Juliana Ruiz-Caro, Emily Mainetti, Max Malacria, Louis Fensterbank, Priscille Devin
Publikováno v:
Tetrahedron. 58:1147-1158
The intramolecular Pauson–Khand (PK) reaction of 4-bromomethyldimethylsilyloxy-4-ethynyl-6,6-dimethyloct-1-en-7-yne ( 1 ), the differently functionalized 4-ethynyl-octa-1,7-dienes ( 2–6 ), and 5-ethynyl-5-hydroxy-2,4,4-trimethyl-nona-1,8-diene (
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::712641aa7071899fe50c49bd7075fa31
https://doi.org/10.1016/s0040-4020(01)01209-1
https://doi.org/10.1016/s0040-4020(01)01209-1
Publikováno v:
Tetrahedron Letters. 40:5511-5514
The radical cyclization of several ω-iodoaldehydes and a ketone can be accomplished without the use of tributyltin hydride. Triethylborane in presence of oxygen or light from a sun lamp can serve as a radical initiator and terminator. In these condi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e1e33c2d1817893162fbebe3f01baa7d
https://doi.org/10.1016/s0040-4039(99)01072-2
https://doi.org/10.1016/s0040-4039(99)01072-2
Publikováno v:
Tetrahedron Letters. 39:833-836
The reaction of aldehydes 1 and 10 with Bu 3 SnH has been studied. In thermal conditions, after an initial chemoselective 6- exo-trig or 5- exo-trig cyclization to the aldehyde, a β-scission reaction takes place, providing rearrangement products. At
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7b5dfcbcd6d0ecc9ab35dd3742dcfc45
https://doi.org/10.1016/s0040-4039(97)10743-2
https://doi.org/10.1016/s0040-4039(97)10743-2
Publikováno v:
ChemInform. 29
The reaction of aldehydes 1 and 10 with Bu 3 SnH has been studied. In thermal conditions, after an initial chemoselective 6- exo-trig or 5- exo-trig cyclization to the aldehyde, a β-scission reaction takes place, providing rearrangement products. At
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c65715838033664518ee1c15fe7fd43d
https://doi.org/10.1002/chin.199819044
https://doi.org/10.1002/chin.199819044
Autor:
Louis Fensterbank, Emmanuel Lacôte, Priscille Devin, Max Malacria, Stephane L. Bogen, Michel Journet
Publikováno v:
ChemInform. 30
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6d35e0bea668968760dcf3a3e36d8961
https://doi.org/10.1002/chin.199923347
https://doi.org/10.1002/chin.199923347
Publikováno v:
ChemInform. 30
The radical cyclization of several ω-iodoaldehydes and a ketone can be accomplished without the use of tributyltin hydride. Triethylborane in presence of oxygen or light from a sun lamp can serve as a radical initiator and terminator. In these condi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dd720dfe63cea5b28739a41f347c5425
https://doi.org/10.1002/chin.199944085
https://doi.org/10.1002/chin.199944085
Publikováno v:
ChemInform. 31
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fa16ab3cef34f2ab2abfeec1ddb62da7
https://doi.org/10.1002/chin.200017044
https://doi.org/10.1002/chin.200017044
Publikováno v:
Synlett. 2000:83-85
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1ca0b90ab9f6c7c1a8c0ad50e4b7f030
https://doi.org/10.1055/s-2000-6438
https://doi.org/10.1055/s-2000-6438
Publikováno v:
Synlett. 2000:1342-1344
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7a50a46cf3f5755b79b08d950f6d710f
https://doi.org/10.1055/s-2000-7139
https://doi.org/10.1055/s-2000-7139
Autor:
Max Malacria, Louis Fensterbank, Anne-Lise Dhimane, Matthew L. Maddess, Youssef Harrak, Célia Brancour, Priscille Devin, Emily Mainetti
Publikováno v:
ChemInform. 38
Radical cascades employing (dichloromethyl)dimethylsilyl ethers as both a point of radical initiation and termination, allow efficient entry to fused polycyclic cyclopropanes, and are also suitable for the design of other radical processes terminated
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9a684ffe833167e38f1eb3ae7f03f72d
https://doi.org/10.1002/chin.200728065
https://doi.org/10.1002/chin.200728065