Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Mathias Domostoj"'
Autor:
Mathias Domostoj, André Mann, Camille-Georges Wermuth, Jean Suffert, Karin Briner, Christophe Morice
Publikováno v:
Tetrahedron Letters. 42:6499-6502
Two intramolecular routes were experimented to reach the hexahydrobenzofuro(2,3-c)pyridine platform: a Heck and a radical reaction. The radical route was applicable to all substrates, whereas the Heck route was of limited use. The key adducts were ob
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::91358bfa57effdb52da433f8451c3e33
https://doi.org/10.1016/s0040-4039(01)01191-1
https://doi.org/10.1016/s0040-4039(01)01191-1
Autor:
Christophe Morice, Jean Suffert, Karin Briner, Mathias Domostoj, André Mann, Camille-Georges Wermuth
Publikováno v:
ChemInform. 33
Two intramolecular routes were experimented to reach the hexahydrobenzofuro(2,3-c)pyridine platform: a Heck and a radical reaction. The radical route was applicable to all substrates, whereas the Heck route was of limited use. The key adducts were ob
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0cbe724bf5b05f2c0bf08ea25a9e88d1
https://doi.org/10.1002/chin.200202164
https://doi.org/10.1002/chin.200202164
Publikováno v:
Tetrahedron Letters
Tetrahedron Letters, Elsevier, 2006, 47, pp.2205-2208
Tetrahedron Letters, Elsevier, 2006, 47, pp.2205-2208
N-Activated 2-phenylazetidines were opened regioselectively at the benzylic carbon with various allylsilanes or propargylsilane in the presence of BF3·Et2O, providing amino olefins, precursors of biomolecules such as phenyl-homo-kainoids.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5d0c42595e42829033c1180a52600d36
https://hal.archives-ouvertes.fr/hal-00129851
https://hal.archives-ouvertes.fr/hal-00129851
