Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Lycia Uttaro"'
Autor:
Véronique Barragan-Montero, Catalina Gurgui-Ionescu, Loïc Toupet, Alain Fruchier, Lycia Uttaro
Publikováno v:
Tetrahedron
Tetrahedron, Elsevier, 2007, 63, pp.9345-9353. ⟨10.1016/j.tet.2007.07.002⟩
Tetrahedron, 2007, 63, pp.9345-9353. ⟨10.1016/j.tet.2007.07.002⟩
Tetrahedron, Elsevier, 2007, 63, pp.9345-9353. ⟨10.1016/j.tet.2007.07.002⟩
Tetrahedron, 2007, 63, pp.9345-9353. ⟨10.1016/j.tet.2007.07.002⟩
International audience; A comparative study of the Mitsunobu reaction at C1 and C6 positions of mannose using bis(2,2,2-trifluoroethyl) malonate as nucleophile is disclosed. While C-alkylation was predominant at the C6 position, only O-alkylation occ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::82aef2c4012c7dbdad09d71f750da79e
https://doi.org/10.1016/j.tet.2007.07.002
https://doi.org/10.1016/j.tet.2007.07.002
Autor:
Patrick Rollin, Lycia Uttaro, Arnaud Tatibouët, Jean-Pierre Uttaro, Christophe Mathé, Christian Périgaud
Publikováno v:
Tetrahedron Letters
Tetrahedron Letters, Elsevier, 2007, 48, pp.3851-3854. ⟨10.1016/j.tetlet.2007.03.153⟩
Tetrahedron Letters, Elsevier, 2007, 48, pp.3851-3854. ⟨10.1016/j.tetlet.2007.03.153⟩
The use of phenylsulfonylethylidene (PSE) acetal as a new 3′,5′-bridged protecting group in nucleoside chemistry is reported. The PSE acetal demonstrates to be compatible with Lewis acids used in standard glycosylation reactions. In addition, a s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::22a6fb4a8968085b46165520e6a13d67
https://hal.archives-ouvertes.fr/hal-00159598
https://hal.archives-ouvertes.fr/hal-00159598
