Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Manfre, Franco"'
Autor:
Manfre, Franco
Th. univ.--Chim. org.--Strasbourg 1, 1988.
Externí odkaz:
http://catalogue.bnf.fr/ark:/12148/cb37615714d
Autor:
Carrell, H. L., Glusker, Jenny P., Burger, Vincent, Manfre, Franco, Tritsch, Denis, Biellmann, Jean-Francois
Publikováno v:
Proceedings of the National Academy of Sciences of the United States of America, 1989 Jun . 86(12), 4440-4444.
Externí odkaz:
https://www.jstor.org/stable/33706
Publikováno v:
Synthetic Communications. 27:425-430
2-(4-Chlorophenyl)propanoic acid 1 is transformed to 2-(4-chloro-3-nitrophenyl) propanoic acid 2 (94% yield). Acid 2 can be converted to 2-(3-nitrophenyl)propanoic acid 3 (70% yield) or to 2-(3-aminophenyl) propanoic acid 4 (80% yield).
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3e84de84b9dc81bfb5d33e22232170ff
https://doi.org/10.1080/00397919708006043
https://doi.org/10.1080/00397919708006043
Autor:
J. P. Pulicani, Manfre Franco
Publikováno v:
Tetrahedron: Asymmetry. 5:235-238
Pyrrolidine derivatives have been identified as a new class of non-peptide CCK antagonists. Enantiomers of RP 66803 , a representative compound of this chemical family were previously prepared by chiral chromatography of the racemate. In order to det
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::240518071264643ae363e8221b06f57f
https://doi.org/10.1016/s0957-4166(00)86178-9
https://doi.org/10.1016/s0957-4166(00)86178-9
Autor:
J. P. Pulicani, Manfre Franco
Publikováno v:
ChemInform. 25
Pyrrolidine derivatives have been identified as a new class of non-peptide CCK antagonists. Enantiomers of RP 66803 , a representative compound of this chemical family were previously prepared by chiral chromatography of the racemate. In order to det
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f6a16832f5d7815b2fac092d36c5a604
https://doi.org/10.1002/chin.199428295
https://doi.org/10.1002/chin.199428295
Publikováno v:
ChemInform. 28
2-(4-Chlorophenyl)propanoic acid 1 is transformed to 2-(4-chloro-3-nitrophenyl) propanoic acid 2 (94% yield). Acid 2 can be converted to 2-(3-nitrophenyl)propanoic acid 3 (70% yield) or to 2-(3-aminophenyl) propanoic acid 4 (80% yield).
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f9deb6db8c8a36785dac0de6ef1131a7
https://doi.org/10.1002/chin.199725078
https://doi.org/10.1002/chin.199725078
Autor:
Jimonet, Patrick, Bohme, Georg Andrees, Bouquerel, Jean, Boireau, Alain, Damour, Dominique, Debono, Marc Williams, Genevois-Borella, Arielle, Hardy, Jean-Claude, Hubert, Philippe, Manfré, Franco, Nemecek, Patrick, Pratt, Jeremy, Randle, John C.R., Ribeill, Yves, Stutzmann, Jean-Marie, Vuilhorgne, Marc, Mignani, Serge
Publikováno v:
In Bioorganic & Medicinal Chemistry Letters January 2001 11(2):127-132
Autor:
Manfre, Franco1 franco.manfre@minasolve.com, Patouillard, Norbert2
Publikováno v:
Speciality Chemicals. Mar2015, Vol. 35 Issue 3, p12-13. 2p.
Autor:
Manfré, Franco, Pulicani, Jean Pierre
Publikováno v:
In Tetrahedron: Asymmetry 1994 5(2):235-238