Zobrazeno 1 - 10
of 209
pro vyhledávání: '"J. F. NORMANT"'
Publikováno v:
Tetrahedron. 49:7679-7690
Resume Les etats de transition de differents processus thermiques (elimination, rearrangement sigmatropique) ont ete evalues par la methode AM1. Le processus de rearrangement sigmatropique est le plus favorise et l'etat de transition bateau est plus
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ccf01ad3905e2b7dfe101b5fc3dc11e9
https://doi.org/10.1016/s0040-4020(01)87243-4
https://doi.org/10.1016/s0040-4020(01)87243-4
Autor:
J.-F. Normant
Publikováno v:
ChemInform. 22
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7d5dec9446041c2be43f8296f6536f35
https://doi.org/10.1002/chin.199113305
https://doi.org/10.1002/chin.199113305
Autor:
J. F. Normant
Publikováno v:
ChemInform. 22
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b3201c5ad6e9a3abe74a1edc6ed2a7b6
https://doi.org/10.1002/chin.199108371
https://doi.org/10.1002/chin.199108371
Autor:
J.‐F. Normant, R. Sauvetre
Publikováno v:
ChemInform. 22
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3ddeec5476ed9f1c3ec8df9886922873
https://doi.org/10.1002/chin.199152132
https://doi.org/10.1002/chin.199152132
Autor:
J. F. Normant
Publikováno v:
ChemInform. 23
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::23d15ff175b8cc60e710457c56c8eb2c
https://doi.org/10.1002/chin.199219344
https://doi.org/10.1002/chin.199219344
Publikováno v:
ChemInform. 25
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::24022121ea4562133424564f91df3d11
https://doi.org/10.1002/chin.199451117
https://doi.org/10.1002/chin.199451117
Autor:
J.-F. Normant
Publikováno v:
ChemInform. 27
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4fe3dfc5451f777b7f4aa6b7d9578095
https://doi.org/10.1002/chin.199627312
https://doi.org/10.1002/chin.199627312
Publikováno v:
ChemInform. 27
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6aac01fa81b331692014bff36f5974d8
https://doi.org/10.1002/chin.199652193
https://doi.org/10.1002/chin.199652193
Publikováno v:
Tetrahedron: Asymmetry. 2:223-230
The asymmetric epoxidation of an α,β-difluoro primary allylic alcohol, and of two α-fluoro secondary allylic alcohols follows the pattern known with non fluorinated analogs. The fluoro epoxides thus formed can be transformed into chiral α-ketols
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::550f8aec29a9fdac1191c3e3fcc4b6c7
https://doi.org/10.1016/s0957-4166(00)82361-7
https://doi.org/10.1016/s0957-4166(00)82361-7