Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Galantay Eugene E"'
Autor:
J. H. Trapold, Nicholas Paolella, L. C. Iorio, George Leslie, John H. Gogerty, Clarence Hoffman, Galantay Eugene E
Publikováno v:
Journal of Medicinal Chemistry. 12:444-449
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::698e4e29151366d248ef9a316fad5400
https://doi.org/10.1021/jm00303a025
https://doi.org/10.1021/jm00303a025
Publikováno v:
Journal of the American Chemical Society. 92:5771-5773
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::15ccf664e755577663d1518c6ec4bec7
https://doi.org/10.1021/ja00722a058
https://doi.org/10.1021/ja00722a058
Publikováno v:
Journal of the American Chemical Society. 88:3875-3877
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::06cfc2ebd7d8aa14dba9520ec5cf68d0
https://doi.org/10.1021/ja00968a047
https://doi.org/10.1021/ja00968a047
Autor:
Max Denzer, L. C. Iorio, R. J. Strohschein, G. Corriveau, Galantay Eugene E, R. Simpson, Ryan Ea, Douglas C. Knorr, N. A. Paodella, John H. Gogerty, Y. Uike
Publikováno v:
Chemischer Informationsdienst. 6
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e33ec01e30c2d3e7df696798d810fd7b
https://doi.org/10.1002/chin.197515250
https://doi.org/10.1002/chin.197515250
Publikováno v:
Chemischer Informationsdienst. Organische Chemie. 1
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::23b585c15cbe1b974f4e77ed78a01911
https://doi.org/10.1002/chin.197049386
https://doi.org/10.1002/chin.197049386
Publikováno v:
Chemischer Informationsdienst. Organische Chemie. 2
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::42ff83c9eb8c89c64beef50c789e2da6
https://doi.org/10.1002/chin.197113303
https://doi.org/10.1002/chin.197113303
Publikováno v:
Journal of the Chemical Society D: Chemical Communications. :274
An apparently general, hitherto unobserved reaction pathway for α-oximino-ketones, mechanistically related to the Semmler–Wolff aromatization, is described and put in the framework of “non-Beckmannian reactions”; a novel explanation is suggest
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::445fa0e77e27f9ee348bdcbf821f1acd
https://doi.org/10.1039/c29700000274
https://doi.org/10.1039/c29700000274
Publikováno v:
Journal of the Chemical Society, Perkin Transactions 1. :2095
Alkylation of an 11-oxoestrone derivative (I) has been shown to give a 9α-methyl product which could be further transformed into 9α-methyl-19-nor-compounds. A 9β-methyl-11-oxoestrone has been converted into 9β-methylestrone 3-methyl ether and a s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f70550f9c6ed8f4f8327b6240bb07fe9
https://doi.org/10.1039/p19730002095
https://doi.org/10.1039/p19730002095