Zobrazeno 1 - 10
of 23
pro vyhledávání: '"E. BAGGIOLINI"'
Publikováno v:
Journal of the American Chemical Society. 92:4906-4921
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a3aac74a6101c09a5f4c4e9a1e773952
https://doi.org/10.1021/ja00719a026
https://doi.org/10.1021/ja00719a026
Publikováno v:
Helvetica Chimica Acta. 54:429-449
On ultraviolet irradiation O-acetyljervine (1) is subjected to several parallel fragmentations. From the complex reaction mixtures obtained in a variety of solvents (dioxan, tetrahydrofuran, acetonitrile, iso-octane, benzene) the major alicyclic prod
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6af88219ec4f307971f2f8f30def197f
https://doi.org/10.1002/hlca.19710540202
https://doi.org/10.1002/hlca.19710540202
Publikováno v:
Helvetica Chimica Acta. 50:297-306
In boiling xylene the cyclopentadienedione 1 is thermally decarbonylated to cis-8,9-dihydroindenone (8). This method avoids secondary reactions and allows the preparation of 8 in high yield.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e63546c9e977246295f136386bd42452
https://doi.org/10.1002/hlca.19670500137
https://doi.org/10.1002/hlca.19670500137
Autor:
A J Szuna, A C Loh, F J Leinweber, Gino J. Sasso, J. Triscari, Thomas H. Williams, E. Baggiolini, I. Bekersky
Publikováno v:
Xenobiotica; the fate of foreign compounds in biological systems. 17(12)
1. In 24 h, male rats excreted in urine 1% of an intra-gastric 100 mg/kg dose of 4-amino-5-ethyl-3-[4-14C]thiophenecarboxylic acid methyl ester hydrochloride (I) as unchanged I and 59% as 4-amino-5-ethyl-3-thiophenecarboxylic acid (II), mostly conjug
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::62cbd4730771286b7301dbb46849f148
https://pubmed.ncbi.nlm.nih.gov/3439191
https://pubmed.ncbi.nlm.nih.gov/3439191
Publikováno v:
Chemischer Informationsdienst. 6
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a9f02a4877aa76c8e53e8c20d20eb496
https://doi.org/10.1002/chin.197517474
https://doi.org/10.1002/chin.197517474
Publikováno v:
Chemischer Informationsdienst. 13
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f7628b27f25d7ca3bf74649292ddda1b
https://doi.org/10.1002/chin.198216209
https://doi.org/10.1002/chin.198216209
Publikováno v:
Chemischer Informationsdienst. Organische Chemie. 1
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::46923c14d30166007104cdd7178b63b7
https://doi.org/10.1002/chin.197044166
https://doi.org/10.1002/chin.197044166
Publikováno v:
Chemischer Informationsdienst. Organische Chemie. 2
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::59f440b66d365b67778e33a68a9e207b
https://doi.org/10.1002/chin.197119286
https://doi.org/10.1002/chin.197119286
Publikováno v:
J. Chem. Soc. D. :1103-1104
In solution, 3-acetyl-1,2,3-trimethylcyclopent-1-ene (I) undergoes a sigmatropic 1,3-acetyl shift as the major unimolecular reaction in the excited singlet state, and a (thermatically reversible) 1,2-acetyl shift with cyclopropane ring-closure as the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f9911ba8146f49d272b6ccf3b6b484d7
https://doi.org/10.1039/c29690001103
https://doi.org/10.1039/c29690001103