Zobrazeno 1 - 10
of 43
pro vyhledávání: '"G. Nathansohn"'
Publikováno v:
Tetrahedron Letters. 20:2921-2924
The title conversion was achieved by condensation of 2-Amino-2,3-dihydro-1H-isoindol 1-one with ethyl benzoyl or aceto/acetate followed by base-promoted rearrangement.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f65be2243af93055e353ad330d796757
https://doi.org/10.1016/s0040-4039(01)86453-4
https://doi.org/10.1016/s0040-4039(01)86453-4
Publikováno v:
Tetrahedron Letters. 17:111-114
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::16bda0e3eb612d68772cdd88d2a7a826
https://doi.org/10.1016/s0040-4039(00)93034-x
https://doi.org/10.1016/s0040-4039(00)93034-x
Publikováno v:
The Journal of Organic Chemistry. 27:3677-3680
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8cb54d42ea2a099e2905e2067329596d
https://doi.org/10.1021/jo01057a503
https://doi.org/10.1021/jo01057a503
Publikováno v:
Steroids. 5:263-277
Dehydroepiandrosterone (3β-hydroxyandrost-5-en-17-one) and 3 β-hydroxy-5α-androstan-17-one was converted by Bucherer synthesis to an isomeric pair of 17-spiro-hydantoins. The hydantoins were split by alkaline hydrolysis into 17-amino-17-carboxylic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::32762385b2f30fd7ae25bcc051c0673e
https://doi.org/10.1016/0039-128x(65)90138-8
https://doi.org/10.1016/0039-128x(65)90138-8
Publikováno v:
Steroids. 13:365-381
The pharmacological data related to the neoglycogenetic and antinflammatory activity of a new series of [17α,16α-d]-oxazolino analogs of corticosteroids are reported. The substituent in the 2'-position of the oxazoline nucleus has a decisive influe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b8aa1379e3cbc04cb24f944c691c32d5
https://doi.org/10.1016/0039-128x(69)90045-2
https://doi.org/10.1016/0039-128x(69)90045-2
Publikováno v:
Il Farmaco; edizione scientifica. 30(6)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::96af673b981d7e58e2bbc166ffa285c5
https://pubmed.ncbi.nlm.nih.gov/1140380
https://pubmed.ncbi.nlm.nih.gov/1140380
Publikováno v:
Chemischer Informationsdienst. 6
The synthesis is described of a number of 3-aminopyrazolo[1,2-b]phthalazine-1(1H),5(10H)-diones (I) differently substituted on the amino group and in position 2, through condensation of alpha-chloro-beta-chlorocarbonylenamines (IV) with the 3,4-dihyd
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::da1d0463f8b7f57fbd05804da06d540f
https://doi.org/10.1002/chin.197546300
https://doi.org/10.1002/chin.197546300
Autor:
G, Nathansohn, G, Winters
Publikováno v:
Advances in experimental medicine and biology. 171
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::3c29a172bb288af9cac52937ec295126
https://pubmed.ncbi.nlm.nih.gov/6372389
https://pubmed.ncbi.nlm.nih.gov/6372389
Publikováno v:
Il Farmaco; edizione scientifica. 30(08)
The synthesis is described of a number of 3-aminopyrazolo[1,2-b]phthalazine-1(1H),5(10H)-diones (I) differently substituted on the amino group and in position 2, through condensation of alpha-chloro-beta-chlorocarbonylenamines (IV) with the 3,4-dihyd
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::494f15cfde031a71b7f1559618b0361f
https://pubmed.ncbi.nlm.nih.gov/1149874
https://pubmed.ncbi.nlm.nih.gov/1149874
Publikováno v:
Chemischer Informationsdienst. 6
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6bdaba8a191e9880ab8d1914b0fe9446
https://doi.org/10.1002/chin.197522308
https://doi.org/10.1002/chin.197522308