Zobrazeno 1 - 10
of 35
pro vyhledávání: '"G. Drutkowski"'
Publikováno v:
ChemInform. 33
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9a9c9961559b8fc001ef162a9654af51
https://doi.org/10.1002/chin.200226159
https://doi.org/10.1002/chin.200226159
Publikováno v:
ChemInform. 33
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3704107a3c3c2a16498ac2dad0876acc
https://doi.org/10.1002/chin.200231166
https://doi.org/10.1002/chin.200231166
Publikováno v:
ChemInform. 33
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9f38e2a4811567017c68193c9bd9151d
https://doi.org/10.1002/chin.200242168
https://doi.org/10.1002/chin.200242168
Publikováno v:
ChemInform. 35
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2defceee3e75ed07f0f96b5b412d0822
https://doi.org/10.1002/chin.200439130
https://doi.org/10.1002/chin.200439130
Publikováno v:
Die Pharmazie. 59(6)
pH-Dependant reduction of the methyl 3-(2-nitrophenyl)thiophene-2-carboxylate (3), obtained by Suzuki cross-coupling of the methyl 3-iodothiophene-2-carboxylate with 2-nitrophenyl boronic acid yields the cyclic hydroxamic acid 4 and the lactam 5, res
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::11c588848296eb598f5aed891abefbd4
https://pubmed.ncbi.nlm.nih.gov/15248457
https://pubmed.ncbi.nlm.nih.gov/15248457
Publikováno v:
ChemInform. 35
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::582454b64e14df4385b9e6f367852b02
https://doi.org/10.1002/chin.200418140
https://doi.org/10.1002/chin.200418140
Publikováno v:
ChemInform. 35
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::927c30ae64e52fc038a5b18c8dec7ab5
https://doi.org/10.1002/chin.200409127
https://doi.org/10.1002/chin.200409127
Publikováno v:
Die Pharmazie. 59(1)
The reaction of 2-nitrobenzaldehyde with methyl propiolate and ammonium acetate in acetic acid yields 2,6-dinor-nifedipine (1a) and the isomeric rac. 1,4-dihydropyridine (DHP) 1b. The DHP 1 are dehydrogenated both chemically and by anodic oxidation u
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::9ef4f1fa045bc0d947fc5d4da5003c5c
https://pubmed.ncbi.nlm.nih.gov/14964415
https://pubmed.ncbi.nlm.nih.gov/14964415
Publikováno v:
Die Pharmazie. 58(11)
Hydrolysis of the dienamine function of the dihydrobiphenyls 3 leads to a mixture of the tautomers 4A-C (NMR). The structures of the starting material 3a and the products 4cA and 4bC are confirmed by X-ray crystal analysis. The biphenyls 5 are formed
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::b5ac4b1c37705b4908765c0fee5a9099
https://pubmed.ncbi.nlm.nih.gov/14664331
https://pubmed.ncbi.nlm.nih.gov/14664331
Publikováno v:
ChemInform. 34
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::eeca75b99e089b47ced876a90ea11e59
https://doi.org/10.1002/chin.200346159
https://doi.org/10.1002/chin.200346159