Zobrazeno 1 - 10
of 10
pro vyhledávání: '"P. J. Karnik"'
Publikováno v:
European Journal of Medicinal Chemistry. 31:485-488
Summary Various substituted diphenyl bisamidines were prepared and tested for antiamoebic activity in Golden hamsters and Wistar rats. Compounds 10 showed in vitro activity at 100 μg/mL and displayed excellent in vivo activity against hepatic infect
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::33a6f898addbb1df542eb8f6e9e6f270
https://doi.org/10.1016/0223-5234(96)85169-5
https://doi.org/10.1016/0223-5234(96)85169-5
Publikováno v:
European Journal of Medicinal Chemistry. 30:697-706
Summary Various ethers and thioethers of dihydroartemisinin were prepared by treating dihydroartemisinin with hydroxy alkyl, substituted phenol, hydroxy aralkyl, hydroxy alkynyl and hydroxy heteroalkyl or thiols in the presence of BF3Et2O. The thioet
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f147502086f32ff23e0549c15c854ea5
https://doi.org/10.1016/0223-5234(96)88287-0
https://doi.org/10.1016/0223-5234(96)88287-0
Publikováno v:
Tetrahedron Letters. 34:6305-6308
Refluxing the propargyl ether 2c with nBu 3 SnH/AIBN in toluene gave the clean single stereoisomer 3 . Similarly the other isomer 2d underwent a smooth radical cyclisation to give 5 . The allyl ether 2e gave 6 , a 1,2-cia 1,5-trans product, under sim
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::96f3c9fe13ac1c359677d5e21983a52b
https://doi.org/10.1016/s0040-4039(00)73738-5
https://doi.org/10.1016/s0040-4039(00)73738-5
Publikováno v:
ChemInform. 22
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::52bf9b87bbe6343dad384901ea6591b9
https://doi.org/10.1002/chin.199141175
https://doi.org/10.1002/chin.199141175
Publikováno v:
ChemInform. 25
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ef8fa32d18b80ca5ac9ffecf63f88e6c
https://doi.org/10.1002/chin.199414261
https://doi.org/10.1002/chin.199414261
Publikováno v:
ChemInform. 25
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9e3b9124dcc02e64acc47ca6dc0dbb48
https://doi.org/10.1002/chin.199452144
https://doi.org/10.1002/chin.199452144
Publikováno v:
ChemInform. 27
Summary Various ethers and thioethers of dihydroartemisinin were prepared by treating dihydroartemisinin with hydroxy alkyl, substituted phenol, hydroxy aralkyl, hydroxy alkynyl and hydroxy heteroalkyl or thiols in the presence of BF3Et2O. The thioet
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f0927569677b8e011a9c4665bf478cf5
https://doi.org/10.1002/chin.199602235
https://doi.org/10.1002/chin.199602235
Publikováno v:
ChemInform. 27
Heating the propynyldihydroartemisinin derivatives 4 and 5 with Bu3SnH–AIBN in toluene gave the stereoisomers 18 and 20 (5-exo trig products) respectively. The allyl ether 6 gave 21, a 1,2-cis 1,5-trans product under similar conditions, whereas the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4b33d9492a1edf4733fded27777daab7
https://doi.org/10.1002/chin.199634201
https://doi.org/10.1002/chin.199634201
Publikováno v:
ChemInform. 21
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1d3862bcc1890c18c0facbe7bd855cd1
https://doi.org/10.1002/chin.199030089
https://doi.org/10.1002/chin.199030089
Publikováno v:
ChemInform. 19
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::680b0b1132fbf936bcf8a21bfd889343
https://doi.org/10.1002/chin.198820193
https://doi.org/10.1002/chin.198820193