Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Berger Dan Maarten"'
Autor:
Berger Dan Maarten, Minu Dutia, Gary Harold Birnberg, Frenel Fils Demorin, Yanong D. Wang, Dennis Powell
Publikováno v:
Synthesis. 2003:1712-1716
The regioselective synthesis of compound 3, a potent Src kinase inhibitor is described. A key step in this synthesis is the regioselective thermal rearrangement of a substituted benzocyclobutene to provide a 2,3,6,7-tetrasubstituted naphthalene. An e
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e028bdafc16abeb21ed9d5dffc4ec34c
https://doi.org/10.1055/s-2003-40872
https://doi.org/10.1055/s-2003-40872
Autor:
Dennis Powell, Minu Dutia, Berger Dan Maarten, Frenel Fils Demorin, Jennifer Weber, Yuri Raifeld, Allan Wissner, Frank Boschelli
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 12:2989-2992
A series of substituted 4-anilino-7-phenyl-3-quinolinecarbonitriles has been prepared as Src kinase inhibitors. Optimal activity is observed with compounds that have basic amines attached via the para position of the 7-phenyl ring, and a hydrogen ato
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0d64d2b2961df7d8d53021c60efe9f7c
https://doi.org/10.1016/s0960-894x(02)00577-2
https://doi.org/10.1016/s0960-894x(02)00577-2
Publikováno v:
Helvetica Chimica Acta. 82:326-337
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::adf52c6602fe2be8357285fcf179fae3
https://doi.org/10.1002/(sici)1522-2675(19990310)82:3<326::aid-hlca326>3.0.co
https://doi.org/10.1002/(sici)1522-2675(19990310)82:3<326::aid-hlca326>3.0.co
Publikováno v:
Helvetica Chimica Acta. 81:1792-1802
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::85d4d6f0ffd8fc75244509fc79a5507e
https://doi.org/10.1002/(sici)1522-2675(19981007)81:10<1792::aid-hlca1792>3.0.co
https://doi.org/10.1002/(sici)1522-2675(19981007)81:10<1792::aid-hlca1792>3.0.co
Publikováno v:
Helvetica Chimica Acta. 79:192-202
Reaction of ‘Push-Pull’ Enynes with Acids. First Observation of a Rearrangement of 5-Chloro-5-(dialkylamino)pentadienals ‘Push-pull’-enynes 7 react easily with HCl as well as with AcOH to give 5-amino-5-chloropentadienals 8 and 5-(acetoxy)-5-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::71806126a2015582ccfd99ecaa414937
https://doi.org/10.1002/hlca.19960790119
https://doi.org/10.1002/hlca.19960790119
Publikováno v:
Helvetica Chimica Acta. 79:179-191
Synthesis of ‘Push-Pull’ Enynes ‘Push-pull’ enynes 1a–1f are easily available by Pd catalyzed coupling of stannyl-ynamines 15 and silylynamines 16 with β-iodo-enones 8 (Schemes 7 and 8).
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ede3e11c42241ece2a9273a374513dfb
https://doi.org/10.1002/hlca.19960790118
https://doi.org/10.1002/hlca.19960790118
Publikováno v:
ChemInform. 27
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dd9e3d786207def02266b13ebcfaac57
https://doi.org/10.1002/chin.199618078
https://doi.org/10.1002/chin.199618078
Publikováno v:
ChemInform. 27
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::45945c0dfaa480efc6f5c918a2ed6372
https://doi.org/10.1002/chin.199618077
https://doi.org/10.1002/chin.199618077
Publikováno v:
ChemInform. 30
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b47f2da5d83149008e52754a2d316e56
https://doi.org/10.1002/chin.199904135
https://doi.org/10.1002/chin.199904135
Publikováno v:
ChemInform. 30
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c048d94bfaafe7c2deacd95a4b1687ad
https://doi.org/10.1002/chin.199943068
https://doi.org/10.1002/chin.199943068