Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Hua Ming He"'
Autor:
Michael K. Manthey, Wayne Gerrard Reilly, Minoo J. Moghaddam, Vera J. Bender, Craig L. Francis, Xanthe E Wells, Hua Ming He-Williams, Robert George Whittaker
Publikováno v:
Drug Development Research. 46:302-308
The technology described in this article utilises the common laboratory reagent tris to readily produce drug–fatty acid conjugates. Tris has structural similarities to glycerol, allowing the coupling of one to three fatty acyl groups giving compoun
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::40b1d2e5473ee8e9c75dc703eaad8dfb
https://doi.org/10.1002/(sici)1098-2299(199903/04)46:3/4<302::aid-ddr16>3.0.co
https://doi.org/10.1002/(sici)1098-2299(199903/04)46:3/4<302::aid-ddr16>3.0.co
Autor:
Ahmad Nasiri, Paula Vihanto, Radka K. MIlanova, Jens J. Led, David Tanner, Tadashi Tsuda, Hiroyuki Nakata, Hua Ming He, Vladimir L. Florentiev, Harri Lönnberg
Publikováno v:
Acta Chemica Scandinavica. 47:592-596
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::00c7bf653c72dfd0059136ac35006faa
https://doi.org/10.3891/acta.chem.scand.47-0592
https://doi.org/10.3891/acta.chem.scand.47-0592
Publikováno v:
ChemInform. 22
A novel and diastereoselective entry to the β-lactam nucleus of the carbapenems starting from L-glutamic acid is exemplified by the synthesis of the potential (+)-PS-5 intermediate 13 .
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dd7315bb3e4fe74525b15cf5950843da
https://doi.org/10.1002/chin.199149291
https://doi.org/10.1002/chin.199149291
Publikováno v:
ChemInform. 23
Nucleophilic ring-opening of trans and cis aziridino alcohols 1 ( 1′ ) and 2 ( 2′ ) by hydride- and by methyl-transfer reagents has been studied. In general, good to excellent C-2 selectivity was observed (the regioselectivity being better for th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::784abd54ec252345aa4f8d1601858376
https://doi.org/10.1002/chin.199245092
https://doi.org/10.1002/chin.199245092
Autor:
David Tanner, Hua Ming He
Publikováno v:
Tetrahedron. 48:6079-6086
This paper describes two enantioselective aziridine-based routes toward 1β-methylthienamycin, 2, and related carbapenems, the key steps being completely regioselective ring-opening reactions of the chiral aziridines 7 and 10 with AlMe3.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2432b4f178f3559c334e33f8aa49e588
https://doi.org/10.1016/s0040-4020(01)89856-2
https://doi.org/10.1016/s0040-4020(01)89856-2
Publikováno v:
Tetrahedron. 48:6069-6078
Nucleophilic ring-opening of trans and cis aziridino alcohols 1 ( 1′ ) and 2 ( 2′ ) by hydride- and by methyl-transfer reagents has been studied. In general, good to excellent C-2 selectivity was observed (the regioselectivity being better for th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a452bbef2f742a0a1d3d8e850f0ff49e
https://doi.org/10.1016/s0040-4020(01)89855-0
https://doi.org/10.1016/s0040-4020(01)89855-0
Publikováno v:
Tetrahedron Letters. 32:283-286
A novel and diastereoselective entry to the β-lactam nucleus of the carbapenems starting from L-glutamic acid is exemplified by the synthesis of the potential (+)-PS-5 intermediate 13 .
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3a0d6088cbb749360adee8e0f88fed9a
https://doi.org/10.1016/0040-4039(91)80876-8
https://doi.org/10.1016/0040-4039(91)80876-8
Autor:
David Tanner, Hua Ming He
Publikováno v:
Tetrahedron. 45:4309-4316
A short enantioselective synthesis of the spirocyclic alkaloid (+)-Nitramine ( 1 ) is reported, the azaspiro ring system being formed via intramolecular ring-opening of the chiral epoxy sulfone 7 .
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::56894bde4f73149615b15b0f50d4e1a7
https://doi.org/10.1016/s0040-4020(01)81324-7
https://doi.org/10.1016/s0040-4020(01)81324-7
Autor:
Hua Ming He, David Tanner
Publikováno v:
ChemInform. 20
A short enantioselective synthesis of the spirocyclic alkaloid (+)-Nitramine ( 1 ) is reported, the azaspiro ring system being formed via intramolecular ring-opening of the chiral epoxy sulfone 7 .
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::aec2c009e020415b5be7eb3b698c5903
https://doi.org/10.1002/chin.198945318
https://doi.org/10.1002/chin.198945318