Zobrazeno 1 - 10
of 19
pro vyhledávání: '"K.-H. Budt"'
Publikováno v:
ChemInform. 24
The synthesis of the previously not accessible symmetrical bis(α-aminoalkyl)phosphinic acids is demonstrated. These compounds are valuable central building blocks in the synthesis of HIV protease inhibitors.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f2672f81e19b04bf10c9e617b1394d04
https://doi.org/10.1002/chin.199301254
https://doi.org/10.1002/chin.199301254
Publikováno v:
ChemInform. 24
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e60eee7f169f2c3c16889fcd66e0fd77
https://doi.org/10.1002/chin.199303282
https://doi.org/10.1002/chin.199303282
Publikováno v:
ChemInform. 24
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::49b51850caf166741516e5797d039011
https://doi.org/10.1002/chin.199312237
https://doi.org/10.1002/chin.199312237
Publikováno v:
ChemInform. 25
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::64b6f0b22f3aea200b29175e516b66cf
https://doi.org/10.1002/chin.199414220
https://doi.org/10.1002/chin.199414220
Publikováno v:
Tetrahedron Letters. 33:5331-5334
Alkylphosphonous acid diesters MeP(OR)2 3a-b were shown to be highly effctive and mild reducing reagents in the oxalimide cyclization of azetidinone-1-oxalyl-4-di- or tri-thiocarbonates or 4-thioesters 1a-t forming penems 2a-t at lower temperature sh
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2183df516ac109cf4b5ab4c1f186bec6
https://doi.org/10.1016/s0040-4039(00)79085-x
https://doi.org/10.1016/s0040-4039(00)79085-x
Publikováno v:
Tetrahedron Letters. 33:4549-4552
The synthesis of the previously not accessible symmetrical bis(α-aminoalkyl)phosphinic acids is demonstrated. These compounds are valuable central building blocks in the synthesis of HIV protease inhibitors.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::11df054519bc10fd52cf499102bc2fe9
https://doi.org/10.1016/s0040-4039(00)61309-6
https://doi.org/10.1016/s0040-4039(00)61309-6
Autor:
Anusch Peyman, Jutta Dr Hansen, K.‐H. Budt, Jörg Spanig, Irvin Winkler, D. Ruppert, J. Knolle, C. Meichsner, Arnold Dr. Paessens, Bernd Stowasser, L. Jian-Qi
Publisher Summary This chapter describes a series of inhibitors in which a central building block, containing a transition-state mimetic and the P1 and P1’ residues of the HIV-PR cleavage site, is placed in a C 2 -symmetrical peptidic environment a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d6c2b2a60e7d427e044faac8f52112c2
https://doi.org/10.1016/s0165-7208(97)80081-5
https://doi.org/10.1016/s0165-7208(97)80081-5
Autor:
L. Pavlitzkova, J. Kay, K.-H. Budt, T. Schulze, L. H. Pearl, M. Nawrath, K. Moelling, M. Souček, M.-T. Knoop, V. Kruft
Publikováno v:
Retroviral Proteases ISBN: 9780333536124
The pol-gene of HIV-1 expressed in bacteria undergoes autocatalytic processing which results in the generation of the p66 reverse transcriptase (RT)/RN ase H, the p32 endonuclease and the p9 protease. The partially purified protease generates in vitr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8ed7d8b237ca3dc399dfec4a5d5e7192
https://doi.org/10.1007/978-1-349-11907-3_4
https://doi.org/10.1007/978-1-349-11907-3_4
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