Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Adrian Häberli"'
Publikováno v:
Journal of Pharmaceutical and Biomedical Analysis. 53:24-28
An interaction product of aminotadalafil was isolated from an illegal health food product. The structure of the interaction product was elucidated by means of IR, NMR, and mass spectroscopy. The hitherto unknown compound was characterized as condensa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4b2a98e96652d1e81aebc89dff362111
https://doi.org/10.1016/j.jpba.2010.03.008
https://doi.org/10.1016/j.jpba.2010.03.008
Publikováno v:
Helvetica Chimica Acta. 83:328-335
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::abec993c4e444659bb5c50001cb8ea7f
https://doi.org/10.1002/(sici)1522-2675(20000216)83:2<328::aid-hlca328>3.0.co
https://doi.org/10.1002/(sici)1522-2675(20000216)83:2<328::aid-hlca328>3.0.co
Autor:
Adrian Häberli, Hanspeter Pfander
Publikováno v:
Helvetica Chimica Acta. 82:696-706
The three apocarotenoids methyl (9Z)-8′-oxo-6,8′-diapocaroten-6-oate (2), methyl (9Z)-10′-oxo-6,10′-diapocaroten-6-oate (4), and methyl (9Z)-14′-oxo-6,14′-diapocaroten-6-oate (5), recently isolated from annatto, were synthesized. The key
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9026272a8213dda08b2cf9fbd9fe5671
https://doi.org/10.1002/(sici)1522-2675(19990505)82:5<696::aid-hlca696>3.0.co
https://doi.org/10.1002/(sici)1522-2675(19990505)82:5<696::aid-hlca696>3.0.co
Publikováno v:
Nucleosides, Nucleotides and Nucleic Acids. 22:1187-1189
We synthesized pyrrolidino-C-nucleosides, incorporated them into oligodeoxynucleotides and investigated their pairing properties. The thermal duplex and triplex stabilities were measured. While triplex formation is destabilized in the case of pyrroli
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::81f85072ea709e51e371a6fb489e6fbb
https://doi.org/10.1081/ncn-120022832
https://doi.org/10.1081/ncn-120022832
Publikováno v:
Angewandte Chemie. 113:3101-3103
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::48ac413b8ab62e2b037dc92b0b37981f
https://doi.org/10.1002/1521-3757(20010817)113:16<3101::aid-ange3101>3.0.co
https://doi.org/10.1002/1521-3757(20010817)113:16<3101::aid-ange3101>3.0.co
Publikováno v:
Angewandte Chemie International Edition. 40:3012-3014
The stabilizing effect of a dG:dC base-pair can also be imparted to a DNA duplex by a non-hydrogen-bonding, non-shape-complementary nucleoside analogue when interstrand stacking interactions come into play. This is the case, for example, with dBP, wh
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fb117dc1fe8fbca5b8da4100be692408
https://doi.org/10.1002/1521-3773(20010817)40:16<3012::aid-anie3012>3.0.co
https://doi.org/10.1002/1521-3773(20010817)40:16<3012::aid-anie3012>3.0.co
Autor:
Adrian Häberli, Christian J. Leumann
Publikováno v:
Organic letters. 3(3)
[figure: see text] A novel method for the synthesis of pyrrolidine C-nucleosides has been developed. The key step of the synthesis is the palladium(0)-mediated coupling of a disubstituted N-protected 2-pyrroline and 5-iodouracil. C-Nucleoside 14 and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::050ae0afa397a40fc2bb675a60757731
https://pubmed.ncbi.nlm.nih.gov/11428045
https://pubmed.ncbi.nlm.nih.gov/11428045
Publikováno v:
Journal of Natural Products. 64:1254-1255
From the fruits of Asparagus falcatus a novel minor (Z)-carotenoid has been isolated and, on the basis of spectral data interpretation, characterized as (9Z)-capsanthin-5,6-epoxide [(9Z,3S,5R,6S,3'S,5'R)-5,6-epoxy-3,3'-dihydroxy-5,6-dihydro-beta,kapp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fcd947025a0bc385df50e2ffd399592c
https://doi.org/10.1021/np0101447
https://doi.org/10.1021/np0101447
Publikováno v:
Organic & Biomolecular Chemistry. 3:1653
Pyrrolidino pseudo-C-nucleosides are isosteres of natural deoxynucleosides which are protonated at the pyrrolidino ring nitrogen under physiological conditions. As constituents of a triplex forming oligodeoxynucleotide (TFO), the positive charge is e
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dfa89b503405a58248602028c23d3814
https://doi.org/10.1039/b502799c
https://doi.org/10.1039/b502799c
Publikováno v:
Helvetica Chimica Acta. 85:1327
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::da32ef0018bae2a4405d15d88966ef4f
https://doi.org/10.1002/1522-2675(200205)85:5<1327::aid-hlca1327>3.0.co
https://doi.org/10.1002/1522-2675(200205)85:5<1327::aid-hlca1327>3.0.co