Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Isabelle Thumin"'
Publikováno v:
ChemInform. 33
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::70a2a68ae9a763f6899c74af97e8f14e
https://doi.org/10.1002/chin.200223222
https://doi.org/10.1002/chin.200223222
Autor:
Michel Prévost, Marc Gagnon, Benoit Cardinal-David, Isabelle Thumin, Yvan Guindon, Daniel Chapdelaine
Publikováno v:
ChemInform. 41
D- and L-nucleosides and analogues thereof, including the 4'-thionucleoside series, are one of the most important biological and pharmaceutically active classes of compounds. A novel approach to their synthesis from chiral acyclic thioaminal, bearing
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::21faa90f009994c7051a92c8a9bf798f
https://doi.org/10.1002/chin.201015199
https://doi.org/10.1002/chin.201015199
Autor:
Yvan Guindon, Daniel Chapdelaine, Michel Prévost, Marc Gagnon, Isabelle Thumin, Benoit Cardinal-David
Publikováno v:
Journal of the American Chemical Society. 131(47)
D- and L-nucleosides and analogues thereof, including the 4'-thionucleoside series, are one of the most important biological and pharmaceutically active classes of compounds. A novel approach to their synthesis from chiral acyclic thioaminal, bearing
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::493051aa60712f2aa9cf25fbd9c90f35
https://pubmed.ncbi.nlm.nih.gov/19902939
https://pubmed.ncbi.nlm.nih.gov/19902939
Publikováno v:
Organic letters. 4(2)
[reaction: see text] Acyclic diastereoselection is achieved for the formation of thioaminyl acetals. The highly intramolecular stereocontrolled S(N)2 displacement of the thioaminyls allows for the formation of cyclic nucleoside derivatives. This vers
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::78e2c8ed5d76ae573450bdf536e38f8b
https://pubmed.ncbi.nlm.nih.gov/11796060
https://pubmed.ncbi.nlm.nih.gov/11796060