Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Daniel Chapdelaine"'
Autor:
Nassim Benyerbah, Pompilia Ispas-Szabo, Khalil Sakeer, Daniel Chapdelaine, Mircea Alexandru Mateescu
Publikováno v:
Pharmaceutics, Vol 11, Iss 6, p 253 (2019)
The potential of the polyampholytic and polyelectrolytic starch compounds as excipients for drug controlled release was investigated using various tracers differing in terms of solubility and permeability. Ampholytic trimethylaminecarboxymethylstarch
Externí odkaz:
https://doaj.org/article/4c40531e329b42a4b62f7237db233f0c
Autor:
Daniel Chapdelaine, Pierre-Olivier Montiglio, Oscar Quintana Sanchez, Caroline Provost, Mathieu Lemieux, François Dumont, Laura Chouinard-Thuly
Publikováno v:
Journal of Applied Entomology. 144:331-334
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::af70aa7951ad4e32dabef8245211f63a
https://doi.org/10.1111/jen.12735
https://doi.org/10.1111/jen.12735
Autor:
Cindy Buonomano, Yvan Guindon, Daniel Chapdelaine, François Godin, Jacques Rodrigue, Karine Houde, Thao Trinh, Martin Duplessis, André Boutros
Publikováno v:
Org. Chem. Front.. 1:974-982
Reported herein is the synthesis of all possible stereotriad propionates derived from L-lactic acid and L-alanine. The approach is based on a stereocontrolled Mukaiyama aldol reaction followed by a free radical-mediated hydrogen transfer, for which t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4e6cefa7db40a524412d189f7901da73
https://doi.org/10.1039/c4qo00142g
https://doi.org/10.1039/c4qo00142g
Autor:
Daniel Chapdelaine, Taoufik Ben Halima
Publikováno v:
Synlett. 23:1675-1677
Phenones can be efficiently transformed into β-substituted chalcones in a two-step process. First, propargylic alcohols were obtained by addition of ethoxyacetylene anion to aromatic ketones. Activation of the propargylic alcohols using a catalytic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cd0c280c91bd5a3479d4b023f119e6a0
https://doi.org/10.1055/s-0031-1290677
https://doi.org/10.1055/s-0031-1290677
Publikováno v:
The Journal of Organic Chemistry. 67:5669-5672
Synthesis of the highly biologically valuable cardenolide backbone was achieved via anionic polycyclization. Bromoketone 18, obtained from double-Michael cycloaddition between cyclohexenone 14 and gamma,delta-unsaturated beta-ketoester 16, was effici
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::95b69a5f74e877fb7c938921552aed56
https://doi.org/10.1021/jo025612b
https://doi.org/10.1021/jo025612b
Autor:
Daniel Chapdelaine, Taoufik Ben Halima
Publikováno v:
ChemInform. 43
The products are of interest as biological agents and as intermediates for flavone structures.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::59c548baed69d922d6d2826eca2f3374
https://doi.org/10.1002/chin.201243079
https://doi.org/10.1002/chin.201243079
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:
Synlett. 1994:660-662
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2891f6f3f68aa13d1a7230cc99502a4d
https://doi.org/10.1055/s-1994-22966
https://doi.org/10.1055/s-1994-22966