Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Mohammed Dasser"'
Autor:
Annie Michaud, Mélanie Bolduc, Jérôme Bergeron, Nicholas Pelchat, Robert Chênevert, Pierre Morin, Mohammed Dasser
Publikováno v:
Tetrahedron: Asymmetry. 23:428-433
2-Substituted glycerol derivatives 4a–g were resolved by acylation with vinyl butyrate in the presence of lipases in organic media. The reverse reaction, the enzymatic hydrolysis of the corresponding butyrates 5a–g , was also highly stereoselecti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::691dcb1d4376e21e2ca82865b882f71c
https://doi.org/10.1016/j.tetasy.2012.04.001
https://doi.org/10.1016/j.tetasy.2012.04.001
Publikováno v:
Tetrahedron: Asymmetry. 19:1333-1338
The enzymatic desymmetrization of various meso-N-Boc-2,5-cis-disubstituted pyrrolidines and pyrrolines compounds by ester hydrolysis or transesterification provided the corresponding monoesters in high enantiomeric excess.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9afc0f726822434c7c1e2465fc0649fa
https://doi.org/10.1016/j.tetasy.2008.05.022
https://doi.org/10.1016/j.tetasy.2008.05.022
Publikováno v:
Tetrahedron: Asymmetry. 15:1889-1892
Phosphonotrixin is a herbicidal antibiotic characterized by a unique structure bearing a C–P bond on an isoprene unit. The formal enantioselective synthesis of ( S )-(−)-phosphonotrixin (ee = 93%) in nine steps and 12% overall yield from 1,3-dihy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::525df81ab384383f10ba6aca2cc790fd
https://doi.org/10.1016/j.tetasy.2004.04.046
https://doi.org/10.1016/j.tetasy.2004.04.046
Autor:
Pourashraf Mehrnaz, Russell C. Mauger, Steve Wesolowski, Phillip D Edwards, Simon Sydserff, Carine Lévesque, Maxime Tremblay, Thierry Groblewski, Vijayaratnam Santhakumar, Lois Ann Lazor, Bernstein Peter Robert, James Folmer, Pascall Giguère, William Potts, Denis Labrecque, Scott Throner, Joseph Cacciola, Mark Sylvester, Mohammed Dasser, Clay W Scott, Dean G. Brown, Andrew Griffin
Publikováno v:
Journal of medicinal chemistry. 57(3)
A new series of potent and selective histamine-3 receptor (H3R) antagonists was identified on the basis of an azaspiro[2.5]octane carboxamide scaffold. Many scaffold modifications were largely tolerated, resulting in nanomolar-potent compounds in the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::69954ef50a32d3a1cdac6f8403f68ac6
https://pubmed.ncbi.nlm.nih.gov/24410637
https://pubmed.ncbi.nlm.nih.gov/24410637
Autor:
Mohammed Dasser, Robert Chênevert
Publikováno v:
Canadian Journal of Chemistry. 78:275-279
Syringolide 2, a bacterial signal molecule which elicits active defence in resistant plants, has been synthesized in 9 steps from 2,3:4,5-di-O-isopropylidene-D-arabinose, a known derivative of D-arabinose.Key words: syringolide, arabinose, synthesis.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::385cd773d13fe00cc417216f4b2519b4
https://doi.org/10.1139/v99-252
https://doi.org/10.1139/v99-252
Publikováno v:
Tetrahedron: Asymmetry. 10:3117-3122
The stereoselective acylation of meso piperidines 3a , b by vinyl acetate (solvent and acyl donor) in the presence of Candida antarctica lipase gave the corresponding (2 S ,6 R ) and (2 S ,4 R ,6 R ) monoesters 2a , b in high enantiomeric purity. (5
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::25be376fc808a6087ccde0cb98c16294
https://doi.org/10.1016/s0957-4166(99)00315-8
https://doi.org/10.1016/s0957-4166(99)00315-8
Publikováno v:
Canadian Journal of Chemistry. 75:68-73
The C-3—C-9 main fragment of aspicilin was prepared via a fructose 1,6-diphosphate aldolase reaction. The same fragment was also synthesized by chemical transformation starting from D-arabinose. Key words: aldolase, aspicilin, arabinose, synthesis.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fa63943a7e2c25a709967713592c896b
https://doi.org/10.1139/v97-010
https://doi.org/10.1139/v97-010
Publikováno v:
ChemInform. 28
The C-3—C-9 main fragment of aspicilin was prepared via a fructose 1,6-diphosphate aldolase reaction. The same fragment was also synthesized by chemical transformation starting from D-arabinose. Key words: aldolase, aspicilin, arabinose, synthesis.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1a972ed339b57f697a34e9774d952aaa
https://doi.org/10.1002/chin.199732181
https://doi.org/10.1002/chin.199732181
Publikováno v:
ChemInform. 30
Enterolactone, a lignan isolated from biological fluids of animals and humans, was synthesized via enzymatic desymmetrization of 2-(3-methoxybenzyl)-1,3-propanediol.Key words: enterolactone, synthe...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b286935532097241aab2f46a33628212
https://doi.org/10.1002/chin.199934262
https://doi.org/10.1002/chin.199934262
Publikováno v:
ChemInform. 31
The stereoselective acylation of meso piperidines 3a , b by vinyl acetate (solvent and acyl donor) in the presence of Candida antarctica lipase gave the corresponding (2 S ,6 R ) and (2 S ,4 R ,6 R ) monoesters 2a , b in high enantiomeric purity. (5
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d4840a6c7e407a379a26e992018afba4
https://doi.org/10.1002/chin.200003220
https://doi.org/10.1002/chin.200003220