Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Nicholas Pelchat"'
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
Autor:
Michel Fila, Pierre Morin, Carine Lévesque, Annie Michaud, Nicholas Pelchat, Robert Chênevert
Publikováno v:
Tetrahedron: Asymmetry. 22:819-822
The enantioselective acylation (desymmetrization) of meso -7-azabicyclo[2.2.1]heptanediol 2 by vinyl acetate in the presence of Candida antarctica lipase B gave the corresponding (1 R ,2 R ,3 S ,4 S )-monoester 4 in high enantiomeric purity (ee ⩾ 9
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::803fec430f45c797efc4c26152b8cf22
https://doi.org/10.1016/j.tetasy.2011.05.016
https://doi.org/10.1016/j.tetasy.2011.05.016
Publikováno v:
Tetrahedron: Asymmetry. 20:1191-1196
Enzymatic acylation is commonly used for the kinetic resolution of alcohols and amines. The simple acyl group introduced during the enzymatic reaction is usually removed or replaced by another group. Retention of more complex acyl moieties as part of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::98e5c2204fb10e961e27ca3804f9381f
https://doi.org/10.1016/j.tetasy.2009.03.027
https://doi.org/10.1016/j.tetasy.2009.03.027
Publikováno v:
ChemInform. 40
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2269855186e9f55279074bd03c1da45a
https://doi.org/10.1002/chin.200931263
https://doi.org/10.1002/chin.200931263
Publikováno v:
Asymmetric Organic Synthesis with Enzymes
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4beb639ab2978b9d1fb6c8f7a876e176
https://doi.org/10.1002/9783527622481.ch6
https://doi.org/10.1002/9783527622481.ch6
Publikováno v:
The Journal of organic chemistry. 72(22)
Dolabriferol is a marine polypropionate characterized by an unusual noncontiguous carbon backbone. The two polypropionate subunits are linked by an ester function. The protected alcohol moiety of dolabriferol was synthesized via the enzymatic desymme
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::55081916dfdf6fcfdc3f303348cbb140
https://pubmed.ncbi.nlm.nih.gov/17910505
https://pubmed.ncbi.nlm.nih.gov/17910505
Publikováno v:
ChemInform. 38
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8071b06a3e5245b7d08719eef9b610de
https://doi.org/10.1002/chin.200707264
https://doi.org/10.1002/chin.200707264
Publikováno v:
Bioorganicmedicinal chemistry. 14(15)
The stereoselective acylation of the achiral chromanedimethanol derivative 1 by vinyl acetate in the presence of Candida antarctica lipase B gave the ( S )-monoester 2 in high enantiomeric purity (ee ⩾ 98%). Enzymatic hydrolysis of diesters of comp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::615f8b712f7af69269a33e27bb85bdad
https://pubmed.ncbi.nlm.nih.gov/16616508
https://pubmed.ncbi.nlm.nih.gov/16616508