Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Maude Brossat"'
Autor:
Anne-Claude Dublanchet, Maude Brossat, Michel Philippe, Maria Dalko-Csiba, Julien Hitce, Jinzhu Xu, Marie-Céline Frantz
Publikováno v:
Current Opinion in Green and Sustainable Chemistry. 13:164-169
Sustainable innovation is a key-objective for our Group that has recently integrated the principles of sustainable development into all stages of a product's life cycle, from its design to consumer use. The following ambitious commitment: 100% of its
Autor:
Diego Hidalgo, Javier Palazon, Rosa M. Cusidó, Purificación Corchete, Lucie Tournier-Couturier, Maude Brossat, Virginie Steinmetz
Publikováno v:
Engineering in Life Sciences. 17:413-419
Centella asiatica is a herbaceous plant of Asian traditional medicine. Besides wound healing, this plant is recommended for the treatment or care of various skin conditions such as dry skin, leprosy, varicose ulcers, eczema, and/or psoriasis. Triterp
Autor:
Diego, Hidalgo, Virginie, Steinmetz, Maude, Brossat, Lucie, Tournier-Couturier, Rosa M, Cusido, Purificacion, Corchete, Javier, Palazon
Publikováno v:
Eng Life Sci
Centella asiatica is a herbaceous plant of Asian traditional medicine. Besides wound healing, this plant is recommended for the treatment or care of various skin conditions such as dry skin, leprosy, varicose ulcers, eczema, and/or psoriasis. Triterp
Autor:
Thomas S. Moody, Anita R. Maguire, Kevin S. Eccles, Alan Ford, Sarah L. Clarke, Nuala M. Maguire, Maude Brossat, Simon E. Lawrence
Publikováno v:
Tetrahedron: Asymmetry. 22:2144-2150
The preparation of enantiopure cyanohydrin acetates via enzymatic hydrolysis has been investigated by screening a range of biocatalysts and reaction conditions. Enzymatic resolution has been optimised through variation of the hydrolase biocatalyst an
Autor:
Maria Dalko-Csiba, Michel Philippe, Jinzhu Xu, Maude Brossat, Anne-Claude Dublanchet, Julien Hitce, Marie-Céline Frantz
Publikováno v:
Current Opinion in Green and Sustainable Chemistry. 13:171
Autor:
Simon E. Lawrence, Sinéad E. Milner, Anita R. Maguire, Curtis J. Elcoate, Maude Brossat, Thomas S. Moody
Publikováno v:
Tetrahedron: Asymmetry. 21:1011-1016
The kinetic bioresolution of 2-nitrocyclohexanol 1 was investigated by screening a range of hydrolases both for enantioselective transesterification and for enantioselective hydrolysis of the corresponding acetate. By appropriate choice of biocatalys
Publikováno v:
Tetrahedron: Asymmetry. 20:2112-2116
An efficient hydrolase-catalyzed bioresolution of tertiary amino ester protic ionic liquids has been demonstrated. Protic ionic liquids have been prepared in one step from the corresponding tertiary amino alcohols by treatment with butyric anhydride.
Publikováno v:
Organic Process Research & Development. 13:706-709
A separation tool involving the use of a vinyl ester amino acid as acyl donor in a bioresolution has been developed. The acid-washable acyl group acts as a removable tag, facilitating separation of the secondary alcohol from the bioresolution product
Hydrolase catalysed kinetic resolutions leading to a series of 3-aryl alkanoic acids (⩾94% ee) are described. Hydrolysis of the ethyl esters with a series of hydrolases was undertaken to identify biocatalysts that yield the corresponding acids with
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e35fde12de6e0f280257a05675cf9faf
https://hdl.handle.net/10468/575
https://hdl.handle.net/10468/575
Publikováno v:
Tetrahedron
Tetrahedron, Elsevier, 2006, 62 (13), pp.3052-3055. ⟨10.1016/j.tet.2006.01.031⟩
Tetrahedron, 2006, 62 (13), pp.3052-3055. ⟨10.1016/j.tet.2006.01.031⟩
Tetrahedron, Elsevier, 2006, 62 (13), pp.3052-3055. ⟨10.1016/j.tet.2006.01.031⟩
Tetrahedron, 2006, 62 (13), pp.3052-3055. ⟨10.1016/j.tet.2006.01.031⟩
The 11β-hydroxymethyl-androst-4-en-3,17-dione 5 was prepared within five synthetic steps starting from the commercially available adrenosterone with an overall yield of 24%. The 11-ketosteroid 1 was subjected to a Peterson methylenation. The subsequ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b8e016b4b8a5111e58a361181f5304d5
https://hal.archives-ouvertes.fr/hal-01443313
https://hal.archives-ouvertes.fr/hal-01443313