Zobrazeno 1 - 10
of 36
pro vyhledávání: '"E. F. Llama"'
Publikováno v:
Enzyme and Microbial Technology. 30:895-901
The synthesis of ( R ) or ( S ) 1-chloro-3-(1-naphthyloxy)propan-2-ol, (2-Propranolol precursor) using yeast-catalysed reduction of 1-chloro-3-(1-naphthyloxy)propan-2-one, 1 is described. Several yeast strains have been used. The best strains were se
Publikováno v:
Biocatalysis and Biotransformation. 19:163-180
The importance of the adrenergic β-blockers with structure of (S) 1-aryloxy-3-amino-2-propanol in the treatment of different diseases has led the development of a variety of stereoselective synthetic methodologies for this stereoisomer. In this revi
Publikováno v:
Tetrahedron: Asymmetry. 11:4651-4660
The preparation of halohydrin β-blocker precursors using yeast-catalysed reduction of α-haloketones was performed. The influence in the yield and e.e. of several process variables was analysed. The (S)-enantioselectivity observed with Saccharomyces
Publikováno v:
Tetrahedron: Asymmetry. 10:3507-3514
The stereochemistry of the Candida antarctica lipase B (CALB) catalyzed resolution of diacetate 1 or diol 4 was analyzed. The primary and secondary acetate hydrolyses were studied separately using monoacetates 2 and 3 . The enantioselectivity of CALB
Publikováno v:
Tetrahedron Letters. 38:4137-4140
Amino-2-propanol structures can be obtained by addition to dibenzyl acetals of in situ generated dihalocarbenes using LVT (Low Valent Titanium). This methodology can be used to obtain adrenergic β-blockers with amino-2-propanol structure. Tetrahalom
Autor:
E. F. Llama, Ana Gradillas, C. Del Campo, J.M. Sánchez-Montero, M. Garcia, Jose‐Vicente Sinisterra
Publikováno v:
Biotechnology Letters. 19:999-1004
sThe hydrolysis of several esters catalyzed by lipase of Candida rugosa was used to analyse the interaction between the ester substrate and the active site and the geometry and steric restrictions of ‘alk‘, ‘ar‘ and ‘h‘ subsites. Using 4-
Publikováno v:
Tetrahedron: Asymmetry. 7:2485-2488
CAL offers increased ee, together with broad substrate structural tolerance that makes it a firm candidate for the resolution of BBAs of type 1 .
Publikováno v:
Tetrahedron: Asymmetry. 7:2627-2631
Synthesis of enantiomerically pure ( S )-(−)-propranolol, the most active of the widely used beta-blockers adrenergics, was achieved using a new chiral stationary phase (CSP) for the separation of a derivative. This simple methodology shows a signi
Publikováno v:
Journal of Molecular Catalysis A: Chemical. 95:179-192
The alteration of the selectivity of enzymes due to the immobilization methodology is discussed. The hydrolysis of esters of ( R,S ) 2-phenyl propionic and 2-phenyl butyric acids has been used as a reaction test. Lipases from Candida cylindracea immo
Autor:
José María Borrás Moreno, María José Cabezas, Carmen del Campo, José V. Sinisterra, E. F. Llama, Miguel Arroyo
Publikováno v:
J. Chem. Soc., Perkin Trans. 2. :1333-1336
The chemical modification of α-chymotrypsin by monomethoxypolyethylene glycol and the immobilization of lipases from Candida rugosa and C. antarctica on several supports changes the enantioselectivity of the enzymatic derivatives compared with the b