Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Miroslav Terinek"'
Publikováno v:
The Journal of organic chemistry. 80(23)
An asymmetric total synthesis of the nootropic alkaloid (-)-huperzine A was completed using a cascade sequence initiated by an intramolecular aza-Prins reaction and terminated by a stereoelectronically guided fragmentation of a cyclobutylcarbinyl cat
Autor:
Miroslav Terinek, Andrea Vasella
Publikováno v:
Helvetica Chimica Acta. 88:10-22
The gluco-configured analogue 15 of nagstatin (1) and the methyl ester 14 were synthesized via condensation of the thionolactams 17 or 18 with the β-amino ester 19. The silyl ethers 20 and 21 resulting from 17 were desilylated to 22 and 23; these al
Autor:
Miroslav Terinek, Andrea Vasella
Publikováno v:
Tetrahedron: Asymmetry. 16:449-469
The inhibition of snail β-mannosidase by the manno-configured amino- and hydroxy-lactams and -imidazoles 7–10 was compared to the inhibition of the β-glucosidases from Caldocellum saccharolyticum and from sweet almonds by the gluco-configured ami
Autor:
Andrea Vasella, Miroslav Terinek
Publikováno v:
Helvetica Chimica Acta. 87:3035-3049
The gluco- and manno-tetrahydropyridoimidazole-2-acetates and -acetic acids 16 and 17, and 20 and 21, respectively, were synthesized by condensation, in the presence of HgCl2, of the known thionolactam 26 with the β-amino ester 25 that was obtained
Autor:
Andrea Vasella, Miroslav Terinek
Publikováno v:
Helvetica Chimica Acta. 86:3482-3509
It was shown that retaining β-glucosidases and galactosidases of families 1–3 feature a strong interaction between C(2)OH of the substrate and the catalytic nucleophile. An analogous interaction can hardly take place for retaining β-mannosidases.
Publikováno v:
Collection of Czechoslovak Chemical Communications. 62:1325-1341
Four optically pure isomers of methyl 11,16-dihydroxy-16-methyl-9-oxoprost-13-enoate (1a-1d) were synthesized using an approach reverse to the classical Corey procedure, the key intermediates being the easily accessible (-)- and (+)-enantiomers of th
Publikováno v:
Organic letters. 15(4)
The acetylcholinesterase inhibitor (-)-huperzine A was synthesized from (S)-4-hydroxycyclohex-2-enone in 17 steps by a route that involved two cyclobutane fragmentations. The first of these employed a retro-aldol cleavage to generate the α-pyridone
Publikováno v:
ChemInform. 28
Four optically pure isomers of methyl 11,16-dihydroxy-16-methyl-9-oxoprost-13-enoate (1a-1d) were synthesized using an approach reverse to the classical Corey procedure, the key intermediates being the easily accessible (-)- and (+)-enantiomers of th
Autor:
Andrea Vasella, Miroslav Terinek
Publikováno v:
ChemInform. 35
The D-manno-tetrahydroimidazopyridine-2-phosphonate 11 was prepared via a high-yielding Pd(PPh3)(4)-catalysed diphenylphosphonylation of the manno-iodoimidazole 12, followed by transesterification to the diethyl phosphonate 14 and dealkylation, provi
Autor:
Andrea Vasella, Miroslav Terinek
Publikováno v:
XXIst International Carbohydrate Symposium 2002.