Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Nicola Catozzi"'
Publikováno v:
Tetrahedron Letters. 49:2865-2868
A new, short and efficient route to louisianins C and D is described in which the pyridine ring is constructed from a disubstituted 1,2,4-triazine by an inverse-electron-demand Diels–Alder/retro-Diels–Alder/aromatisation cascade sequence. This ei
Publikováno v:
Synlett. 2007:2217-2221
A new and straightforward procedure is described for the preparation of highly substituted pyridines and pyridazines. The method involves a Diels-Alder/retro-Diels-Alder sequence leading to dihydropyridine or related intermediates, which can be aroma
Publikováno v:
The Journal of Organic Chemistry. 70:9257-9268
[Reaction: see text]. A collection of 13 unsymmetrical ketones, each one featuring a sugar (d-glucosyl, d-galactosyl, d-mannosyl, and l-fucosyl) and an aglycone moiety (phenyl, 2-thiazolyl, TMS-ethynyl, allyl, and 1-propenyl) was prepared by a unifor
Publikováno v:
ChemInform. 41
Isolated in 1995, the four members of the louisianin family (A, B, C and D) are simple pyridine and 2-pyridone alkaloids that display both antibacterial and anticancer activity. Herein we describe the synthesis of all four members of the louisianin f
Publikováno v:
The Journal of organic chemistry. 74(21)
Isolated in 1995, the four members of the louisianin family (A, B, C and D) are simple pyridine and 2-pyridone alkaloids that display both antibacterial and anticancer activity. Herein we describe the synthesis of all four members of the louisianin f
Publikováno v:
ChemInform. 39
An efficient synthesis of O-benzylated derivatives of the title sugar aldehydes via thiazole addition to tri-O-benzyl-l-fuconolactone followed by highly stereoselective deoxygenation of the resulting thiazolylketose and thiazole to formyl transformat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::60991a550f2beb31eaadce1d11fd7144
http://hdl.handle.net/11392/1201393
http://hdl.handle.net/11392/1201393