Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Sakellarios Trakossas"'
Autor:
Theodoros Panagiotidis, Efthymia G. Gioti, Evanthia P. Tolika, Anastasia-Aikaterini Varvogli, Stefanos S. Kotoulas, Thanos Andreou, John K. Gallos, Efstratios Neokosmidis, Theocharis V. Koftis, Theodoros Tsatsas, Sakellarios Trakossas, Elli Vastardi, Constantinos K. Zacharis, Elizabeth E. Anagnostaki
Publikováno v:
Tetrahedron. 74:519-527
A new synthesis of entecavir from d -glucose in an average total yield of 3.5% was achieved via an intramolecular nitrile oxide cycloaddition (INOC) reaction and a Peterson olefination as key-steps. The present process was designed for industrial app
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::010cdbad7486038f6a6b777f3e2bd3ef
https://doi.org/10.1016/j.tet.2017.12.034
https://doi.org/10.1016/j.tet.2017.12.034
Publikováno v:
Tetrahedron Letters. 52:1673-1676
Copper-catalyzed 1,3-dipolar cycloaddition of propargyl and azidoethyl thymine and adenine derivatives afforded triazole nucleosides bearing one or two base moieties. A catalytic role of the adenine nucleus was observed and is explained through coppe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::99b5cab9e6b563ea8f5cdf4d17f92e76
https://doi.org/10.1016/j.tetlet.2011.01.145
https://doi.org/10.1016/j.tetlet.2011.01.145
Publikováno v:
Tetrahedron. 67:1915-1923
Pyrrolidine analogues of C-nucleosides related to pseudouridine have been synthesized by 1,3-dipolar cycloaddition reactions of uracil-5 and 2,4-dimethoxypyrimidine-5 nitrones with allyl alcohol and methyl acrylate, and subsequent reductive cleavage
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3664ce72763da46302e078dc4c942b21
https://doi.org/10.1016/j.tet.2011.01.020
https://doi.org/10.1016/j.tet.2011.01.020
Autor:
Stella Manta, Dimitri Komiotis, Jan Balzarini, Evdoxia Coutouli-Argyropoulou, Ioannis Papasotiriou, Sakellarios Trakossas, Christos Kiritsis
A novel series of 3'-C-ethynyl and 3'-C-(1,4-disubstituted-1,2,3-triazolo) double-headed pyranonucleosides has been designed and synthesized. Reaction of 3-keto glucoside 1 with ethynyl magnesium bromide gave the desired precursor 3-C-ethynyl-1,2:5,6
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::259a144175f93ae0766871aff8779153
https://lirias.kuleuven.be/handle/123456789/352005
https://lirias.kuleuven.be/handle/123456789/352005
