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Journal of the American Chemical Society|August 5, 2004
3-nitro-3-deaza-2'-deoxyadenosine as a versatile photocleavable 2'-deoxyadenosine mimicCaroline Crey-Desbiolles, Jean Lhomme, Pascal Dumy, et al.Bioorganic & Medicinal Chemistry Letters|May 6, 2004
The oxime bond formation as an efficient chemical tool for the preparation of 3',5'-bifunctionalised oligodeoxyribonucleotidesOm Prakash Edupuganti, Olivier Renaudet, Eric Defrancq, et al.Chemistry (Weinheim an Der Bergstrasse, Germany)|October 17, 2017
Everything You Always Wanted to Know about Poly-l-lysine Dendrigrafts (But Were Afraid to Ask)Jean-Patrick Francoia, Laurent VialChemical Communications (Cambridge, England)|October 20, 2015
A KISS (keep it simple, sensor) array for glycosaminoglycansJean-Patrick Francoia, Laurent VialBioorganic & Medicinal Chemistry Letters|April 2, 2008
Use of gamma-aminopropyl-coated glass surface for the patterning of oligonucleotides through oxime bond formationNabil Dendane, Antoine Hoang, Eric Defrancq, et al.Chemical Communications (Cambridge, England)|October 15, 2013
Expanding the scope of oxime ligation: facile synthesis of large cyclopeptide-based glycodendrimersBaptiste Thomas, Nathalie Berthet, Julian Garcia, et al.Chemistry (Weinheim an Der Bergstrasse, Germany)|December 5, 2013
Oxime ligation: a chemoselective click-type reaction for accessing multifunctional biomolecular constructsSébastien Ulrich, Didier Boturyn, Alberto Marra, et al.The Journal of Organic Chemistry|March 11, 2006
Chemoselectively addressable template: a valuable tool for the engineering of molecular conjugatesElisabeth Garanger, Didier Boturyn, Olivier Renaudet, et al.Bioorganic & Medicinal Chemistry Letters|January 31, 2006
Nitrobenzylcarbamate prodrugs of cytotoxic acridines for potential use with nitroreductase gene-directed enzyme prodrug therapyChristian Asche, Pascal Dumy, Danièle Carrez, et al.Bioorganic & Medicinal Chemistry Letters|June 30, 2009
Functionalization of the A ring of pyridoacridine as a route toward greater structural diversity. Synthesis of an octacyclic analogue of eilatinLaurent Bouffier, Rodica Dinica, Julien Debray, et al.Pageof 19