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Current Opinion in Drug Discovery & Development|February 5, 2004
Rapid assembly of molecular diversity via exploitation of isocyanide-based multi-component reactionsChristopher Hulme, Thomas NixeyOrganic & Biomolecular Chemistry|August 6, 2013
Bifunctional building blocks in the Ugi-azide condensation reaction: a general strategy toward exploration of new molecular diversitySteven Gunawan, Christopher HulmeCurrent Medicinal Chemistry|February 7, 2003
"Multi-component reactions : emerging chemistry in drug discovery" 'from xylocain to crixivan'Christopher Hulme, Vijay GoreMolecular Diversity|February 12, 2009
Emerging molecular diversity from the intra-molecular Ugi reaction: iterative efficiency in medicinal chemistryChristopher Hulme, Justin DietrichTetrahedron Letters|September 3, 2013
Construction of functionalized tricyclic dihydropyrazino-quinazolinedione chemotypes via an Ugi/N-acyliminium ion cyclization cascadeSteven Gunawan, Christopher HulmeTetrahedron Letters|June 24, 2014
Exploiting the Divalent Nature of Isonitriles: a novel Pictet-Spengler Amidination processFederico Medda, Christopher HulmeMolecular Informatics|August 3, 2016
Rough Set Theory as an Interpretable Method for Predicting the Inhibition of Cytochrome P450 1A2 and 2D6Julien Burton, Joachim Petit, Emeric Danloy, et al.Organic Letters|February 24, 2012
Straightforward assembly of phenylimidazoquinoxalines via a one-pot two-step MCR processFabio De Moliner, Christopher HulmeMolecular Diversity|April 15, 2008
Emerging approaches for the syntheses of bicyclic imidazo[1,2-x]-heterocyclesChristopher Hulme, Yeon-Sun LeeTetrahedron Letters|March 19, 2013
A Van Leusen deprotection-cyclization strategy as a fast entry into two imidazoquinoxaline familiesFabio De Moliner, Christopher HulmePageof 11