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Molecular Diversity|January 24, 2015
One-step synthesis of azole- and benzazole-based sulfonamides in aqueous mediaHassan Zali-Boeini, Zhaleh Najafi, Bahareh Abtahi, et al.
Molecular Diversity|September 22, 2012
Molecular docking and receptor-specific 3D-QSAR studies of acetylcholinesterase inhibitorsPran Kishore Deb, Anuradha Sharma, Poonam Piplani, et al.
Molecular Diversity|September 20, 2012
Catalyst-free synthesis of quinazolin-4-ones from (hetero)aryl-guanidines: application to the synthesis of pyrazolo[4,3-f]quinazolin-9-ones, a new family of DYRK1A inhibitorsJulien Debray, Simon Bonte, Olivier Lozach, et al.
Molecular Diversity|July 4, 2012
Exploring a sulfone linker utilizing trimethyl aluminum as a cleavage reagent: solid-phase synthesis of sulfonamides and ureasTsai-Wen Chung, Chih-Hau Chen, Chu-Chung Lin, et al.
Molecular Diversity|July 4, 2012
Focused enumeration and assessing the structural diversity of scaffold libraries: conformationally restricted bicyclic secondary diaminesOleksandr O Grygorenko, Roman Prytulyak, Dmitriy M Volochnyuk, et al.
Molecular Diversity|March 26, 2010
A novel regiospecific cascade synthesis of sulfonamide derivatives from N-(2-polychloroethyl)sulfonamides via chloroaziridine intermediates in the presence of mercaptoethanolIgor B Rozentsveig, Aleksandr V Popov, Gulnur N Rozentsveig, et al.
Molecular Diversity|March 23, 2010
Predictive models for nucleoside bisubstrate analogs as inhibitors of siderophore biosynthesis in Mycobacterium tuberculosis: pharmacophore mapping and chemometric QSAR studyNilesh R Tawari, Mariam S Degani
Molecular Diversity|January 1, 1997
Solid phase synthesis of allylic alcohols via the Baylis-Hillman reactionH Richter, G Jung
Molecular Diversity|October 14, 2018
One-pot solvent-free synthesis of 2,3-dihydro-2-substituted-1H-naphtho[1,2-e][1,3]oxazine derivatives using Fe3O4@nano-cellulose/TiCl as a bio-based and recyclable magnetic nano-catalystSara Azad, Bi Bi Fatemeh Mirjalili
Molecular Diversity|October 5, 2018
Design, synthesis and in vitro evaluation of a Dopa-organoboron compound that acts as a bladder relaxant through non-catecholamine receptorsAna L Ocampo-Néstor, Ruth M López-Mayorga, Enrique F Castillo-Henkel, et al.
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