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137Chen et al..
A biomolecule-compatible visible-light-induced azide reduction from a DNA-encoded reaction-discovery system, Nature Chemistry, 2011 Leibfarth et al..
A facile route to ketene-functionalized polymers for general materials applications, Nature Chemistry, 2010 Bo Jiang, Wen-Juan Hao, Jin-Peng Zhang, Shu-Jiang Tu and Feng Shi.
A new domino autocatalytic reaction leading to polyfunctionalized spiro[5.5]undecanes and dispiro[4.2.5.2]pentadecanes, Org. Biomol. Chem., 2009, 7, 2195. Hamish McNab, Mark Morrow, Simon Parsons, David A. Shannon and Kirsti Withell.
Synthetic routes to pyrrolizine-1,5-dione derivatives by flash vacuum pyrolysis of amidomethylene derivatives of Meldrum's acid, Org. Biomol. Chem., 2009, 7, 4936. Martin WolffsThese authors contributed equally to the work., Matthew J. Kade and Craig J. Hawker.
An energy efficient and facile synthesis of high molecular weight polyesters using ketenes, Chem. Commun., 2011, 47, 10572. Kyle L. Kimmel, Jimmie D. Weaver and Jonathan A. Ellman.
Enantio- and diastereoselective addition of cyclohexyl Meldrum's acid to β- and α,β-disubstituted nitroalkenes via N-sulfinyl urea catalysis, Chem. Sci., 2012, 3, 121. Michal Beit-Yannai, Xin Chen and Zvi Rappoport.
Amine catalysis in the vinylic substitution of a-methylthio-a-arylmethylene Meldrum's acids and its absence in the substitution of methyl ß-iodo-a-nitrocinnamate by amines, J. Chem. Soc., Perkin Trans. 2, 2001, 0, 1534. Abd El-Aal M. Gaber, Gordon A. Hunter and Hamish McNab.
3-Hydroxypyrroles and 1H-pyrrol-3(2H)-ones. Part 14. Pyrolysis of oxazolidinylmethylene derivatives of Meldrum's acid – synthesis of N-alkenyl-3-hydroxypyrroles and related reactions, J. Chem. Soc., Perkin Trans. 1, 2002, 0, 548. Atul Kumar, Promod Kumar, Vishwa Deepak Tripathi and Suman Srivastava.
A novel access to indole-3-substituted dihydrocoumarins in artificial sweetener saccharin based functional ionic liquids, RSC Advances, 2012, 2, 11641. Alexander J. Blake, David Clarke, Richard W. Mares and Hamish McNab.
Synthesis and chemistry of 3-tert-butyl-1,5-diaminopyrazole, Org. Biomol. Chem., 2003, 1, 4268.