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- An efficient, asymmetric organocatalyst-mediated conjugate addition of nitroalkanes to unsaturated cyclic and acyclic ketones. Claire E. T. Mitchell, Stacey E. Brenner, Jorge García-Fortanet, Steven V. Ley
, Org. Biomol. Chem.
, 2006
, 4
, 2039
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Ni(ii) and Pd(ii) pyridinyloxazolidine-compounds: synthesis, X-ray characterisation and catalytic activities in the aza-Michael reaction. G. Attilio Ardizzoia, Stefano Brenna, Bruno Therrien
, Dalton Trans.
, 2012
, 41
, 783
- Organocatalytic Michael addition–lactonisation of carboxylic acids using α,β-unsaturated trichloromethyl ketones as α,β-unsaturated ester equivalents. Louis C. Morrill, Daniel G. Stark, James E. Taylor, Siobhan R. Smith, James A. Squires, Agathe C. A. D'Hollander, Carmen Simal, Peter Shapland, Timothy J. C. O'Riordan, Andrew D. Smith
, Org. Biomol. Chem.
, 2014
, 12
, 9016
- Design, synthesis and biological evaluation of novel C3-functionalized oxindoles as potential Pim-1 kinase inhibitors. Hong-bao Sun, Xiao-yan Wang, Guo-bo Li, Li-dan Zhang, Jie Liu, Li-feng Zhao
, RSC Adv.
, 2015
, 5
, 29456
- The diastereoselectivity of electrophilic attack on trigonal carbon adjacent to a stereogenic centre: diastereoselective alkylation and protonation of open-chain enolates having a stereogenic centre at the β position. Ian Fleming, Jeremy J. Lewis
, J. Chem. Soc., Perkin Trans. 1
, 1992
, 3257
- Desulfitative Pd-catalysed coupling reaction using benzenesulfonyl chlorides and enones as the coupling partners. Kedong Yuan, Rui Sang, Jean-François Soulé, Henri Doucet
, Catal. Sci. Technol.
, 2015
, 5
, 2904
- Reactions of iodine(I) azide with αβ-unsaturated carbonyl compounds. Richard C. Cambie, Jeffrey L. Jurlina, Peter S. Rutledge, Bernard E. Swedlund, Paul D. Woodgate
, J. Chem. Soc., Perkin Trans. 1
, 1982
, 327
- The catalytic opportunities of near-critical water: a benign medium for conventionally acid and base catalyzed condensations for organic synthesis. Shane A. Nolen, Charles L. Liotta, Charles A. Eckert, Roger Gläser
, Green Chem.
, 2003
, 5
, 663
- Rhodium(iii)-catalyzed synthesis of trisubstituted furans via vinylic C–H bond activation. Mahadev Sharanappa Sherikar, Kiran R. Bettadapur, Veeranjaneyulu Lanke, Kandikere Ramaiah Prabhu
, Org. Biomol. Chem.
, 2021
, 19
, 7470
- Design, synthesis and biological evaluation of optically pure functionalized spiro[5,5]undecane-1,5,9-triones as HIV-1 inhibitors. Dhevalapally B. Ramachary, Y. Vijayendar Reddy, Atoshi Banerjee, Sharmistha Banerjee
, Org. Biomol. Chem.
, 2011
, 9
, 7282