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327José M. Concellón, Humberto Rodríguez-Solla, Carmen Concellón and Vicente del Amo.
Stereospecific and highly stereoselective cyclopropanation reactions promoted by samarium, Chem. Soc. Rev., 2010, 39, 4103. Kovuru Gopalaiah and Henri B. Kagan.
Use of samarium diiodide in the field of asymmetric synthesis, New J. Chem., 2008, 32, 607. Christine Beemelmanns and Hans-Ulrich Reissig.
Highly diastereoselective samarium diiodide induced cyclizations of new 3-substituted indole derivatives, Org. Biomol. Chem., 2009, 7, 4475. Michal Szostak, Malcolm Spain and David J. Procter.
Electron transfer reduction of unactivated esters using SmI2–H2O, Chem. Commun., 2011, 47, 10254. Christine Beemelmanns and Hans-Ulrich Reissig.
Samarium diiodide induced ketyl-(het)arene cyclisations towards novel N-heterocycles, Chem. Soc. Rev., 2011, 40, 2199. Michal Szostak, Malcolm Spain, Dixit Parmar and David J. Procter.
Selective reductive transformations using samarium diiodide-water, Chem. Commun., 2012, 48, 330. Todd Maisano, Kevin E. Tempest, Dhandapani V. Sadasivam and Robert A. Flowers, II.
A convenient pathway to Sm(ii)-mediated chemistry in acetonitrile, Org. Biomol. Chem., 2011, 9, 1714. Toshio Honda, Tomoha Matsukawa and Kazunori Takahashi.
Efficient total synthesis of (−)-stemoamide, Org. Biomol. Chem., 2011, 9, 673. Raymond J. Boffey, William G. Whittingham and Jeremy D. Kilburn.
Diastereoselective SmI mediated cascade radical cyclisations of methylenecyclopropane derivatives—syntheses of paeonilactone B and 6-epi-paeonilactone A, J. Chem. Soc., Perkin Trans. 1, 2001, 0, 487. Stephen G. Davies, Humberto Rodríguez-Solla, Juan A. Tamayo, Andrew R. Cowley, Carmen Concellón, A. Christopher Garner, Alastair L. Parkes and Andrew D. Smith.
Asymmetric conjugate reductions with samarium diiodide: asymmetric synthesis of (2S,3R)- and (2S,3S)-[2-H,3-H]-leucine-(S)-phenylalanine dipeptides and (2S,3R)-[2-H,3-H]-phenylalanine methyl ester, Org. Biomol. Chem., 2005, 3, 1435.