cheminform abstract: iron-catalyzed asymmetric olefin cis-dihydroxylation with 97% enantiomeric...

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2008 Hydroxylation O 0216 Iron-Catalyzed Asymmetric Olefin cis-Dihydroxylation with 97% Enantiomeric Excess. — Several bis(2-pyridylmethyl)-1,2-bipyrrolidine ligands are prepared by lit- erature processes and their iron(II) complexes investigated in the cis-dihydroxylation of olefins. For the first time, a synthetic nonheme iron catalyst shows enantioselectiv- ities comparable with those obtained with the osmium-based AD mixes. — (SUZUKI, K.; OLDENBURG, P. D.; QUE*, L. J.; Angew. Chem., Int. Ed. 47 (2008) 10, 1887-1889; Dep. Chem., Univ. Minn., Minneapolis, MN 55455, USA; Eng.) — Kieslich 27- 041

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Page 1: ChemInform Abstract: Iron-Catalyzed Asymmetric Olefin cis-Dihydroxylation with 97% Enantiomeric Excess

2008

HydroxylationO 0216 Iron-Catalyzed Asymmetric Olefin cis-Dihydroxylation with 97% Enantiomeric

Excess. — Several bis(2-pyridylmethyl)-1,2-bipyrrolidine ligands are prepared by lit-erature processes and their iron(II) complexes investigated in the cis-dihydroxylation of olefins. For the first time, a synthetic nonheme iron catalyst shows enantioselectiv-ities comparable with those obtained with the osmium-based AD mixes. — (SUZUKI, K.; OLDENBURG, P. D.; QUE*, L. J.; Angew. Chem., Int. Ed. 47 (2008) 10, 1887-1889; Dep. Chem., Univ. Minn., Minneapolis, MN 55455, USA; Eng.) — Kieslich

27- 041