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ChemInform 2010, 41, issue 14 © 2010 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim www.cheminform.wiley-vch.de Diastereoselective syntheses O 0031 DOI: 10.1002/chin.201014026 Allene Carboxylates as Dipolarophiles in Rh-Catalyzed Carbonyl Ylide Cycload- ditions. — Allene carboxylates (II) are successfully applied as dipolarophiles in car- bonyl ylide cycloaddition reaction. The reaction proceeds with high diastereofacial selectivity giving only two out of four possible diastereomers with a preference for the E,endo-isomer (III). — (ROUT, L.; HARNED*, A. M.; Chem. Eur. J. 15 (2009) 47, 12926-12928; Dep. Chem., Univ. Minn., Minneapolis, MN 55455, USA; Eng.) — Mischke 14- 026

ChemInform Abstract: Allene Carboxylates as Dipolarophiles in Rh-Catalyzed Carbonyl Ylide Cycloadditions

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Diastereoselective synthesesO 0031 DOI: 10.1002/chin.201014026

Allene Carboxylates as Dipolarophiles in Rh-Catalyzed Carbonyl Ylide Cycload-ditions. — Allene carboxylates (II) are successfully applied as dipolarophiles in car-bonyl ylide cycloaddition reaction. The reaction proceeds with high diastereofacial selectivity giving only two out of four possible diastereomers with a preference for the E,endo-isomer (III). — (ROUT, L.; HARNED*, A. M.; Chem. Eur. J. 15 (2009) 47, 12926-12928; Dep. Chem., Univ. Minn., Minneapolis, MN 55455, USA; Eng.) — Mischke

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ChemInform 2010, 41, issue 14 © 2010 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim