cheminform abstract: cycloaddition methodology. a useful entry towards biologically active...

ChemInform 2009, 40, issue 40 © 2009 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim www.cheminform.wiley-vch.de Organic chemistry Z 0200 Cycloaddition Methodology. A Useful Entry Towards Biologically Active Hetero- cycles — [84 refs.]. — (CHIACCHIO, U.; PADWA, A.; ROMEO, G.; Curr. Org. Chem. 13 (2009) 5, 422-447; Dip. Sci. Chim., Univ. Catania, I-95125 Catania, Italy; Eng.) — Meier 40- 232

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Page 1: ChemInform Abstract: Cycloaddition Methodology. A Useful Entry Towards Biologically Active Heterocycles

www.cheminform.wiley-vch.de

Organic chemistryZ 0200 Cycloaddition Methodology. A Useful Entry Towards Biologically Active Hetero-

cycles — [84 refs.]. — (CHIACCHIO, U.; PADWA, A.; ROMEO, G.; Curr. Org. Chem. 13 (2009) 5, 422-447; Dip. Sci. Chim., Univ. Catania, I-95125 Catania, Italy; Eng.) — Meier

40- 232

Enantioselective Cycloaddition Reactions Catalyzed by BINOL

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INTRODUCTION - UPV/EHU OF HETEROCYCLES Heterocycles can be classified intothreegeneral groups X Saturated Partially saturated Aromatic SATURATED HETEROCYCLES X=O: Oxane X=S: Thiane

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Cycloaddition Reactions of the Fulvenes

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