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2003 Enantioselective syntheses Enantioselective syntheses O 0031 Extended Scope of Dirhodium(II)-Catalyzed Enantioselective Intramolecular 1,3-Dipolar Cycloadditions of Carbonyl Ylides with Alkene and Alkyne Dipolaro- philes. — Enantioselective intramolecular 1,3-dipolar cycloaddition of carbonyl ylides shows promising scope in terms of asymmetric induction yielding tricyclic products (II) and (IV) in up to 86% e.e. — (HODGSON*, D. M.; LABANDE, A. H.; PIERARD, F. Y. T. M.; Synlett 2003, 1, 59-62; Dyson Perrins Lab., Dep. Chem., Univ. Oxford, Oxford OX1 3QY, UK; Eng.) — Mais 15- 038

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Page 1: Extended Scope of Dirhodium(II)-Catalyzed Enantioselective Intramolecular 1,3-Dipolar Cycloadditions of Carbonyl Ylides with Alkene and Alkyne Dipolarophiles

2003 Enantioselective syntheses

Enantioselective synthesesO 0031 Extended Scope of Dirhodium(II)-Catalyzed Enantioselective Intramolecular

1,3-Dipolar Cycloadditions of Carbonyl Ylides with Alkene and Alkyne Dipolaro-philes. — Enantioselective intramolecular 1,3-dipolar cycloaddition of carbonyl ylides shows promising scope in terms of asymmetric induction yielding tricyclic products (II) and (IV) in up to 86% e.e. — (HODGSON*, D. M.; LABANDE, A. H.; PIERARD, F. Y. T. M.; Synlett 2003, 1, 59-62; Dyson Perrins Lab., Dep. Chem., Univ. Oxford, Oxford OX1 3QY, UK; Eng.) — Mais

15- 038

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1,3-Dipolar Cycloadditions of Diazo Compounds in the ...raineslab.com/sites/default/files/labs/raines/pdfs/Aronoff2016a.pdf · 1,3-Dipolar Cycloadditions of Diazo Compounds in the

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and Homoallylic Alcohols Building Blocks: Cycloadditions ...ccc.chem.pitt.edu/wipf/Current Literature/Anthony_1.pdf · A Modular Approach to Polyketide Building Blocks: Cycloadditions

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μ Acetato)Dirhodium(II) as Catalystslibres.uncg.edu/ir/uncg/f/T_Nile_HydrosilyationUsing_1979.pdf · Acetato)Dirhodium(II) as Catalysts By: Andrew J. Cornish, Michael F. Lappert,

[4+3] Cycloadditions and Their Application in Synthesisevans.rc.fas.harvard.edu/pdf/smnr_2005_Lawrence_Jonathan.pdf[4+3] Cycloadditions and Their Application in Synthesis X + X concerted

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chemlabs.princeton.educhemlabs.princeton.edu/macmillan/wp-content/uploads/sites/6/... · Cycloadditions: Woodward-Hoffman Rules Frontier orbital theory dictates non-4n+2 cycloadditions