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The PMe3-catalyzed addition of enantiomerically pure (-)-MenthylO (Ph)P(O)H to electron-deficient alkenes: an efficient way for the preparation of P-stereogenic compounds

Journal

TETRAHEDRON-ASYMMETRY
Volume 28, Issue 1, Pages 84-89

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.tetasy.2016.11.005

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Funding

  1. Grants-in-Aid for Scientific Research [16K14049] Funding Source: KAKEN

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A variety of P-stereogenic organophosphorus compounds can be readily prepared by stereoretentive addition. The PMe3-catalyzed addition of optically active (-)MenthylO(Ph)P(O)H compounds to electron deficient alkenes occur stereospecifically, to produce the corresponding P-stereogenic adducts in high yields. By simply removing the volatiles under vacuum, spectroscopically pure products can be obtained. The present method provides a salt-free clean process for the preparation of P-chiral organophosphorus compounds. (C) 2016 Elsevier Ltd. All rights reserved,

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