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2000
Volume 13, Issue 9
  • ISSN: 1385-2728
  • E-ISSN: 1875-5348

Abstract

Intramolecular haloetherification and transannular hydroxycyclization of alkenes is a synthetic methodology to obtain polycyclic ethers and amines in a regio- and stereoselective manner. The stereoelectronic effects controlling this selectivity are discussed. Also, the methodology based on [4+3]-cycloaddition followed by intramolecular haloetherification or transannular hydroxycyclization is described as a very useful tool to prepare the dioxa- and oxazatricyclic cores of several bioactive natural products, whose molecular scaffold is quite difficult to reach by other synthetic approaches.

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/content/journals/coc/10.2174/138527209788452135
2009-06-01
2025-05-02
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