4.4 Article

RCM strategy-based entry into new crown ether/polyether macrocyclic systems derived from hydroxy benzaldehydes

Journal

TETRAHEDRON LETTERS
Volume 54, Issue 18, Pages 2255-2260

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.tetlet.2013.02.072

Keywords

Crown ethers; Epoxide functionality; Grubbs's catalyst; Hydroxy ketone functionality; Macrocycles; Ring closing metathesis

Funding

  1. IISER-Mohali
  2. CSIR/UGC, New Delhi

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Entry into the 16-24 membered new crown ether/polyether macrocyclic molecules and the post ring-closure functional derivatization/periphery modification of polyether macrocyclic systems are reported. The synthesis of the epoxide, alpha-hydroxy ketone and olefinic functionality installed crown ether/polyether macrocyclic molecules was accomplished using the ring closing metathesis (RCM), epoxidation, oxidation and catalytic hydrogenation-based synthetic transformations starting from various hydroxy benzaldehydes. (C) 2013 Elsevier Ltd. All rights reserved.

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