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2000
Volume 5, Issue 6
  • ISSN: 1570-1786
  • E-ISSN: 1875-6255

Abstract

A variety of TBDMS ethers were directly transprotected into their acetates/benzoates with acetyl chloride/ benzoyl chloride in a one-pot procedure using CuBr2 (30 mol%). Chemo-selective transprotection of aliphatic TBDMS ethers in the presence of aromatic TBDMS ethers was achieved using 10 mol% of the catalyst. Various sensitive functional groups such as ketals, ketones, alkenes, allyl and benzyl ethers were found to be compatible under the reaction conditions.

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/content/journals/loc/10.2174/157017808785740543
2008-09-01
2025-09-06
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/content/journals/loc/10.2174/157017808785740543
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  • Article Type:
    Research Article
Keyword(s): acetates; benzoates; chemoselectivity; copper(II) bromide; TBDMS ethers; transprotection
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