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2000
Volume 10, Issue 1
  • ISSN: 1570-1786
  • E-ISSN: 1875-6255

Abstract

Under Mitsunobu conditions N-Boc-2-(hydroxymethyl)piperidine acts as a source of tert-butyl residue for the conversion of phenols into aryl tert-butyl ethers under neutral conditions. This reactivity can be attributed to a neighboring group contribution which strongly depends on the structure of the employed N-Boc-aminoalcohol. Five other, closely related N-Boc-aminoalcohols investigated here did not show this special reactivity, and gave the regular Mitsunobu coupling products.

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/content/journals/loc/10.2174/157017813805077253
2013-01-01
2025-09-08
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