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A mild method for the protection of alcohols using a para-methoxybenzylthio tetrazole (PMB-ST) under dual acid–base activation

Version 2 2024-03-12, 13:22
Version 1 2024-03-01, 09:08
journal contribution
posted on 2024-03-12, 13:22 authored by Santosh R. Kotturi, Jason S. Tan, Martin LearMartin Lear
<p>With a view to expand the repertoire of chemoselective methods applicable to sensitive and multifunctional substrates, the p-methoxybenzylation of alcohols under essentially neutral conditions is reported. This was achieved by the silver triflate (AgOTf) activation of 5-(p-methoxybenzylthio)-1-phenyl-1H-tetrazole (PMB-ST) in the presence of 2,6-di-tert-butyl-4-methylpyridine (DTBMP).</p>

History

School affiliated with

  • School of Chemistry (Research Outputs)

Publication Title

Tetrahedron Letters

Volume

50

Issue

37

Pages/Article Number

5267-5269

Publisher

Elsevier

ISSN

0040-4039

Date Submitted

2015-04-16

Date Accepted

2009-07-03

Date of First Publication

2009-07-09

Date of Final Publication

2009-09-16

Date Document First Uploaded

2015-04-16

ePrints ID

17114

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