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Please use this identifier to cite or link to this item: https://doi.org/10.1016/j.tetlet.2009.07.020
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dc.titleA mild method for the protection of alcohols using a para-methoxybenzylthio tetrazole (PMB-ST) under dual acid-base activation
dc.contributor.authorKotturi, S.R.
dc.contributor.authorTan, J.S.
dc.contributor.authorLear, M.J.
dc.date.accessioned2014-06-23T05:30:27Z
dc.date.available2014-06-23T05:30:27Z
dc.date.issued2009-09-16
dc.identifier.citationKotturi, S.R., Tan, J.S., Lear, M.J. (2009-09-16). A mild method for the protection of alcohols using a para-methoxybenzylthio tetrazole (PMB-ST) under dual acid-base activation. Tetrahedron Letters 50 (37) : 5267-5269. ScholarBank@NUS Repository. https://doi.org/10.1016/j.tetlet.2009.07.020
dc.identifier.issn00404039
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/75445
dc.description.abstractWith 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). © 2009 Elsevier Ltd. All rights reserved.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1016/j.tetlet.2009.07.020
dc.sourceScopus
dc.typeArticle
dc.contributor.departmentCHEMISTRY
dc.description.doi10.1016/j.tetlet.2009.07.020
dc.description.sourcetitleTetrahedron Letters
dc.description.volume50
dc.description.issue37
dc.description.page5267-5269
dc.description.codenTELEA
dc.identifier.isiut000269051700028
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