1. ScholarBank@NUS
  2. 1. Staff
  3. Staff Publications
Please use this identifier to cite or link to this item: https://doi.org/10.1016/j.tetlet.2007.09.078
DC FieldValue
dc.titleIodobenzene-catalysed iodolactonisation using sodium perborate monohydrate as oxidant
dc.contributor.authorLiu, H.
dc.contributor.authorTan, C.-H.
dc.date.accessioned2014-06-23T05:42:21Z
dc.date.available2014-06-23T05:42:21Z
dc.date.issued2007-11-12
dc.identifier.citationLiu, H., Tan, C.-H. (2007-11-12). Iodobenzene-catalysed iodolactonisation using sodium perborate monohydrate as oxidant. Tetrahedron Letters 48 (46) : 8220-8222. ScholarBank@NUS Repository. https://doi.org/10.1016/j.tetlet.2007.09.078
dc.identifier.issn00404039
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/76403
dc.description.abstractA convenient approach has been developed for iodolactonisation using iodobenzene as catalyst. The active reagent was generated in situ with tetra-n-butylammonium iodide (TBAI) and hypervalent iodine reagent, diacetoxyiodobenzene (PIDA). PIDA, in turn, was generated in situ using a catalytic amount of iodobenzene with sodium perborate monohydrate as the stoichiometric oxidant. A variety of olefinic acids including δ-pentenoic acids, δ-pentynoic acids and δ-hexynoic acid gave high yields of lactones using this methodology. © 2007 Elsevier Ltd. All rights reserved.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1016/j.tetlet.2007.09.078
dc.sourceScopus
dc.typeArticle
dc.contributor.departmentCHEMISTRY
dc.description.doi10.1016/j.tetlet.2007.09.078
dc.description.sourcetitleTetrahedron Letters
dc.description.volume48
dc.description.issue46
dc.description.page8220-8222
dc.description.codenTELEA
dc.identifier.isiut000252097100032
Appears in Collections:Staff Publications

Show simple item record
Files in This Item:
There are no files associated with this item.

Google ScholarTM

Check

Altmetric


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.