Please use this identifier to cite or link to this item:
https://doi.org/10.1016/j.tetlet.2008.05.013
DC Field | Value | |
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dc.title | Sodium nitrite (NaNO2) catalysed iodo-cyclisation of alkenes and alkynes using molecular oxygen | |
dc.contributor.author | Liu, H. | |
dc.contributor.author | Pan, Y. | |
dc.contributor.author | Tan, C.-H. | |
dc.date.accessioned | 2014-10-16T08:40:32Z | |
dc.date.available | 2014-10-16T08:40:32Z | |
dc.date.issued | 2008-07-07 | |
dc.identifier.citation | Liu, H., Pan, Y., Tan, C.-H. (2008-07-07). Sodium nitrite (NaNO2) catalysed iodo-cyclisation of alkenes and alkynes using molecular oxygen. Tetrahedron Letters 49 (28) : 4424-4426. ScholarBank@NUS Repository. https://doi.org/10.1016/j.tetlet.2008.05.013 | |
dc.identifier.issn | 00404039 | |
dc.identifier.uri | http://scholarbank.nus.edu.sg/handle/10635/94827 | |
dc.description.abstract | We have developed a convenient iodo-cyclisation reaction using NaNO2 as catalyst and molecular oxygen as the terminal oxidant. The reactive species, acetyl hypoiodite (IOAc), was generated in situ from TBAI and AcOH. The iodo-cyclisation reaction with a range of alkenes and alkynes gave good to excellent yields. Iodo-amination products can also be obtained using carbamates prepared from commercially available allylic alcohols and alkynic alcohols. © 2008 Elsevier Ltd. All rights reserved. | |
dc.description.uri | http://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1016/j.tetlet.2008.05.013 | |
dc.source | Scopus | |
dc.type | Article | |
dc.contributor.department | CHEMISTRY | |
dc.description.doi | 10.1016/j.tetlet.2008.05.013 | |
dc.description.sourcetitle | Tetrahedron Letters | |
dc.description.volume | 49 | |
dc.description.issue | 28 | |
dc.description.page | 4424-4426 | |
dc.description.coden | TELEA | |
dc.identifier.isiut | 000257194400027 | |
Appears in Collections: | Staff Publications |
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