Please use this identifier to cite or link to this item:
https://doi.org/10.1016/j.tetlet.2008.05.013
Title: | Sodium nitrite (NaNO2) catalysed iodo-cyclisation of alkenes and alkynes using molecular oxygen |
Authors: | Liu, H. Pan, Y. Tan, C.-H. |
Issue Date: | 7-Jul-2008 |
Source: | 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 |
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. |
Source Title: | Tetrahedron Letters |
URI: | http://scholarbank.nus.edu.sg/handle/10635/94827 |
ISSN: | 00404039 |
DOI: | 10.1016/j.tetlet.2008.05.013 |
Appears in Collections: | Staff Publications |
Show full item record
Files in This Item:
There are no files associated with this item.
SCOPUSTM
Citations
6
checked on Mar 7, 2018
WEB OF SCIENCETM
Citations
6
checked on Mar 7, 2018
Page view(s)
40
checked on Apr 20, 2018
Google ScholarTM
Check
Altmetric
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.