Yadav, J. S. ; Subba Reddy, B. V. ; Narayana Kumar, G. G. K. S. ; Swamy, T. (2007) Iodine as a versatile reagent for the Prins-cyclization: an expeditious synthesis of 4-iodotetrahydropyran derivatives Tetrahedron Letters, 48 (12). pp. 2205-2208. ISSN 0040-4039
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Official URL: http://www.sciencedirect.com/science/article/pii/S...
Related URL: http://dx.doi.org/10.1016/j.tetlet.2007.01.076
Abstract
Iodine is found to be an efficient reagent for the coupling of homoallylic alcohols with aldehydes under mild conditions to produce 4-iodotetrahydropyran derivatives in excellent yields in a short reaction time with high selectivity. The use of iodine makes this procedure simple, convenient and cost-effective.
| Item Type: | Article |
|---|---|
| Source: | Copyright of this article belongs to Elsevier Science. |
| Keywords: | Prins-cyclization; Molecular Iodine; Homoallylic Alcohol; 4-iodopyrans |
| ID Code: | 58800 |
| Deposited On: | 02 Sep 2011 03:25 |
| Last Modified: | 02 Sep 2011 03:25 |
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