Yadav, J. S. ; Subba Reddy, B. V. ; Jayasudhan Reddy, Y. ; Sivasankar Reddy, N. (2009) Three-component synthesis of 2-aryl-4-arylthio-tetrahydro-2H-pyrans via the Prins-cyclization Tetrahedron Letters, 50 (24). pp. 2877-2880. ISSN 0040-4039
Full text not available from this repository.
Official URL: http://www.sciencedirect.com/science/article/pii/S...
Related URL: http://dx.doi.org/10.1016/j.tetlet.2009.03.176
Abstract
A three-component coupling of aldehyde, homoallylic alcohol and aryl thiol has been achieved in the presence of trifluoroacetic acid in dichloromethane at room temperature to produce 4-arylthiotetrahydropyrans in good yields with all cis-selectivity. This method is simple, selective and convenient for introducing a thiol group on a tetrahydropyran ring.
| Item Type: | Article |
|---|---|
| Source: | Copyright of this article belongs to Elsevier Science. |
| Keywords: | Prins-cyclization; Three-component Reaction; 4-arylthiotetrahydropyrans |
| ID Code: | 58752 |
| Deposited On: | 02 Sep 2011 03:33 |
| Last Modified: | 02 Sep 2011 03:33 |
Repository Staff Only: item control page
