Synfacts 2008(11): 1152-1152  
DOI: 10.1055/s-0028-1083491
Synthesis of Heterocycles
© Georg Thieme Verlag Stuttgart ˙ New York

Synthesis of 4-Azidotetrahydropyrans via Prins Cyclization

Contributor(s): Victor Snieckus, Timothy Hurst
J. S. Yadav*, B. V. S. Reddy, T. Maity, G. G. K. S. Narayana Kumar
Indian Institute of Chemical Technology, Hyderabad, India
Further Information

Publication History

Publication Date:
23 October 2008 (online)

Significance

The synthesis of all-cis 4-azidotetrahydropyrans 3 via the three-component coupling of aldehydes 1, homoallylic alcohols 2 and trimethylsilyl azide in the presence of phosphomolybdic acid (PMA) is described. The reaction is tolerant of a wide range of aldehydes bearing linear and branched aliphatic chains and electron-poor, -neutral and -rich aromatic groups. The acid-sensitive cinnamaldehyde was also found to participate well in the reaction. Furthermore, the coupling of substituted homoallylic alcohols was examined and found to proceed smoothly under the standard reaction conditions.