| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5277571 | Tetrahedron Letters | 2006 | 4 Pages |
Abstract
The Prins-type cyclization of ketones with homoallylic and homopropargylic alcohols in the presence of TMSI generated in situ from TMSCl and NaI produced 2,2-disubstituted- or spirocyclic-4-iodo-tetrahydropyrans and spirocyclic-4-iodo-5,6-dihydro-2H-pyrans in good yields. These iodopyrans are reported for the first time.
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Authors
Gowravaram Sabitha, K. Bhaskar Reddy, M. Bhikshapathi, J.S. Yadav,