| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5287575 | Tetrahedron Letters | 2007 | 4 Pages |
Abstract
SmI2-induced reductive cyclization of (E)- and (Z)-β-alkoxyvinyl sulfones with aldehyde stereoselectively afforded 2,6-syn-2,3-trans- and 2,6-syn-2,3-cis-tetrahydropyrans, respectively. The product having a sulfonylmethyl group was converted to a cyclic ether having a methyl group by reduction with Raney-Ni.
Related Topics
Physical Sciences and Engineering
Chemistry
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Authors
Tomohiro Kimura, Tadashi Nakata,