| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5227924 | Tetrahedron | 2006 | 7 Pages |
Abstract
Construction of furo[3,4-c]pyran ring skeleton was achieved starting from the Baylis-Hillman adducts. The synthesis was carried out by the successive introduction of propargyl alcohol, radical cyclization, reduction, allylation, and finally ring-closing metathesis reaction.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Saravanan Gowrisankar, Ka Young Lee, Jae Nyoung Kim,
![First Page Preview: Construction of furo[3,4-c]pyran skeleton starting from the Baylis-Hillman adducts via the ring-closing metathesis (RCM) reaction of exo-methylene tetrahydrofuran Construction of furo[3,4-c]pyran skeleton starting from the Baylis-Hillman adducts via the ring-closing metathesis (RCM) reaction of exo-methylene tetrahydrofuran](/preview/png/5227924.png)