| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5269749 | Tetrahedron Letters | 2011 | 4 Pages |
Abstract
Cyclohexanones react with phenylacetylene in a KOH/DMSO suspension (80 °C, 1 h) to give unexpectedly phenylmethylidene dispirocyclic ketals, 15-[(Z)-phenylmethylidene]-7,14-dioxadispiro[5.1.5.2]pentadecanes, in 16-22% yields (along with the anticipated β,γ- and α,β-ethylenic ketones).
Keywords
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Elena Yu Schmidt, Nadezhda V. Zorina, Elena V. Skitaltseva, Igor A. Ushakov, Albina I. Mikhaleva, Boris A. Trofimov,
![First Page Preview: 15-[(Z)-Phenylmethylidene]-7,14-dioxadispiro[5.1.5.2]pentadecanes: stereoselective one-pot assembly from cyclohexanones and phenylacetylene in a KOH/DMSO suspension 15-[(Z)-Phenylmethylidene]-7,14-dioxadispiro[5.1.5.2]pentadecanes: stereoselective one-pot assembly from cyclohexanones and phenylacetylene in a KOH/DMSO suspension](/preview/png/5269749.png)