| 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)