| Article ID | Journal | Published Year | Pages | File Type | 
|---|---|---|---|---|
| 5279791 | Tetrahedron Letters | 2006 | 4 Pages | 
Abstract
												A new and convenient procedure for the synthesis of homoallylic alcohols directly from aromatic acetals and dioxolanes has been developed with very good yields under biomimetic conditions using a Zn-mediated Barbier-type allylation in the presence of β-cyclodextrin in water.
											Related Topics
												
													Physical Sciences and Engineering
													Chemistry
													Organic Chemistry
												
											Authors
												K. Surendra, N. Srilakshmi Krishnaveni, K. Rama Rao, 
											