Use of aluminium as the reducing metal in spontaneous bimetal redox reaction has been elegantly exploited for allylation/crotylation of aldehydes in wet solvent. Here, low valent tin was prepared in situ by reduction of SnCl2 center dot 2H(2)O with aluminium in THF/water. The resulting low valent tin acted as an efficient mediator for allylation and crotylation of aldehydes (3a-q) producing the corresponding homoallylic alcohols. The efficacy of this procedure was due to its operational simplicity, practical viability, inexpensiveness, good yields of the products and short reaction time. (C) 2013 Elsevier Ltd. All rights reserved.
Regiospecific and highly stereoselective allylation of aldehydes with allyltrifluorosilane activated by fluoride ions.
作者:Mitsuo Kira、Mineo Kobayashi、Hideki Sakurai
DOI:10.1016/s0040-4039(01)83867-3
日期:1987.1
Carbonyl allylations by allylic chlorides utilizing a reduction of tin(IV) iodide to triiodostannate(II) species with iodide sources
Carbonylallylations by allylic chlorides either with tin(IV) iodide and tetrabutylammoniumiodide (TBAI) in dichloromethane or with tin(IV) iodide and sodium iodide in 1,3-dimethylimidazolidin-2-one at room temperature produced the corresponding homoallylic alcohols. The carbonylallylations probably proceeded via the reduction of tin(IV) iodide to triiodostannate(II) species with iodide sources such