Carbonyl allylations by allylic chlorides utilizing a reduction of tin(IV) iodide to triiodostannate(II) species with iodide sources
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference25 articles.
1. AN EFFICIENT METHOD FOR THE PREPARATION OF HOMOALLYLIC ALCOHOL DERIVATIVES BY THE REACTION OF ALLYL IODIDE WITH CARBONYL COMPOUNDS IN THE PRESENCE OF STANNOUS HALIDE
2. Allylbutyltin halides (CH2CHCH2)SnBu3−nCln (n = 0, 1, 2, 3). Preparation, carbon-13 NMR characterization and allylstannylation ability towards ketones and aldehydes
3. A simple, stereoselective, room-temperature synthesis of cis vinyloxiranes and trans 1-phenyl-1,3-butadiene
4. Tin(II)-aluminum-promoted allylation of aldehydes with allyl chloride in an aqueous solvent system
5. Stereocontrolled [m + n] annulation reactions. A [3 + 2] cycloaddition of 3-iodo-2-[(trimethylsilyl)methyl]propene onto 1,2-diones
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1. Making and Breaking of Sn−C and In−C Bonds in Situ: The Cases of Allyltins and Allylindiums;Chemical Reviews;2010-04-14
2. Tin(IV) Iodide;Fieser and Fieser's Reagents for Organic Synthesis;2009-12-15
3. Tetrabutylammonium Iodide;Encyclopedia of Reagents for Organic Synthesis;2008-09-15
4. Regio- and Diastereoselective Three-Component Syntheses of Homoallylic Amines in Aqueous Media Catalyzed by Brønsted Acids;European Journal of Organic Chemistry;2007-04
5. Aldol Reactions of α-Bromoalkyl Phenyl Ketones and Aldehydes with Tin(IV) Iodide and Tetrabutylammonium Iodide;Synlett;2006-11-23
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