The Journal of Organic Chemistry · 1996 · 36 citations · 23 references
Natural SciencesChemistryCatalysisGreen ChemistryOrganic ChemistryCross-coupling ReactionsHeterocycle SynthesisOrganic SynthesisRetrosynthetic AnalysisAllylic FunctionalizationAsymmetric SynthesisStereoselective Cross-couplingStereoselective Reaction DesignStereoselective SynthesisX-ray Diffraction AnalysisX-ray Structure Determination
A series of allyl bromides bearing an ethereal stereogenic substituent at C-2 were synthesized from methyl acrylate. These were coupled with a range of aldehydes under chromium(II) chloride-mediated conditions to afford syn-4-alkoxyalkan-1-ols in good yield and diastereoselectivity. The effect of altering the nature of the ethereal group and alkyl substituent upon the diastereoselectivity of the reaction was also investigated. The relative stereochemistry was proved by X-ray structure analysis. The work was extended to replace the chromium(II) chloride with indium metal, and this also afforded syn-4-alkoxyalkan-1-ols in good yield and diastereoselectivity.
23
Purification of Laboratory Chemicals
Colin Eaborn · Journal of Organometallic Chemistry · 1989 · 4.4K citations
N-methoxy-n-methylamides as effective acylating agents
Steven Nahm, Steven M. Weinreb · Tetrahedron Letters · 1981 · 1.8K citations