All Outputs (3)

N-(Alkylsulfamoyl)aldimines: easily deprotected precursors for diarylmethylamine synthesis (2013)
Journal Article
Crampton, R. H., Fox, M., & Woodward, S. (2013). N-(Alkylsulfamoyl)aldimines: easily deprotected precursors for diarylmethylamine synthesis. Tetrahedron: Asymmetry, 24(9-10), https://doi.org/10.1016/j.tetasy.2013.04.006

ZrCl₂(η-C₅Me₅)₂-AlHCl₂•(THF)₂: efficient hydroalumination of terminal alkynes and cross-coupling of the derived alanes (2013)
Journal Article
Andrews, P., Latham, C. M., Magre, M., Willcox, D., & Woodward, S. (2013). ZrCl₂(η-C₅Me₅)₂-AlHCl₂•(THF)₂: efficient hydroalumination of terminal alkynes and cross-coupling of the derived alanes. Chemical Communications, 49(15), https://doi.org/10.1039/C2CC37537K

On DABAL-Me₃ promoted formation of amides (2013)
Journal Article
Dubois, N., Glynn, D., Mcinally, T., Rhodes, B., Woodward, S., Irvine, D., & Dodds, C. (2013). On DABAL-Me₃ promoted formation of amides. Tetrahedron, 69(46), https://doi.org/10.1016/j.tet.2013.08.062

The range and utility of DABAL-Me3 couplings of methyl esters and free carboxylic acids with primary and secondary amines under a variety of conditions (reflux, sealed tube, microwave) has been compared for a significant range of coupling partners of... Read More about On DABAL-Me₃ promoted formation of amides.