X=Y-ZH compounds as potential 1,3-dipoles. Part 43. Metal ion catalysed asymmetric 1,3-dipolar cycloaddition reactions of imines and menthyl acrylate

DOI: 10.1016/0040-4020(94)00940-V

Source and publish data:

Tetrahedron p. 273 - 294 (1995)

Update date:2022-08-03

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Authors:

Barr, Darrin A.

Dorrity, Michael J.

Grigg, Ronald

Hargreaves, Simon

Malone, John F.

Montgomery, John

Redpath, James

Stevenson, Paul

Thornton-Pett, Mark

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Article abstract of DOI:10.1016/0040-4020(94)00940-V

Metallo-azomethine ylides, generated from imines by the action of amine bases in combination with LiBr or AgOAc, undergo cycloaddition with both 1R, 2S, 5R- and 1S, 2R, 5S-menthyl acrylates at room temperature to give homochiral pyrrolidines in excellent

Full text of DOI:10.1016/0040-4020(94)00940-V

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