Sequential 1,3-dipolar cycloaddition-palladium catalysed cyclisation. A powerful new tactical combination

DOI: 10.1016/S0040-4039(00)79667-5

Source and publish data:

Tetrahedron Letters p. 1359 - 1362 (1991)

Update date:2022-08-03

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Authors:

Grigg, Ronald

Coulter, Thomas

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Article abstract of DOI:10.1016/S0040-4039(00)79667-5

A new flexible tactical combination of a 1,3-dipolar cycloaddition of an in situ generated azomethine ylide followed by a palladium catalysed cyclisation is described. The two reactions can be carried out as a 1 pot procedure if desired. Four new stereoce

Full text of DOI:10.1016/S0040-4039(00)79667-5

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