Complex Pyrrolidines via a Tandem Michael Reaction/1,3-Dipolar Cycloaddition Sequence. A Novel Method for the Generation of Unsymmetrical Azomethine Ylides

DOI: 10.1021/jo00289a005

Source and publish data:

Journal of Organic Chemistry p. 412 - 414 (1990)

Update date:2022-08-04

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Authors:

Garner, Philip

Arya, Fariba

Ho, Wen-Bin

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Article abstract of DOI:10.1021/jo00289a005

A novel tandem Michael addition/1,3-dipolar cycloaddition protocol for the assembly of the 3,8-diazabicyclo<3.2.1>octane ring system found in naphthyridinomycin (1) and quinocarcin (2) is described.

Full text of DOI:10.1021/jo00289a005

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