The asymmetric synthesis of 2,3-benzocarbapenems by intramolecular aryl radical cyclizations

DOI: 10.1016/0957-4166(96)00271-6

Source and publish data:

Tetrahedron Asymmetry p. 2203 - 2206 (1996)

Update date:2022-08-03

Topics:

Authors:

Alcaide, Benito

Moreno, Angel M.

Rodriguez-Vicente, Alberto

Sierra, Miguel A.

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Article abstract of DOI:10.1016/0957-4166(96)00271-6

Racemic and enantiomerically pure 2,3-benzocarbapenems 1 are obtained in good yields by the tin-mediated, intramolecular aryl radical cyclizations of the readily available 4-alkenyl-N-(2-halogenophenyl)-β-lactams 2.

Full text of DOI:10.1016/0957-4166(96)00271-6

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