THE STEREOCONTROLLED SYNTHESIS OF VERSATILE CARBAPENEM INTERMEDIATES USING THE BARTON O-ACYL 2-THIOPYRIDYLHYDROXAMATE FRAGMENTATION

DOI: 10.1016/S0040-4039(00)77706-9

Source and publish data:

Tetrahedron Letters p. 749 - 752 (1992)

Update date:2022-09-26

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Authors:

Sumi, Kenzo

Fabio, Romani Di

Hanessian, Stephen

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Article abstract of DOI:10.1016/S0040-4039(00)77706-9

The photo-initiated fragmentation of 2-azetidinone-4-carboxylic acid 2-thiopyridylhydroxamates (Barton reaction) in the presence of Michael acceptors leads to the introduction of a doubly functionalized carbon chain, useful for the elaboration of carbapenem and related β-lactam antibiotics.

Full text of DOI:10.1016/S0040-4039(00)77706-9

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