Process and intermediates for beta-lactam antibiotics

Details Process and intermediates for beta-lactam antibiotics Process and intermediates for beta-lactam antibiotics

1987-02-11

1988-03-29

Berch, Mark L.

Organic compounds -- part of the class 532-570 series

Organic compounds

Unsubstituted hydrocarbyl chain between the ring and the -c-...

C07D20508, C07D41304, C07D41314, C07D40914

Patent

active

047344954

ABSTRACT:
1-Benzyl(or substituted benzyl)-3.beta.-[4(S)-aryloxazolidin-2-one-3-yl]-4.beta.-(2-arylvinyl)azet idin-2-ones are provided via cycloaddition of a 4(S)-aryloxazolidin-2-one-3-ylacetyl halide and an imine formed with a benzylamine and a 3-arylacrolein, e.g. cinnamaldehyde. The azetidinones are useful chiral intermediates in an asymmetric synthesis of 1-carba(1-dethia)-3-hydroxy-3-cephem-4-carboxylic acids and esters and to monocyclic .beta.-lactam antibiotics.

REFERENCES:
Evans, Tet Letters, 26, 3787-90, (1985).

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