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Thienamycin enolate-imine condensations

This method can be effectively applied to the preparation of /S-lactam compounds. The ester enolate-imine condensation approach to j8-lactam formation has been developed over the past decade. Thienamycin and related carbapenems have been the focus of particular attention because of their structural uniqueness and potent antibacterial activity. [Pg.181]


See other pages where Thienamycin enolate-imine condensations is mentioned: [Pg.925]    [Pg.925]    [Pg.565]    [Pg.587]    [Pg.925]    [Pg.361]    [Pg.926]    [Pg.926]    [Pg.926]   
See also in sourсe #XX -- [ Pg.925 ]

See also in sourсe #XX -- [ Pg.925 ]

See also in sourсe #XX -- [ Pg.925 ]




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Enol imines

Enol-imine

Enolate condensation

Enolates condensation

Imine condensations

Imine enolates

Imines enolates

Thienamycine

Thienamycins

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