They are found as constituents of an increasing group of biologically active peptides. Stereocontrolled syntheses of chiral and racemic key intermediates to thienamycin from d-allo-threonine and trans-crotonic acid.
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Aplicaciones
Se encuentra como componentes de un grupo creciente de péptidos biológicamente activos. Stereocontrolled syntheses of chiral and racemic key intermediates to thienamycin from d-allo-threonine and trans-crotonic acid.
Solubilidad
Soluble en agua.
Notas
Almacenar en un lugar fresco. Mantenga el recipiente bien cerrado en un lugar seco y bien ventilado. Almacenar alejado de agentes oxidantes fuertes.
RUO – Research Use Only
General References:
- Peter Wipf,; Chris P. Miller. Stereospecific synthesis of peptide analogs with allo-threonine and D-allo-threonine residues . J. Org. Chem.. 1993, 58 (6),1575-1578.
- Masao Shiozaki,; Noboru Ishida,; Hiroshi Maruyama,; Tetsuo Hiraoka. Stereocontrolled syntheses of chiral and racemic key intermediates to thienamycin from d-allo-threonine and trans-crotonic acid. Tetrahedron. 1983, 39(14),2399-2407.