Synthesis and Radical Polyaddition of Optically Active Monomers Derived from Cysteine
β Scribed by Kudo, Hiroto; Sanda, Fumio; Endo, Takeshi
- Book ID
- 127125912
- Publisher
- American Chemical Society
- Year
- 1999
- Tongue
- English
- Weight
- 146 KB
- Volume
- 32
- Category
- Article
- ISSN
- 0024-9297
No coin nor oath required. For personal study only.
π SIMILAR VOLUMES
The synthesis of three new stereoregular AB-type polyamides based on Dribono-1,4-lactone, L-arabinose, and D-xylose has been carried out by the active ester polycondensation method. These polyamides were characterized by elemental analysis, IR and NMR spectroscopies, and powder X-ray diffraction. Th
Syntheses and radical polymerizations of methacrylamides derived from optically active amino alcohols were carried out. The monomers were prepared by condensation of optically active amino alcohols and methacrylic acid using l-ethyl-3-(3-dimethylamino-propy1)carbodiimide hydrochloride (EDC -HCl). Ra