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Stereospecific Radical Polymerization of N-Triphenylmethylmethacrylamides Leading to Highly Isotactic Helical Polymers
American Chemical Society | 2003| -
Structural Analysis of Amylose Tris(3,5-dimethylphenylcarbamate) by NMR Relevant to Its Chiral Recognition Mechanism in HPLC
American Chemical Society | 2002| -
Chromatographic resolution. 7. Useful chiral packing materials for high-performance liquid chromatographic resolution of enantiomers: phenylcarbamates of polysaccharides coated on silica gel
National licenceAmerican Chemical Society | 1984| -
NMR Studies of Chiral Discrimination Relevant to the Liquid Chromatographic Enantioseparation by a Cellulose Phenylcarbamate Derivative
American Chemical Society | 1996| -
Resolution of racemic compounds by optically active poly(triphenylmethyl methacrylate)
National licenceAmerican Chemical Society | 1980| -
Poly((4-carboxyphenyl)acetylene) as a Probe for Chirality Assignment of Amines by Circular Dichroism
National licenceAmerican Chemical Society | 1995| -
Asymmetric polymerization of triphenylmethyl methacrylate leading to a one-handed helical polymer: mechanism of polymerization
National licenceAmerican Chemical Society | 1992| -
Efficient Lewis Acid-Catalyzed Stereocontrolled Radical Polymerization of Acrylamides
American Chemical Society | 2001| -
Dibenzofulvene, a 1,1-Diphenylethylene Analogue, Gives a π-Stacked Polymer by Anionic, Free-Radical, and Cationic Catalysts
American Chemical Society | 2001|
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