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A strategy based on the use of homo bi-and multifunctional building blocks for the synthesis of a new class of network-polymeric chiral stationary phases has been evaluated. The key steps comprise acylation of N,N'-diallyl-L-tartardiamide (DATD) and reaction with a multifunctional hydrosilane, yield
on the occasion of his 60th birthduy Many biologically active substances are now tested in their enantiomerically pure form. Chiral stationary phases (CSPs) can ensure not only reliable enantiomer analysis but also ready availability of the two enantiomers of a racemic active substance at a very ear
Molecule imprinting polymers (MIPs) with high chiral selectivity for N a -protected amino acids were synthesized in polar solvent using acrylamide (AM) or combined functional monomer methacrylic acid (MAA) vinyl pyridine (VP). Factors that influence the chiral selectivity of MIPs and mechanisms of t
## Abstract Two chiral stationary phases derived from derivatized amylose (Chiralpak ADβH and Chiralpak IA) have been used to separate the enantiomers of new diethyl benzamidoarylmethylphosphonates. The data obtained indicate that all the studied compounds could be easily baseline resolved on both