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1 ynthesis protocol is presented for accessing quaternized alpha-amino acids in chiral, nonracemic form
2                                          The quaternized analogues of the 2-chlorophenyl phenyl sulfi
3         The resulting 1-alkyl triazoles were quaternized at N-4 in >98% isolated yields using fluorin
4 orohydride reduction, furnishes alpha,alpha'-quaternized beta-hydroxypropionates in high ee overall.
5 c brushes swell to a greater extent than the quaternized brushes studied.
6 adienones featuring a key formyl group and a quaternized carbon atom in good yields.
7 s of the parent Mn(III)T-2-PyP(+) as do four quaternized cationic meso ortho pyridyl nitrogens.
8 lica deposition is confined to the partially quaternized cationic PDMA chains, leading to hybrid copo
9 f various dendrimer derivatives (acetylated, quaternized, etc.).
10       The quinoline groups do not have to be quaternized for blocking activity, as long as they are b
11 82% of the amine sites on the surface are in quaternized form.
12                The alkyl chain length in the quaternized nitrogen was shown to be fundamental for BSA
13 alkaline fuel cell applications, a series of quaternized poly(2,6-dimethyl phenylene oxide)s containi
14 jugate base of sulfanilic acid and then with quaternized poly(4-vinylpyridine).
15 ely 100 mum were prepared from triethylamine-quaternized-poly(vinylbenzyl chloride) cross-linked with
16             Based on two X-ray structures of quaternized products, the diastereoselectivity observed
17 kyl azides, and the resulting triazoles were quaternized providing well-defined multitriazolium platf
18 rivatives has been developed, furnishing C-3 quaternized pyrroloindoline architectures.
19 ibitory activities of an extensive series of quaternized quino[4,3,2- kl]acridinium salts against tum
20  the ability of the triblock comicelles with quaternized terminal segments to complex DNA and, thus,
21 ed from the rigid spatial arrangement of the quaternized triazole moieties above and below the Pc cor
22 Even though the ion exchange capacity of the quaternized trimethylaminated PSZrO2 (QTMA-PS-ZrO2) is o
23 iamino alkylene chain and the ring N atom is quaternized with a methyl or benzyl group.
24 droisoquinolines with aromatic aldehydes are quaternized with alkyl triflates and subsequently treate
25        Eight aminoalkylbacteriochlorins were quaternized with methyl iodide at two or four amine site
26  reaction was sluggish, the Mannich base was quaternized with methyl iodide which afforded much faste

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