Jerald S Bradshaw
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Explore the profile of Jerald S Bradshaw including associated specialties, affiliations and a list of published articles.
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13
Citations
34
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Recent Articles
1.
Habata Y, Okazaki C, Ogura K, Akabori S, Zhang X, Bradshaw J
Inorg Chem
. 2007 Sep;
46(20):8264-70.
PMID: 17784752
Structures of LiSCN, NaSCN, KSCN, RbSCN, and CsSCN complexes with 3',5'-difluoro-4'-hydroxybenzyl-armed monoaza-15-crown-5 ether (5) were investigated. The Li+ and Na+ complexes are (1:1)n polymer-like complexes bridged by hydrogen bonding. On...
2.
Bronson R, Michaelis D, Lamb R, Husseini G, Farnsworth P, Linford M, et al.
Org Lett
. 2005 Mar;
7(6):1105-8.
PMID: 15760150
[reaction: see text] The development of an ion-selective chemosensor for Cd(2+) allows generation of a "real-time" sensor. Immobilization of the chemosensor on quartz was achieved in a simple monolayer and...
3.
Gong Y, Xiang Y, Yue B, Xue G, Bradshaw J, Lee H, et al.
J Chromatogr A
. 2003 Jul;
1002(1-2):63-70.
PMID: 12885079
Two bonded chiral stationary phases (CSPs), 8-aminoquinoline-2-ylmethyl- and 8-aminoquinoline-7-ylmethyl-diaza-18-crown-6-capped [3-(2-O-beta-cyclodextrin)-2-hydroxypropoxy]propylsilyl silica particles (non-porous, 1.5 microm), have been prepared and evaluated using capillary liquid chromatography at high pressures (> or =...
4.
Juvanc Z, Markides K, Petersson P, Johnson D, Bradshaw J, Lee M
J Chromatogr A
. 2002 Dec;
982(1):119-26.
PMID: 12489861
A copolymeric stationary phase, consisting of a chiral selective part, i.e. (1R-trans)-N,N'-1,2-cyclohexylenebisbenzamide, and an efficient siloxane oligomeric part, was successfully applied to open tubular column GC analysis. The efficiency and...
5.
Zhang X, Bradshaw J, Izatt R
Chem Rev
. 2002 Feb;
97(8):3313-3362.
PMID: 11851492
No abstract available.
6.
Su N, Bradshaw J, Zhang X, Song H, Savage P, Xue G, et al.
J Org Chem
. 2001 Oct;
64(24):8855-8861.
PMID: 11674789
Ten new 8-hydroxyquinoline-containing diaza-18-crown-6 ligands and analogues were synthesized via a one-pot or stepwise Mannich reaction, reductive amination, or by reacting diaza-18-crown-6 with 5,7-dichloro-2-iodomethyl-8-quinolinol in the presence of N,N-diisopropylethylamine. The...
7.
Yang Z, Bradshaw J, Zhang X, Savage P, Krakowiak K, Dalley N, et al.
J Org Chem
. 2001 Oct;
64(9):3162-3170.
PMID: 11674416
A series of macrocyclic tetraazacrown ethers containing two pyridine, quinoline, 8-hydroxyquinoline, or 8-aminoquinoline sidearms has been prepared. Crab-like cyclization of bis(alpha-chloroacetamide)s and diamines followed by reduction of the cyclic diamides...
8.
Chen Z, Bradshaw J, Shen Y, Habata Y, Lee M
J Org Chem
. 2001 Oct;
62(24):8529-8534.
PMID: 11671996
Natural beta-cyclodextrin was treated with 3.5 equiv of tert-butyldimethylsilyl chloride and then with NaH and MeI in the same reaction vessel to give a mixture of oligosilyl-substituted permethylated beta-cyclodextrins. The...
9.
Pastushok V, Hu K, Bradshaw J, Dalley N, Bordunov A, Lukyanenko N
J Org Chem
. 1997 Jan;
62(1):212-215.
PMID: 11671386
No abstract available.
10.
Chen Z, Bradshaw J, Yi G, Pyo D, Black D, Zimmerman S, et al.
J Org Chem
. 1996 Dec;
61(25):8949-8955.
PMID: 11667876
The syntheses, structures, and spectroscopic properties of 6(A),6(B)-bis-O-[p-(allyloxy)phenyl]-substituted beta-cyclodextrins have been investigated. Selective activation of the 6(A),6(B)-hydroxy groups was carried out by treating heptakis(2,3-di-O-methyl)-beta-cyclodextrin (1) with 2,4-dimethoxybenzene-1,5-disulfonyl chloride to give...