Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Kimberly A. Strauss"'
Publikováno v:
Tetrahedron Letters. 44:4321-4325
Microwave heating of high-loading TEMPO-methyl resin with functionalized styrenyl monomers in a SmithSynthesizer™ affords larger resin beads (>500 μm) via living free radical polymerization. Novel, high-loading Rasta resins (>5.5 mmol/g) are obtai
Publikováno v:
Tetrahedron Letters. 43:6319-6323
The synthesis of fluorous-tethered amine bases is described. These novel fluorous-tethered reagents promote reactions, remove acidic by-products, and scavenge electrophiles. They are readily separated from the reaction mixture by solid phase extracti
Publikováno v:
ChemInform. 33
The Staudinger reaction has been adapted for parallel synthesis by the application of fluorous-tethered triphenyl phosphine. The fluorous-tethered triphenylphosphine is expediently removed in parallel by Fluoro Flash ™ SPE columns to afford functio
Publikováno v:
ChemInform. 33
The synthesis of fluorous-tethered amine bases is described. These novel fluorous-tethered reagents promote reactions, remove acidic by-products, and scavenge electrophiles. They are readily separated from the reaction mixture by solid phase extracti
Autor:
Michael B. Grossman, Lisa M. Gaffney, Patricia A. Mars, Kimberly A. Strauss, Meryl O. Daly-Parker, Louise D Jakubik
Publikováno v:
Journal for specialists in pediatric nursing : JSPN. 9(4)
ISSUES AND PURPOSE. The development of a multiunit-based certificate program to promote retention by increasing experienced pediatric nurses' knowledge, skills, and professional role development through a blend of didactic, clinical, and mentoring co
Publikováno v:
Journal of combinatorial chemistry. 5(3)
Solution-phase parallel synthesis has had a profound impact on the speed of compound synthesis delivering relatively pure compounds (80%) in short order. However, to develop structure activity relationships (SAR) for a compound series, each library m
Publikováno v:
ChemInform. 34
By the application of microwave technology, a general protocol has been developed for the rapid synthesis of diverse 3,5,6-trisubstituted 1,2,4-triazines in excellent yield and purity, including many previously unknown 3-heterocyclic-1,2,4-triazines.