Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Anna C. Dawsey"'
Autor:
Travis J. Williams, Buddhima N. Siriwardena-Mahanama, Xinping Wu, Matthew J. Allen, Anna C. Dawsey
Publikováno v:
Journal of Fluorine Chemistry. 168:177-183
Responsive magnetic resonance imaging (MRI) contrast agents, those that change their relaxivity according to environmental stimuli, have promise as next generation imaging probes in medicine. While several of these are known based on covalent modific
Autor:
Justine A. Pardi, R. Brent Dixon, Jaime R. Swartzwelder, Karen E. Gebhardt, Ruth M. Labardee, Steven W. Cotten, Anna C. Dawsey
Publikováno v:
Clinical biochemistry. 50(18)
Objective Neonatal abstinence syndrome (NAS) is a rising concern with unknown long-term effects. It is apparent that higher cost of care, impact on the community and reduced quality of life are associated with similar etiologies ( e.g. , fetal alcoho
Autor:
Kevin J. Bigham, Jordan B. Brown, William T. Pennington, Anna C. Dawsey, Clyde R. Metz, John D. Knight, Don VanDerveer, Charles F. Beam
Publikováno v:
Journal of Chemical Crystallography. 40:296-301
Dilithiated C(α), N-carbomethoxyhydrazones were condensed with lithiated methyl 2-(aminosulfonyl)benzoate to afford intermediates that were isolated and not characterized but cyclized with acetic anhydride, which also resulted in N-acetylation. The
Autor:
Don VanDerveer, Anna C. Dawsey, Clyde R. Metz, Andrew J. Puciaty, Chandra Potter, Ellyn A. Smith, Amanda M. Acevedo-Jake, Charles F. Beam, William T. Pennington, Zachary C. Kennedy, John D. Knight
Publikováno v:
Journal of Heterocyclic Chemistry. 46:231-236
A variety of substituted spiro(benzoisothiazole-pyrazoles) have been prepared by the condensation of dilithiated C(α),N-carboalkoxyhydrazones with lithiated methyl 2-(aminosulfonyl)benzoate followed by the cyclization of intermediates with acetic an
Publikováno v:
Synthetic Communications. 38:4150-4159
Select C(α),N-phenylhydrazones were dilithiated with excess lithium diisopropylamide to their dianion-type intermediates followed by condensation with methyl hydrogen phthalate. The resulting C-acylated hydrazones were not isolated but acid cyclized
Publikováno v:
Dalton transactions (Cambridge, England : 2003). 41(26)
We report herein convenient, aerobic conditions for the oxidation of thiazolines to thiazoles and data regarding the oxidation mechanism. These reactions feature operationally simple and environmentally benign conditions and proceed in good yield to
Publikováno v:
ChemInform. 40
Select C(α),N-phenylhydrazones were dilithiated with excess lithium diisopropylamide to their dianion-type intermediates followed by condensation with methyl hydrogen phthalate. The resulting C-acylated hydrazones were not isolated but acid cyclized