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FERNANDO PALACIOS, MD
MD
Student in an Organized Health Care Education/Training Program
NPI: 1467296574Individual
Specialties, Licenses & Credentials
Student in an Organized Health Care Education/Training ProgramPrimary
Student in an Organized Health Care Education/Training Program
Code: 390200000X
Research & Publications (20)
Adsorptive stripping voltammetric determination of cefepime at the mercury electrode in human urine and cerebrospinal fluid, and differential pulse polarographic determination in serum.
PMID 12950003·J Pharm Sci·2003
8-other
Determination and identification, according to European Union Decision 2002/657/EC, of malachite green and its metabolite in fish by liquid chromatography-tandem mass spectrometry using an optimized extraction procedure and three-way calibration.
PMID 19535083·J Chromatogr A·2009
7-preclinical
Axonal mitochondrial clusters containing mutant SOD1 in transgenic models of ALS.
PMID 19344250·Antioxid Redox Signal·2009
7-preclinical
Reactions of conjugate phosphinyl- and phosphonyl-nitroso alkenes with enamines. Preparation of N-hydroxypyrrole derivatives.
PMID 19344164·J Org Chem·2009
8-other
Conjugate addition of amines to an alpha,beta-unsaturated imine derived from alpha-aminophosphonate. Synthesis of gamma-amino-alpha-dehydroaminophosphonates.
PMID 19053594·J Org Chem·2009
8-other
Synthesis of fluoroalkylated beta-aminophosphonates and pyridines from primary beta-enaminophosphonates.
PMID 18489181·J Org Chem·2008
8-other
Advantages of PARAFAC calibration in the determination of malachite green and its metabolite in fish by liquid chromatography-tandem mass spectrometry.
PMID 18313680·J Chromatogr A·2008
4-observational
A convenient synthesis of substituted pyrazolidines and azaproline derivatives through highly regio- and diastereoselective reduction of 2-pyrazolines.
PMID 18085795·J Org Chem·2008
8-other
Michael addition of amine derivatives to conjugate phosphinyl and phosphonyl nitrosoalkenes. Preparation of alpha-amino phosphine oxide and phosphonate derivatives.
PMID 17579451·J Org Chem·2007
8-other
Synthesis of alpha-phosphorylated alpha,beta-unsaturated imines and their selective reduction to vinylogous and saturated alpha-aminophosphonates.
PMID 17328577·J Org Chem·2007
8-other
Copper-catalyzed asymmetric conjugate addition of diethylzinc to alpha,beta-unsaturated imines derived from alpha-aminoacids. Enantioselective synthesis of gamma-substituted alpha-dehydroaminoesters.
PMID 17078729·Org Lett·2006
8-other
Efficient synthesis of 1-azadienes derived from alpha-aminoesters. Regioselective preparation of alpha-dehydroamino acids, vinylglycines, and alpha-amino acids.
PMID 16995675·J Org Chem·2006
8-other
Regioselective synthesis of fluoroalkylated beta-aminophosphorus derivatives and aziridines from phosphorylated oximes and nucleophilic reagents.
PMID 16872198·J Org Chem·2006
8-other
Reaction of N-vinylic phosphazenes with alpha,beta-unsaturated aldehydes. Azatriene-mediated synthesis of dihydropyridines and pyridines derived from beta-amino acids.
PMID 16872184·J Org Chem·2006
8-other
Straightforward access to pyrazines, piperazinones, and quinoxalines by reactions of 1,2-diaza-1,3-butadienes with 1,2-diamines under solution, solvent-free, or solid-phase conditions.
PMID 16872170·J Org Chem·2006
8-other
Mechanism and stereoselectivity of the aza-Wittig reaction between phosphazenes and aldehydes.
PMID 16555840·J Org Chem·2006
8-other
Reaction of 2H-azirine phosphine oxide and -phosphonates with nucleophiles. Stereoselective Synthesis of functionalized aziridines and alpha- and beta-aminophosphorus derivatives.
PMID 16238324·J Org Chem·2005
8-other
Lysosomal targeting of E-cadherin: a unique mechanism for the down-regulation of cell-cell adhesion during epithelial to mesenchymal transitions.
PMID 15601859·Mol Cell Biol·2005
7-preclinical
Preparation of fluoroalkyl imines, amines, enamines, ketones, alpha-amino carbonyls, and alpha-amino acids from primary enamine phosphonates.
PMID 15575755·J Org Chem·2004
8-other
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 251 E HURON ST
CHICAGO, IL 60611 - Phone
- (312) 926-2000
Quick Facts
- NPI
- 1467296574
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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