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EDGARDO REYES, MD
MD
Family Medicine Physician
NPI: 1881715480Individual
Specialties, Licenses & Credentials
Research & Publications (20)
Enantioselective organocatalytic domino oxa-Michael/aldol/hemiacetalization: synthesis of polysubstituted furofuranes containing four stereocenters.
PMID 19557777·Angew Chem Int Ed Engl·2009
8-other
Meteorological and agricultural effects on airborne Alternaria and Cladosporium spores and clinical aspects in Valladolid (Spain).
PMID 19572478·Ann Agric Environ Med·2009
8-other
Uranium series disequilibria in ground waters from a fractured bedrock aquifer (Morungaba Granitoids--Southern Brazil): implications to the hydrochemical behavior of dissolved U and Ra.
PMID 18514535·Appl Radiat Isot·2008
8-other
Effects of combined cholinergic-purinergic block upon cat carotid body chemoreceptors in vitro.
PMID 16959549·Respir Physiol Neurobiol·2007
7-preclinical
Carotid body chemosensory activity and ventilatory chemoreflexes in cats persist after combined cholinergic-purinergic block.
PMID 16956797·Respir Physiol Neurobiol·2007
7-preclinical
(S,S)-(+)-Pseudoephedrine as chiral auxiliary in asymmetric conjugate addition and tandem conjugate addition/alpha-alkylation reactions.
PMID 16995684·J Org Chem·2006
8-other
Are there interactions between acetylcholine- and ATP-induced responses at the level of a visceral sensory ganglion?
PMID 16824493·Brain Res·2006
4-observational
Organocatalytic asymmetric michael addition of aldehydes to beta-nitroacroleine dimethyl acetal.
PMID 17165948·Org Lett·2006
8-other
Tandem asymmetric conjugate addition/alpha-alkylation using (S,S)-(+)-pseudoephedrine as chiral auxiliary.
PMID 16737307·Org Lett·2006
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
- 816 FEATHERSTONE RD
ROCKFORD, IL 61107 - Phone
- (815) 227-0081
Quick Facts
- NPI
- 1881715480
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 2
- Locations
- 1
- Publications
- 20
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