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JENNIFER PERCY, MD
MD
Obstetrics & Gynecology Physician
NPI: 1154397958IndividualAccepts Medicare
Specialties, Licenses & Credentials
Obstetrics & Gynecology PhysicianPrimary
Obstetrics & Gynecology
Code: 207V00000X
48014(MN)
CMS Specialties
PrimaryOBSTETRICS/GYNECOLOGY
Education
UNIVERSITY OF NORTH DAKOTA SCHOOL OF MEDICINE
Class of 2001
Research & Publications (20)
An appraisal of oxoketene cycloaddition methodology for the synthesis of 2,6-dideoxysugars and fluorinated 2,6-dideoxysugars.
PMID 19343243·Org Biomol Chem·2009
8-other
Sugar nucleotide recognition by Klebsiella pneumoniae UDP-D-galactopyranose mutase: fluorinated substrates, kinetics and equilibria.
PMID 19225684·Org Biomol Chem·2009
8-other
Developing an asymmetric, stereodivergent route to selected 6-deoxy-6-fluoro-hexoses.
PMID 19225683·Org Biomol Chem·2009
8-other
Selected substituent effects on the rate and efficiency of formation of an eight-membered ring by RCM.
PMID 18271601·J Org Chem·2008
8-other
Total syntheses of conformationally locked difluorinated pentopyranose analogues and a pentopyranosyl phosphate mimetic.
PMID 17266373·J Org Chem·2007
8-other
Quantifying the reactivity of a remarkably long-lived difluorinated enol in acidic methanol via solution kinetics and electronic structure calculations.
PMID 17025319·J Org Chem·2006
8-other
Interplay of structure and reactivity in a most unusual furan Diels-Alder reaction.
PMID 17017793·J Am Chem Soc·2006
8-other
Highly-functionalised difluorinated cyclohexane polyols via the Diels-Alder reaction: regiochemical control via the phenylsulfonyl group.
PMID 16132092·Org Biomol Chem·2005
8-other
Towards novel difluorinated sugar mimetics; syntheses and conformational analyses of highly-functionalised difluorinated cyclooctenones.
PMID 16032348·Org Biomol Chem·2005
8-other
A potentially divergent and rapid route to analogues of deoxycyclitols, pentopyranoses, 6-deoxyhexoses, and hexoses.
PMID 15524460·Org Lett·2004
8-other
A stereodivergent asymmetric approach to difluorinated aldonic acids.
PMID 15216363·Chem Commun (Camb)·2004
8-other
A surprising steric effect on a tandem cycloaddition/ring-opening reaction: rapid syntheses of difluorinated analogues of (hydroxymethyl)conduritols.
PMID 15116185·Chem Commun (Camb)·2004
8-other
Unexpectedly selective formation and reactions of epoxycyclooctenones under microwave-mediated conditions.
PMID 15070316·Org Lett·2004
8-other
Synthesis of 4,4-difluoroglycosides using ring-closing metathesis.
PMID 14770232·Org Biomol Chem·2004
8-other
Highly-functionalised difluorinated (hydroxymethyl)conduritol analogues via the Diels-Alder reactions of a difluorinated dienophile.
PMID 14770223·Org Biomol Chem·2004
8-other
Towards conformationally-locked difluorosugar analogues: an unexpected sense of dihydroxylation.
PMID 14740048·Chem Commun (Camb)·2004
8-other
Syntheses of selectively fluorinated cyclodecenones: the first deployment of the neutral oxy-Cope rearrangement in organofluorine chemistry.
PMID 14727631·Org Biomol Chem·2003
8-other
Catalytic asymmetric synthesis of a 1-deoxy-1,1-difluoro-D-xylulose.
PMID 12556186·Org Lett·2003
8-other
Basic and reductive sulfone-directed ring-opening reactions of difluorinated oxa[2.2.1]bicycloheptanes.
PMID 12423102·Org Lett·2002
8-other
Rapid assembly of highly-functionalised difluorinated cyclooctenones via ring-closing metathesis.
PMID 12120378·Chem Commun (Camb)·2002
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
- 606 24TH AVE S, SUITE 700
MINNEAPOLIS, MN 55454 - Phone
- (612) 672-2450
Quick Facts
- NPI
- 1154397958
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Accepted
- Specialties
- 1
- Locations
- 1
- Years in Practice
- 25
- Publications
- 20
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