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MADELINE OESTREICH, MD
MD
Family Medicine Physician
NPI: 1508489170IndividualAccepts Medicare
Specialties, Licenses & Credentials
Student in an Organized Health Care Education/Training Program
Student in an Organized Health Care Education/Training Program
Code: 390200000X
Family Medicine PhysicianPrimary
Family Medicine
Code: 207Q00000X
77133-20(WI)
CMS Specialties
PrimaryFAMILY PRACTICE
Education
MEDICAL COLLEGE OF WISCONSIN
Class of 2020
Research & Publications (20)
Strategies for catalytic asymmetric electrophilic alpha halogenation of carbonyl compounds.
PMID 15827954·Angew Chem Int Ed Engl·2005
8-other
"True" chirality transfer from silicon to carbon: asymmetric amplification in a reagent-controlled palladium-catalyzed hydrosilylation.
PMID 15742322·Angew Chem Int Ed Engl·2005
8-other
Catalytic desymmetrizing intramolecular Heck reaction: evidence for an unusual hydroxy-directed migratory insertion.
PMID 15599903·Angew Chem Int Ed Engl·2004
8-other
Facile protocol for the highly regioselective and stereodivergent synthesis of substituted bishomoallylic alcohols from esters.
PMID 15010784·Chem Commun (Camb)·2004
8-other
Potassium tert-butoxide-catalyzed dehydrogenative Si-O coupling: reactivity pattern and mechanism of an underappreciated alcohol protection.
PMID 19153976·Chem Asian J·2009
8-other
Enantiospecific synthesis and allylation of all-carbon-substituted alpha-chiral allylic stannanes.
PMID 19437529·Angew Chem Int Ed Engl·2009
8-other
Palladium(II)-catalyzed conjugate phosphination of electron-deficient acceptors.
PMID 19191507·Org Lett·2009
8-other
Kinetic resolution and desymmetrization by stereoselective silylation of alcohols.
PMID 17987596·Angew Chem Int Ed Engl·2008
8-other
Spin noise spectroscopy in GaAs (110) quantum wells: access to intrinsic spin lifetimes and equilibrium electron dynamics.
PMID 19113364·Phys Rev Lett·2008
8-other
Stereoselective alcohol silylation by dehydrogenative Si-O coupling: scope, limitations, and mechanism of the cu-h-catalyzed non-enzymatic kinetic resolution with silicon-stereogenic silanes.
PMID 19021177·Chemistry·2008
8-other
Conclusive evidence for an S(N)2-Si mechanism in the B(C6F5)3-catalyzed hydrosilylation of carbonyl compounds: implications for the related hydrogenation.
PMID 18613156·Angew Chem Int Ed Engl·2008
8-other
Catalytic asymmetric C-Si bond formation to acyclic alpha,beta-unsaturated acceptors by Rh(I)-catalyzed conjugate silyl transfer using a Si-B linkage.
PMID 18389510·Angew Chem Int Ed Engl·2008
8-other
Kinetic resolution of donor-functionalised tertiary alcohols by Cu-H-catalysed stereoselective silylation using a strained silicon-stereogenic silane.
PMID 18385850·Org Biomol Chem·2008
8-other
Chiral recognition with silicon-stereogenic silanes: remarkable selectivity factors in the kinetic resolution of donor-functionalized alcohols.
PMID 17990256·Angew Chem Int Ed Engl·2007
8-other
Oxygen donor-mediated equilibration of diastereomeric alkene-palladium(II) intermediates in enantioselective desymmetrizing Heck cyclizations.
PMID 17935323·J Am Chem Soc·2007
8-other
Rhodium(i)-catalysed conjugate phosphination of cyclic alpha,beta-unsaturated ketones with silylphosphines as masked phosphinides.
PMID 17668107·Chem Commun (Camb)·2007
8-other
Conformational rigidity of silicon-stereogenic silanes in asymmetric catalysis: A comparative study.
PMID 17288605·Beilstein J Org Chem·2007
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
- 143 S GIBSON ST
MEDFORD, WI 54451 - Phone
- (715) 748-2121
Quick Facts
- NPI
- 1508489170
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Accepted
- Specialties
- 2
- Locations
- 1
- Years in Practice
- 6
- Publications
- 20
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