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MIRIAN ORGAN, MD
MD
Obstetrics & Gynecology Physician
NPI: 1255318564Individual
Specialties, Licenses & Credentials
Obstetrics & Gynecology PhysicianPrimary
Obstetrics & Gynecology
Code: 207V00000X
49987-020(WI)
Research & Publications (20)
Density functional theory investigation of the alkyl-alkyl Negishi cross-coupling reaction catalyzed by N-heterocyclic carbene (NHC)-Pd complexes.
PMID 19288489·Chemistry·2009
8-other
Pd-PEPPSI-IPent: an active, sterically demanding cross-coupling catalyst and its application in the synthesis of tetra-ortho-substituted biaryls.
PMID 19226587·Angew Chem Int Ed Engl·2009
8-other
Assessing synthetic strategies: total syntheses of (+/-)-neodolabellane-type diterpenoids.
PMID 18666272·Chemistry·2008
8-other
High yielding alkylations of unactivated sp3 and sp2 centres with alkyl-9-BBN reagents using an NHC-based catalyst: Pd-PEPPSI-IPrf.
PMID 18478707·Chem Commun (Camb)·2008
8-other
Diels-Alder cycloadditions by microwave-assisted, continuous flow organic synthesis (MACOS): the role of metal films in the flow tube.
PMID 18253521·Chem Commun (Camb)·2008
8-other
Pd-catalyzed aryl amination mediated by well defined, N-heterocyclic carbene (NHC)-Pd precatalysts, PEPPSI.
PMID 18224651·Chemistry·2008
8-other
Pd PEPPSI-IPr-mediated reactions in metal-coated capillaries under MACOS: the synthesis of indoles by sequential aryl amination/Heck coupling.
PMID 18080264·Chemistry·2008
8-other
Gold-film-catalysed hydrosilylation of alkynes by microwave-assisted, continuous-flow organic synthesis (MACOS).
PMID 18816566·Chemistry·2008
8-other
Palladium complexes of N-heterocyclic carbenes as catalysts for cross-coupling reactions--a synthetic chemist's perspective.
PMID 17410611·Angew Chem Int Ed Engl·2007
6-review
A 2.13 A structure of E. coli dihydrofolate reductase bound to a novel competitive inhibitor reveals a new binding surface involving the M20 loop region.
PMID 17125251·J Med Chem·2006
8-other
Easily prepared air- and moisture-stable Pd-NHC (NHC=N-heterocyclic carbene) complexes: a reliable, user-friendly, highly active palladium precatalyst for the Suzuki-Miyaura reaction.
PMID 16568494·Chemistry·2006
8-other
A user-friendly, all-purpose Pd-NHC (NHC=N-heterocyclic carbene) precatalyst for the negishi reaction: a step towards a universal cross-coupling catalyst.
PMID 16568493·Chemistry·2006
8-other
Catalysis in capillaries by Pd thin films using microwave-assisted continuous-flow organic synthesis (MACOS).
PMID 16548038·Angew Chem Int Ed Engl·2006
8-other
The first Negishi cross-coupling reaction of two alkyl centers utilizing a Pd-N-heterocyclic carbene (NHC) catalyst.
PMID 16092880·Org Lett·2005
8-other
Room-temperature Negishi cross-coupling of unactivated alkyl bromides with alkyl organozinc reagents utilizing a Pd/N-heterocyclic carbene catalyst.
PMID 16209599·J Org Chem·2005
8-other
A microcapillary system for simultaneous, parallel microwave-assisted synthesis.
PMID 16163759·Chemistry·2005
8-other
A microreactor for microwave-assisted capillary (continuous flow) organic synthesis.
PMID 15926844·J Am Chem Soc·2005
8-other
Electronic nature of N-heterocyclic carbene ligands: effect on the Suzuki reaction.
PMID 15876037·Org Lett·2005
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
- 2555 N MARTIN LUTHER KING DR
MILWAUKEE, WI 53212 - Phone
- (414) 372-8080
Quick Facts
- NPI
- 1255318564
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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