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PRECIOUS PRINGLE, PHARMD
PHARMD
Pharmacist
NPI: 1902235161Individual
Specialties, Licenses & Credentials
PharmacistPrimary
Pharmacist
Code: 183500000X
14354(SC)25643(NC)
Research & Publications (17)
Anatomy of phobanes. diastereoselective synthesis of the three isomers of n-butylphobane and a comparison of their donor properties.
PMID 19183007·J Am Chem Soc·2009
8-other
Stereoelectronic effects in a homologous series of bidentate cyclic phosphines. A clear correlation of hydroformylation catalyst activity with ring size.
PMID 19081990·Dalton Trans·2009
8-other
Bidentates versus monodentates in asymmetric hydrogenation catalysis: synergic effects on rate and allosteric effects on enantioselectivity.
PMID 18454526·J Am Chem Soc·2008
8-other
A simple entry into nido-C2B10 clusters: HCl promoted cleavage of the C-C bond in ortho-carboranyl diphosphines.
PMID 18322616·Dalton Trans·2008
8-other
Synthesis and reactivity of dichloroboryl complexes of platinum(II).
PMID 17160181·Dalton Trans·2007
8-other
New insights into the mechanism of asymmetric hydrogenation catalysed by monophosphonite-rhodium complexes.
PMID 17377668·Chem Commun (Camb)·2007
8-other
Bulky 4-phosphacyclohexanones: diastereoselective complexations, orthometallations and unprecedented [3.1.1]metallabicycles.
PMID 16967114·Dalton Trans·2006
8-other
Chiral palladium bis(phosphite)PCP-pincer complexes via ligand C-H activation.
PMID 17268657·Chem Commun (Camb)·2006
8-other
Allosteric effects in asymmetric hydrogenation catalysis? Asymmetric induction as a function of the substrate and the backbone flexibility of C1-symmetric diphosphines in rhodium-catalysed hydrogenations.
PMID 17033707·Dalton Trans·2006
8-other
Bulky triarylarsines are effective ligands for palladium catalysed Heck olefination.
PMID 15824787·Dalton Trans·2005
8-other
The electron-poor phosphines P{C6H3(CF3)2-3,5}3 and P(C6F5)3 do not mimic phosphites as ligands for hydroformylation. A comparison of the coordination chemistry of P{C6H3(CF3)2-3,5}3 and P(C6F5)3 and the unexpectedly low hydroformylation activity of their rhodium complexes.
PMID 15782267·Dalton Trans·2005
8-other
Phenylphosphatrioxa-adamantanes: bulky, robust, electron-poor ligands that give very efficient rhodium(I) hydroformylation catalysts.
PMID 15739010·Dalton Trans·2005
8-other
The influence of cigarette smoking on antenatal growth, birth size, and the insulin-like growth factor axis.
PMID 15713720·J Clin Endocrinol Metab·2005
8-other
Special effects of ortho-isopropylphenyl groups. Diastereoisomerism in platinum(II) and palladium(II) complexes of helically chiral PAr3 ligands.
PMID 15702175·Dalton Trans·2005
8-other
Efficient asymmetric hydrogenation with rhodium complexes of C(1)-symmetric 2,5-dimethylphospholane-diphenylphosphines.
PMID 15381999·Dalton Trans·2004
8-other
Sexual dimorphism in the growth hormone and insulin-like growth factor axis at birth.
PMID 12915659·J Clin Endocrinol Metab·2003
3-trial
Factors controlling the relative stabilities of cis- and trans-[PtX2L2] isomers: Chatt and Wilkins--50 years on.
PMID 12585429·Chem Commun (Camb)·2003
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
- 3010 MONROE RD STE 101
CHARLOTTE, NC 28205 - Phone
- (704) 496-9182
Quick Facts
- NPI
- 1902235161
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 2
- Locations
- 1
- Publications
- 17
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