Back to Search
LAUREN DOMINGO, PHARMD
PHARMD
Pharmacist
NPI: 1073253332Individual
Specialties, Licenses & Credentials
PharmacistPrimary
Pharmacist
Code: 183500000X
PH-4754(HI)
Research & Publications (20)
Understanding the mechanism of polar Diels-Alder reactions.
PMID 19675915·Org Biomol Chem·2009
8-other
Toward an understanding of the unexpected regioselective hetero-Diels-Alder reactions of asymmetric tetrazines with electron-rich ethylenes: a DFT study.
PMID 19260699·J Org Chem·2009
8-other
DFT study on the molecular mechanism of the [4 + 2] cycloaddition between thiobenzophenone and arylalkenes via radical cations.
PMID 19385638·J Phys Chem A·2009
8-other
Paleoenvironmental conditions in the Spanish Miocene-Pliocene boundary: isotopic analyses of Hipparion dental enamel.
PMID 19190888·Naturwissenschaften·2009
7-preclinical
DFT study of the molecular mechanism of Lewis acid induced [4 + 3] cycloadditions of 2-alkylacroleins with cyclopentadiene.
PMID 19627132·J Org Chem·2009
8-other
A combined experimental and theoretical study of the polar [3 + 2] cycloaddition of electrophilically activated carbonyl ylides with aldehydes and imines.
PMID 19199802·J Org Chem·2009
8-other
Understanding the participation of quadricyclane as nucleophile in polar [2sigma + 2sigma + 2pi] cycloadditions toward electrophilic pi molecules.
PMID 18942791·J Org Chem·2008
8-other
An understanding of the electrophilic/nucleophilic behavior of electro-deficient 2,3-disubstituted 1,3-butadienes in polar diels-alder reactions. A density functional theory study.
PMID 18370427·J Phys Chem A·2008
8-other
New highly asymmetric Henry reaction catalyzed by Cu(II) and a C(1)-symmetric aminopyridine ligand, and its application to the synthesis of miconazole.
PMID 18384026·Chemistry·2008
8-other
Understanding the reactivity of captodative ethylenes in polar cycloaddition reactions. A theoretical study.
PMID 18484771·J Org Chem·2008
8-other
Understanding reaction mechanisms in organic chemistry from catastrophe theory applied to the electron localization function topology.
PMID 18557601·J Phys Chem A·2008
8-other
Polar [3 + 2] cycloaddition of ketones with electrophilically activated carbonyl ylides. Synthesis of spirocyclic dioxolane indolinones.
PMID 18698474·Org Biomol Chem·2008
8-other
Unusual regioselectivity in the opening of epoxides by carboxylic acid enediolates.
PMID 18596656·Molecules·2008
8-other
Toward an understanding of the acceleration of Diels-Alder reactions by a pseudo-intramolecular process achieved by molecular recognition. A DFT study.
PMID 17465571·J Org Chem·2007
8-other
Triplet reactivity and regio-/stereoselectivity in the macrocyclization of diastereomeric ketoprofen-quencher conjugates via remote hydrogen abstractions.
PMID 17508750·J Am Chem Soc·2007
8-other
New findings on the Diels-Alder reactions. An analysis based on the bonding evolution theory.
PMID 17181354·J Phys Chem A·2006
8-other
Mechanism of triplet photosensitized Diels-Alder Reaction between indoles and cyclohexadienes: theoretical support for an adiabatic pathway.
PMID 16930047·J Org Chem·2006
8-other
1,3-Dipolar cycloadditions of electrophilically activated benzonitrile N-oxides. Polar cycloaddition versus oxime formation.
PMID 17137358·J Org Chem·2006
8-other
Photogeneration and reactivity of 1,n-diphenyl-1,n-azabiradicals.
PMID 16749772·J Org Chem·2006
8-other
Highly diastereoselective one-pot synthesis of spiro[cyclopenta[a]indene-2,2'-indene]diones from 1-indanones and aromatic aldehydes.
PMID 16626127·J Org Chem·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
Via practice · 4 locations total
- Address
- 50 E PUAINAKO ST
HILO, HI 96720 - Phone
- (808) 959-8700
Quick Facts
- NPI
- 1073253332
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 4
- Publications
- 20
Are you this provider?
Claim Your Profile