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VIVEK NAIR, M.D.
M.D.
Internal Medicine Physician
NPI: 1801824065IndividualAccepts Medicare
Specialties, Licenses & Credentials
Internal Medicine PhysicianPrimary
Internal Medicine
Code: 207R00000X
0101240116(VA)
CMS Specialties
PrimaryINTERNAL MEDICINE
Education
OTHER
Class of 2002
Research & Publications (20)
Strategies in infrapopliteal intervention: improving outcomes in challenging patients.
PMID 19281520·J Interv Cardiol·2009
8-other
Nucleophilic heterocyclic carbene catalyzed annulation of enals to chalcones in methanol: a stereoselective synthesis of highly functionalized cyclopentanes.
PMID 19459619·Org Lett·2009
8-other
Recent advances in carbon-carbon bond-forming reactions involving homoenolates generated by NHC catalysis.
PMID 19020682·Chem Soc Rev·2008
8-other
Stereoselective synthesis of spirocyclopentanones via N-heterocyclic carbene-catalyzed reactions of enals and dienones.
PMID 18478711·Chem Commun (Camb)·2008
8-other
An efficient synthesis of indolo[3,2-a]carbazoles via the novel acid catalyzed reaction of indoles and diaryl-1,2-diones.
PMID 18452007·Org Biomol Chem·2008
8-other
Carbon-nitrogen bond-forming reactions of dialkyl azodicarboxylate: a promising synthetic strategy.
PMID 18412188·Chem Asian J·2008
6-review
A novel reaction of the "Huisgen zwitterion" with chalcones and dienones: an efficient strategy for the synthesis of pyrazoline and pyrazolopyridazine derivatives.
PMID 17286329·Angew Chem Int Ed Engl·2007
8-other
An N-heterocyclic carbene-catalyzed [8 + 3] annulation of tropone and enals via homoenolate.
PMID 17081031·J Org Chem·2006
8-other
Engaging zwitterions in carbon-carbon and carbon-nitrogen bond-forming reactions: A promising synthetic strategy.
PMID 16906748·Acc Chem Res·2006
8-other
N-heterocyclic carbene-catalyzed reaction of chalcones and enals via homoenolate: an efficient synthesis of 1,3,4-trisubstituted cyclopentenes.
PMID 16819860·J Am Chem Soc·2006
8-other
Novel synthesis of highly functionalized pyrazolines and pyrazoles by triphenylphosphine-mediated reaction of dialkyl azodicarboxylate with allenic esters.
PMID 16706489·Org Lett·2006
8-other
Reaction of dimethoxycarbene-DMAD zwitterion with 1,2-diones and anhydrides: a novel synthesis of highly substituted dihydrofurans and spirodihydrofurans.
PMID 16526779·J Org Chem·2006
8-other
N-heterocyclic carbene catalyzed reaction of enals and 1,2-dicarbonyl compounds: stereoselective synthesis of spiro gamma-butyrolactones.
PMID 16435871·Org Lett·2006
8-other
Pyridine-catalyzed addition of diaryl-1,2-diones to dimethyl butynedioate leading to the formation of 1,2-diaroyl dimethyl maleates via an unprecedented rearrangement.
PMID 15760171·Org Lett·2005
8-other
Practical synthesis of triaryl- and triheteroarylmethanes by reaction of aldehydes and activated arenes promoted by gold(III) chloride.
PMID 16354084·Org Lett·2005
8-other
Reaction of Huisgen zwitterion with 1,2-benzoquinones and isatins: expeditious synthesis of dihydro-1,2,3-benzoxadiazoles and spirooxadiazolines.
PMID 16268522·Org Lett·2005
8-other
Engaging the pyridine-DMAD zwitterion in a novel strategy for the selective synthesis of highly substituted benzene and cyclopentenedione derivatives.
PMID 16209495·Org Lett·2005
8-other
Two unprecedented multicomponent reactions involving N-heterocyclic carbenes, activated acetylenes, and aldehydes.
PMID 15932182·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
- 4660 KENMORE AVE, SUITE 710
ALEXANDRIA, VA 22304 - Phone
- (703) 370-9002
Quick Facts
- NPI
- 1801824065
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Accepted
- Specialties
- 1
- Locations
- 1
- Years in Practice
- 24
- Publications
- 20
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