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MATTHEW JUNG, MD
MD
Internal Medicine Physician
NPI: 1588970115IndividualAccepts Medicare
Specialties, Licenses & Credentials
Internal Medicine PhysicianPrimary
Internal Medicine
Code: 207R00000X
A124125(CA)
Education
OTHER
Class of 2010
Research & Publications (20)
Total synthesis of (+/-)-kellermanoldione: stepwise cycloaddition of a functionalized diene and allenoate.
PMID 19655733·Org Lett·2009
8-other
Synthesis of 2-substituted 7-hydroxybenzofuran-4-carboxylates via addition of silyl enol ethers to o-benzoquinone esters.
PMID 19371072·Org Lett·2009
8-other
Use of 4-cyanocoumarins as dienophiles in a facile synthesis of highly substituted dibenzopyranones.
PMID 19138152·Org Lett·2009
8-other
Improved synthesis of the epoxy isoprostane phospholipid PEIPC and its reactivity with amines.
PMID 18754590·Org Lett·2008
8-other
Preparation of a functionalized tetracyclic intermediate for the synthesis of rhodexin A.
PMID 18642920·Org Lett·2008
8-other
Facile synthesis of cis-2-Alkyl-3-trialkylsilyloxycycloalkanones via the non-aldol aldol rearrangement of 2,3-epoxycycloalkanols.
PMID 18429620·Org Lett·2008
8-other
Anti aldol selectivity in a synthetic approach to the C1-C12 fragment of the tedanolides.
PMID 18067310·Org Lett·2008
7-preclinical
Unprecedented rearrangement of a 4-alkoxy-5-bromoalk-2-en-1-ol to a cyclopentenone via an iso-nazarov cyclization process.
PMID 17910498·J Org Chem·2007
8-other
Synthesis of the C1-C12 fragment of the tedanolides. Aldol-non-aldol aldol approach.
PMID 17676748·Org Lett·2007
7-preclinical
Total synthesis of (+/-)-hedychilactone B: stepwise allenoate diene cycloaddition to prepare trimethyldecalin systems.
PMID 17249787·Org Lett·2007
8-other
Stepwise acid-promoted double-Michael process: an alternative to Diels-Alder cycloadditions for hindered silyloxydiene-dienophile pairs.
PMID 17217308·Org Lett·2007
8-other
Total synthesis of (+/-)-hedychenone: trimethyldecalin terpene systems via stepwise allenoate diene cycloaddition.
PMID 17134290·Org Lett·2006
8-other
Practical syntheses of dyes for difference gel electrophoresis.
PMID 16183291·Bioorg Med Chem·2006
8-other
Synthesis of (2R,3S) 3-amino-4-mercapto-2-butanol, a threonine analogue for covalent inhibition of sortases.
PMID 16169722·Bioorg Med Chem Lett·2005
8-other
Total synthesis of the epoxy isoprostane phospholipids PEIPC and PECPC.
PMID 16119935·Org Lett·2005
8-other
Versatile diastereoselectivity in formal [3,3]-sigmatropic shifts of substituted 1-alkenyl-3-alkylidenecyclobutanols and their silyl ethers.
PMID 16089425·J Am Chem Soc·2005
8-other
Intramolecular Diels-Alder reactions of optically active allenic ketones: chirality transfer in the preparation of substituted oxa-bridged octalones.
PMID 16076181·J Am Chem Soc·2005
8-other
gem-disubstituent effect: theoretical basis and synthetic applications.
PMID 15884788·Chem Rev·2005
6-review
Synthesis of highly substituted cyclohexenes via mixed Lewis acid-catalyzed Diels-Alder reactions of highly substituted dienes and dienophiles.
PMID 15816774·Org Lett·2005
8-other
Synthesis and relative stability of 3,5-diacyl-4,5-dihydro-1H-pyrazoles prepared by dipolar cycloaddition of enones and alpha-diazoketones.
PMID 15609941·J Org Chem·2004
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 · 3 locations total
- Address
- 1031 W 34th St Ste 430
Los Angeles, CA 90089 - Phone
- (213) 821-6500
Quick Facts
- NPI
- 1588970115
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Accepted
- Specialties
- 1
- Locations
- 3
- Years in Practice
- 16
- Publications
- 20
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