Skip to search formSkip to main contentSkip to account menu

Malonates

Known as: Malonates [Chemical/Ingredient] 
Derivatives of malonic acid (the structural formula CH2(COOH)2), including its salts and esters.
National Institutes of Health

Related topics

Related topics

50 relations

Narrower (44)

2,2-dimethyl-n-benzylmalonamide2-benzylmalonate2-n-butylmalonate2-nitrobenzoylaminomalonate
In Bloodagonistsantagonists & inhibitorsaspects of radiation effects

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
Highly Cited
2011
Highly Cited
2011
MATE2 Mediates Vacuolar Sequestration of Flavonoid Glycosides and Glycoside Malonates in Medicago truncatula[C][W][OA]
This work identifies MATE2, which transports glycosylated flavonoids into the vacuole, showing higher transport efficiency with… 
Highly Cited
2010
Highly Cited
2010
Visible light-mediated intermolecular C-H functionalization of electron-rich heterocycles with malonates.
The photoredox-mediated direct intermolecular C-H functionalization of substituted indoles, pyrroles, and furans with diethyl… 
Review
2009
Review
2009
Asymmetric organocatalysis by chiral Brønsted bases: implications and applications.
Chiral, metal-free Brønsted bases have been demonstrated capable of catalyzing several types of C-C and C-X bond-forming… 
Highly Cited
2008
Highly Cited
2008
The polyphenolic profiles of common bean (Phaseolus vulgaris L.).
Highly Cited
2007
Highly Cited
2007
Detection and quantification of glycosylated flavonoid malonates in celery, Chinese celery, and celery seed by LC-DAD-ESI/MS.
A screening method using LC-DAD-ESI/MS was applied to the analysis of flavonoids in celery, Chinese celery, and celery seeds… 
Highly Cited
2007
Highly Cited
2007
Chiral calcium complexes as brønsted base catalysts for asymmetric addition of α-amino acid derivatives to α,β-unsaturated carbonyl compounds
A novel catalyst system based on complexes of calcium which promote the catalytic asymmetric 1,4-addition reactions and [3+2… 
Highly Cited
2004
Highly Cited
2004
Highly enantioselective conjugate addition of malonate and beta-ketoester to nitroalkenes: asymmetric C-C bond formation with new bifunctional organic catalysts based on cinchona alkaloids.
The development of readily accessible bifunctional chiral catalysts is a desirable yet challenging goal in catalytic asymmetric… 
Highly Cited
2003
Highly Cited
2003
Enantioselective Michael reaction of malonates to nitroolefins catalyzed by bifunctional organocatalysts.
Michael reaction of malonates to nitroolefins with chiral bifunctional organocatalysts, bearing both a thiourea and tertiary… 
Highly Cited
2003
Highly Cited
2003
Transition metal-catalyzed enantioselective ring-opening reactions of oxabicyclic alkenes.
Over the past five years, several metal-catalyzed asymmetric ring-cleaving reactions have been developed that generate ring… 
Highly Cited
2000
Highly Cited
2000
Liquid chromatography-electrospray ionization mass spectrometry study of the flavonoids of the roots of Astragalus mongholicus and A. membranaceus.
By clicking accept or continuing to use the site, you agree to the terms outlined in our Privacy Policy, Terms of Service, and Dataset License