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2-styryl-4-ethoxymethylene-5-oxazolone

Known as: 5(4H)-Oxazolone, 4-(ethoxymethylene)-2-(2-phenylethenyl)-, (S-(R*,R*))-, styryl ox, styryloxazolone 
National Institutes of Health

Papers overview

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Highly Cited
2017
Highly Cited
2017
Inter- or intramolecular hydroamination reactions are a paradigmatic example of modern sustainable organic chemistry, as they are… 
Review
2013
Review
2013
Since the first report and due to its handiness and wide scope, the Suzuki-Miyaura (SM) cross coupling reaction has become a… 
Highly Cited
2012
Highly Cited
2012
Indoles are a common heterocyclic motif embedded in a large number of bioactive natural products and pharmaceuticals.[1] As such… 
Highly Cited
2012
Highly Cited
2012
Organofluorine compounds have found application in a wide variety of fields. They occur, for example, in pharmaceuticals… 
Review
2011
Review
2011
Highly Cited
2007
Highly Cited
2007
A convenient and clean “on water”-mediated synthesis of benzothiazoles/benzothiazolines is reported. Aromatic, heteroaromatic… 
Highly Cited
2007
Highly Cited
2007
Several 3-[5-(4-substituted)phenyl-1,3,4-oxadiazole-2-yl]-2-styryl quinazoline-4(3H)-one were synthesized and screened for… 
Review
2006
Review
2006
Nature is an inexhaustible source of natural compounds with interesting biological activities. In general, natural products are… 
Highly Cited
2005
Highly Cited
2005
Membrane potential measurements using voltage-sensitive dyes (VSDs) have made important contributions to our understanding of… 
Highly Cited
1995
Highly Cited
1995
  • T. Vida, S. Emr
  • The Journal of cell biology
  • 1995
  • Corpus ID: 15495893
We have used a lipophilic styryl dye, N-(3-triethylammoniumpropyl)-4- (p-diethylaminophenyl-hexatrienyl) pyridinium dibromide (FM…