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Thiazoles
Known as:
Thiazoles [Chemical/Ingredient]
, thiazole
National Institutes of Health
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Related topics
Related topics
50 relations
Narrower (50)
(thiazol-2-yl)hydrazine
2,4,5 trimethylthiazoline
2-amino-6,7-dichlorobenzothiazole
2-benzyl-4-chloromethylthiazole
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Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
Review
2012
Review
2012
Thiazole‐Based Organic Semiconductors for Organic Electronics
Yuze Lin
,
Haijun Fan
,
Yongfang Li
,
X. Zhan
Advances in Materials
2012
Corpus ID: 196973061
Over the past two decades, organic semiconductors have been the subject of intensive academic and commercial interests. Thiazole…
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Review
2008
Review
2008
Cell-penetrating peptides as delivery vehicles for biology and medicine.
Kelly M Stewart
,
Kristin L. Horton
,
S. Kelley
Organic and biomolecular chemistry
2008
Corpus ID: 5185904
Cell-penetrating peptides (CPPs) have found numerous applications in biology and medicine since the first synthetic cell…
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Highly Cited
2007
Highly Cited
2007
Direct arylation of thiazoles on water.
Gemma L Turner
,
J. Morris
,
M. Greaney
Angewandte Chemie
2007
Corpus ID: 5592301
Wetter is better: The direct arylation of thiazoles on water is quicker, cleaner, and higher-yielding than arylation in org…
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Review
2006
Review
2006
Imidazole, oxazole and thiazole alkaloids.
Zhong Jin
Natural product reports (Print)
2006
Corpus ID: 45648667
Covering: July 2004 to June 2005. Previous review: Nat. Prod. Rep., 2005, 22, 196–229Terrestrial and marine microorganisms as…
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Highly Cited
2005
Highly Cited
2005
n-type organic field-effect transistors with very high electron mobility based on thiazole oligomers with trifluoromethylphenyl groups.
S. Ando
,
R. Murakami
,
+4 authors
Y. Yamashita
Journal of the American Chemical Society
2005
Corpus ID: 42413200
Novel thiazole oligomers and thiazole/thiophene co-oligomers with trifluoromethylphenyl groups were developed as n-type…
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Highly Cited
2000
Highly Cited
2000
Thiazole and Thiophene Analogues of Donor−Acceptor Stilbenes: Molecular Hyperpolarizabilities and Structure−Property Relationships
Eric M. Breitung
,
C. Shu
,
R. McMahon
2000
Corpus ID: 97465171
We calculate the first hyperpolarizability (β) of several thiazole and thiophene analogues of donor−acceptor stilbene compounds…
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Highly Cited
1998
Highly Cited
1998
The interactions between the fluorescent dye thiazole orange and DNA.
J. Nygren
,
N. Svanvik
,
M. Kubista
Biopolymers
1998
Corpus ID: 2548656
The interaction of the fluorescent dye thiazole orange (TO) with nucleic acids is characterized. It is found that TO binds with…
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Highly Cited
1991
Highly Cited
1991
ICI D1694, a quinazoline antifolate thymidylate synthase inhibitor that is a potent inhibitor of L1210 tumor cell growth in vitro and in vivo: a new agent for clinical study.
A. Jackman
,
G. A. Taylor
,
+5 authors
L. Hughes
Cancer Research
1991
Corpus ID: 18232892
N-(5-[N-(3,4-dihydro-2-methyl-4-oxoquinazolin-6-ylmethyl)-N- methylamino]-2-thenoyl)-L-glutamic acid (ICI D1694) is a water…
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Highly Cited
1990
Highly Cited
1990
Flow cytometric analysis of thiazole orange uptake by platelets: a diagnostic aid in the evaluation of thrombocytopenic disorders.
J. Kienast
,
G. Schmitz
Blood
1990
Corpus ID: 15015394
Thiazole orange (TO), a fluorescent dye originally synthesized for reticulocyte analysis, is characterized by a large…
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Highly Cited
1986
Highly Cited
1986
Thiazole orange: a new dye for reticulocyte analysis.
L. G. Lee
,
C. H. Chen
,
L. Chiu
Cytometry
1986
Corpus ID: 42891612
The purpose of this study was to find a 488-nm excitable fluorescent dye for reticulocyte analysis by the use of fluorescence…
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