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Carbamates:PrThr:Pt:Gast fld:Ord:Screen
Known as:
Carbamates:Présence-Seuil:Temps ponctuel:Liquide gastrique:Ordinal:Dépistage
, Carbamates [Seuil] Liquide gastrique ; Qualitatif ; Dépistage
, carbamatos:concentración arbitraria:punto en el tiempo:líquidos/contenidos gástricos:ordinal:tamizaje
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2 relations
Carbamates
Toxicology screen, general (procedure)
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
Highly Cited
2014
Highly Cited
2014
Novel Sulphamides and Sulphonamides Incorporating the Tetralin Scaffold as Carbonic Anhydrase and Acetylcholine Esterase Inhibitors
Akın Akıncıoğlu
,
M. Topal
,
I. Gülçin
,
S. Göksu
Archiv der Pharmazie
2014
Corpus ID: 32793682
Reactions of amino, aminomethyl tetralins and benzyl alcohol with chlorosulphonyl isocyanate (CSI) afforded sulphamoyl carbamates…
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Highly Cited
2014
Highly Cited
2014
Carbonic anhydrase inhibitory properties of novel benzylsulfamides using molecular modeling and experimental studies.
S. Göksu
,
A. Naderi
,
+5 authors
R. E. Salmas
Bioorganic chemistry (Print)
2014
Corpus ID: 36431929
Highly Cited
2013
Highly Cited
2013
Retention or inversion in stereospecific nickel-catalyzed cross-coupling of benzylic carbamates with arylboronic esters: control of absolute stereochemistry with an achiral catalyst.
Michael R Harris
,
Luke E. Hanna
,
M. A. Greene
,
C. Moore
,
E. Jarvo
Journal of the American Chemical Society
2013
Corpus ID: 21073292
Stereospecific coupling of benzylic carbamates and pivalates with aryl- and heteroarylboronic esters has been developed. The…
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Highly Cited
2013
Highly Cited
2013
Evaluation of NHS carbamates as a potent and selective class of endocannabinoid hydrolase inhibitors.
M. Niphakis
,
A. Cognetta
,
+6 authors
B. Cravatt
ACS Chemical Neuroscience
2013
Corpus ID: 23952790
Monoacylglycerol lipase (MAGL) is a principal metabolic enzyme responsible for hydrolyzing the endogenous cannabinoid…
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Highly Cited
2013
Highly Cited
2013
Synthesis and carbonic anhydrase inhibitory properties of sulfamides structurally related to dopamine.
Kadir Aksu
,
Meryem Nar
,
+5 authors
C. Supuran
Bioorganic & Medicinal Chemistry
2013
Corpus ID: 7510983
Highly Cited
2011
Highly Cited
2011
Suzuki-Miyaura cross-coupling of aryl carbamates and sulfamates: experimental and computational studies.
K. Quasdorf
,
Aurora Antoft-Finch
,
+7 authors
N. Garg
Journal of the American Chemical Society
2011
Corpus ID: 28083789
The first Suzuki-Miyaura cross-coupling reactions of the synthetically versatile aryl O-carbamate and O-sulfamate groups are…
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Highly Cited
2011
Highly Cited
2011
Rapid nickel-catalyzed Suzuki-Miyaura cross-couplings of aryl carbamates and sulfamates utilizing microwave heating.
M. Baghbanzadeh
,
Christian Pilger
,
C. Kappe
Journal of Organic Chemistry
2011
Corpus ID: 20997513
High-speed and scalable nickel-catalyzed cross-coupling of arylboronic acids with aryl carbamates and sulfamates is achieved by…
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Highly Cited
2009
Highly Cited
2009
Suzuki-Miyaura coupling of aryl carbamates, carbonates, and sulfamates.
K. Quasdorf
,
M. Riener
,
K. V. Petrova
,
N. Garg
Journal of the American Chemical Society
2009
Corpus ID: 207146887
The first Suzuki-Miyaura cross-couplings of carbamates, carbonates, and sulfamates is described. The method provides a powerful…
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Highly Cited
2006
Highly Cited
2006
Gold(I)-catalyzed intramolecular hydroamination of alkenyl carbamates.
Xiaoqing Han
,
R. Widenhoefer
Angewandte Chemie
2006
Corpus ID: 41376835
Highly Cited
1984
Highly Cited
1984
Protection against both lethal and behavioral effects of soman.
L. Harris
,
J. McDonough
,
D. Stitcher
,
W. J. Lennox
Drug and chemical toxicology (New York, N.Y. )
1984
Corpus ID: 7509317
This work developed two drug mixtures which alone had no effect on performance of a criterion behavior but when given as a…
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