Supplemental material
Cogent Chemistry
Volume 2, 2016 - Issue 1
Related Research Data
Antimicrobial activity of thiazolyl benzenesulfonamide-condensed 2,4-thiazolidinediones derivatives
Source:
Springer Science and Business Media LLC
Structure-activity relationships of a series of 2-amino-4-thiazole-containing renin inhibitors.
Source:
American Chemical Society (ACS)
Lactic acid-mediated tandem one-pot synthesis of 2-aminothiazole derivatives: A rapid, scalable, and sustainable process
Source:
Taylor & Francis
Synthesis, characterization and antimicrobial activity of some new biquinoline derivatives containing a thiazole moiety
Source:
Elsevier BV
Synthesis and structure–activity relationship of N-(3-azabicyclo[3.1.0]hex-6-ylmethyl)-5-(2-pyridinyl)-1,3-thiazol-2-amines derivatives as NPY Y5 antagonists
Source:
Elsevier BV
New Perspectives in Thiazole Chemistry
Source:
Informa UK Limited
Novel series of 3-amino-N-(4-aryl-1,1-dioxothian-4-yl)butanamides as potent and selective dipeptidyl peptidase IV inhibitors
Source:
Elsevier BV
Substituted 4-(Thiazol-5-yl)-2-(phenylamino)pyrimidines Are Highly Active CDK9 Inhibitors: Synthesis, X-ray Crystal Structures, Structure–Activity Relationship, and Anticancer Activities
Source:
American Chemical Society (ACS)
Searching for green solvents
Source:
Royal Society of Chemistry (RSC)
4-(1,2,5,6-Tetrahydro-1-alkyl-3-pyridinyl)-2-thiazolamines: a novel class of compounds with central dopamine agonist properties
Source:
American Chemical Society (ACS)
Design and Synthesis of Human ABCB1 (P-Glycoprotein) Inhibitors by Peptide Coupling of Diverse Chemical Scaffolds on Carboxyl and Amino Termini of (S)-Valine-Derived Thiazole Amino Acid
Source:
American Chemical Society (ACS)
MB06322 (CS-917): A potent and selective inhibitor of fructose 1,6-bisphosphatase for controlling gluconeogenesis in type 2 diabetes
Source:
Proceedings of the National Academy of Sciences
Lactic acid-mediated tandem one-pot synthesis of 2-aminothiazole derivatives: A rapid, scalable, and sustainable process
Source:
Figshare
Efficient Synthesis of 2,4-Disubstituted Thiazoles Under Grinding
Source:
Informa UK Limited
Solution-phase Synthesis of a Combinatorial Library of 3-[4-(Coumarin-3-yl)-1,3-thiazol-2-ylcarbamoyl]propanoic acid Amides
Source:
MDPI AG
Pramipexole Reduces Phosphorylation of α-Synuclein at Serine-129
Source:
Springer Nature
Convenient and simple synthesis of 2-aminothiazoles by the reaction of α-halo ketone carbonyls with ammonium thiocyanate in the presence of N-methylimidazole
Source:
Elsevier BV
Synthesis and Bioactivity of Novel Phenothiazine-Based Thiazole Derivatives
Source:
Informa UK Limited
Lactic acid as an invaluable bio-based solvent for organic reactions
Source:
Royal Society of Chemistry (RSC)
Eco-friendly synthesis of 2-aminothiazoles using Nafion-H as a recyclable catalyst in PEG–water solvent system
Source:
Informa UK Limited
Novel Orally Active Antimalarial Thiazoles
Source:
American Chemical Society (ACS)
Lactic acid mediated tandem one-pot synthesis of 2-aminothiazole derivatives: A rapid, scalable and sustainable process
Source:
Figshare
Catalyst-free efficient synthesis of 2-aminothiazoles in water at ambient temperature
Source:
Elsevier BV
Sodium fluoride as an efficient catalyst for the synthesis of 2,4-disubstituted-1,3-thiazoles and selenazoles at ambient temperature
Source:
Elsevier BV
2-Aminothiazole derivatives as antimycobacterial agents: Synthesis, characterization, in vitro and in silico studies
Source:
Elsevier BV
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