2-Aminothiazole (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "2-Aminothiazole" in English language version.

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7doi.org

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4nih.gov

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1semanticscholar.org

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doi.org

Dahlmanns, Simone M.; Müller-Gärtner, Hans-Wilhelm (2000). "Thyrotherapeutic Agents". Ullmann's Encyclopedia of Industrial Chemistry. doi:10.1002/14356007.a27_039. ISBN 9783527303854.
Erlenmeyer, H.; Herzfeld, L.; Prijs, B. (1955). "Zur Synthese von 2-Amino-thiazolderivaten". Helvetica Chimica Acta. 38 (5): 1291–1294. doi:10.1002/hlca.19550380529.
J. R. Byers; J. B. Dickey (1939). "2-Amino-4-methylthiazole". Organic Syntheses. 19: 10. doi:10.15227/orgsyn.019.0010.
Gómez, Antonio Bermejo; Ahlsten, Nanna; Platero-Prats, Ana E.; Martín-Matutejournal=Organic Syntheses, Belén (2014). "Synthesis of 4,5-Disubstituted 2-Aminothiazoles from α,β-Unsaturated Ketones: Preparation of 5-Benzyl-4-methyl-2-aminothiazolium Hydrochloride Salt". Organic Syntheses. 91: 185–200. doi:10.15227/orgsyn.091.0185.
Alajarín, M.; Cabrera, J.; Pastor, A.; Sánchez-Andrada, P.; Bautista, D. (2006). "On the [2+2] Cycloaddition of 2-Aminothiazoles and Dimethyl Acetylenedicarboxylate. Experimental and Computational Evidence of a Thermal Disrotatory Ring Opening of Fused Cyclobutenes". J. Org. Chem. 71 (14): 5328–5339. doi:10.1021/jo060664c. PMID 16808523.
Das, Debasis; Sikdar, Papiya; Bairagi, Moumita (2016). "Recent Developments of 2-Aminothiazoles in Medicinal Chemistry". European Journal of Medicinal Chemistry. 109: 89–98. doi:10.1016/j.ejmech.2015.12.022. PMID 26771245.
Wan, Yichao; Long, Jiabing; Gao, Han; Tang, Zilong (2021). "2-Aminothiazole: A privileged scaffold for the discovery of anti-cancer agents". European Journal of Medicinal Chemistry. 210. doi:10.1016/j.ejmech.2020.112953. PMID 33148490. S2CID 226258989.

nih.gov

pubmed.ncbi.nlm.nih.gov

Alajarín, M.; Cabrera, J.; Pastor, A.; Sánchez-Andrada, P.; Bautista, D. (2006). "On the [2+2] Cycloaddition of 2-Aminothiazoles and Dimethyl Acetylenedicarboxylate. Experimental and Computational Evidence of a Thermal Disrotatory Ring Opening of Fused Cyclobutenes". J. Org. Chem. 71 (14): 5328–5339. doi:10.1021/jo060664c. PMID 16808523.
Das, Debasis; Sikdar, Papiya; Bairagi, Moumita (2016). "Recent Developments of 2-Aminothiazoles in Medicinal Chemistry". European Journal of Medicinal Chemistry. 109: 89–98. doi:10.1016/j.ejmech.2015.12.022. PMID 26771245.
Wan, Yichao; Long, Jiabing; Gao, Han; Tang, Zilong (2021). "2-Aminothiazole: A privileged scaffold for the discovery of anti-cancer agents". European Journal of Medicinal Chemistry. 210. doi:10.1016/j.ejmech.2020.112953. PMID 33148490. S2CID 226258989.

pubchem.ncbi.nlm.nih.gov

"2-Aminothiazole". pubchem.ncbi.nlm.nih.gov. Retrieved 12 December 2022.

semanticscholar.org

api.semanticscholar.org

Wan, Yichao; Long, Jiabing; Gao, Han; Tang, Zilong (2021). "2-Aminothiazole: A privileged scaffold for the discovery of anti-cancer agents". European Journal of Medicinal Chemistry. 210. doi:10.1016/j.ejmech.2020.112953. PMID 33148490. S2CID 226258989.