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Items: 4

1.

Synthesis and comparison of substituted 1,2,3-dithiazole and 1,2,3-thiaselenazole as inhibitors of the feline immunodeficiency virus (FIV) nucleocapsid protein as a model for HIV infection.

Asquith CRM, Meili T, Laitinen T, Baranovsky IV, Konstantinova LS, Poso A, Rakitin OA, Hofmann-Lehmann R.

Bioorg Med Chem Lett. 2019 Jul 15;29(14):1765-1768. doi: 10.1016/j.bmcl.2019.05.016. Epub 2019 May 9.

PMID:
31101470
2.

The Conversion of 5,5'-Bi(1,2,3-dithiazolylidenes) into Isothiazolo[5,4-d]isothiazoles.

Konstantinova LS, Baranovsky IV, Strunyasheva VV, Kalogirou AS, Popov VV, Lyssenko KA, Koutentis PA, Rakitin OA.

Molecules. 2018 May 24;23(6). pii: E1257. doi: 10.3390/molecules23061257.

3.

Fused 1,2,3-Thiaselenazoles Synthesized from 1,2,3-Dithiazoles through Selective Chalcogen Exchange.

Konstantinova LS, Baranovsky IV, Pritchina EA, Mikhailov MS, Bagryanskaya IY, Semenov NA, Irtegova IG, Salnikov GE, Lyssenko KA, Gritsan NP, Zibarev AV, Rakitin OA.

Chemistry. 2017 Dec 1;23(67):17037-17047. doi: 10.1002/chem.201703182. Epub 2017 Nov 8.

PMID:
28885741
4.

Fused 1,2,3-Dithiazoles: Convenient Synthesis, Structural Characterization, and Electrochemical Properties.

Konstantinova LS, Baranovsky IV, Irtegova IG, Bagryanskaya IY, Shundrin LA, Zibarev AV, Rakitin OA.

Molecules. 2016 May 6;21(5). pii: E596. doi: 10.3390/molecules21050596.

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