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Synthesis and Reactivity of 3H-1,2-dithiole-3-thiones

Molecules (Basel, Switzerland), 2021-06, Vol.26 (12), p.3595

Rakitin, Oleg

2021

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A rare case of brominated small molecule acceptors for high-efficiency organic solar cells

Nature communications, 2023-08, Vol.14 (1), p.4707-4707, Article 4707

2023

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New Cycloadditon Reaction of 2-Chloroprop-2-enethioamides with Dialkyl Acetylenedicarboxylates: Synthesis of Dialkyl 2-[4,5-bis(alkoxycarbonyl)-2-(aryl{alkyl}imino)-3(2H)-thienylidene]-1,3-dithiole-4,5-dicarboxylates

Molecules (Basel, Switzerland), 2022-10, Vol.27 (20), p.6887

2022

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Palladium-Catalyzed Direct (Het)arylation Reactions of Benzo[1,2-d:4,5-d']bis([1,2,3]thiadiazole and 4,8-Dibromobenzo[1,2-d:4,5-d']bis([1,2,3]thiadiazole)

Molecules (Basel, Switzerland), 2023-05, Vol.28 (9), p.3977

2023

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Efficient Synthesis of 4,8-Dibromo Derivative of Strong Electron-Deficient Benzo[1,2-d:4,5-d’]bis([1,2,3]thiadiazole) and Its SNAr and Cross-Coupling Reactions

Molecules (Basel, Switzerland), 2022-11, Vol.27 (21), p.7372

2022

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Benzothiadiazole vs. iso-Benzothiadiazole: Synthesis, Electrochemical and Optical Properties of D–A–D Conjugated Molecules Based on Them

Molecules (Basel, Switzerland), 2021-08, Vol.26 (16), p.4931

2021

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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

Bioorganic & medicinal chemistry letters, 2019-07, Vol.29 (14), p.1765-1768

2019

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Breathing some new life into an old topic: chalcogen-nitrogen π-heterocycles as electron acceptors

Molecules (Basel, Switzerland), 2013-08, Vol.18 (8), p.9850-9900

2013

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Safe Synthesis of 4,7-Dibromo[1,2,5]thiadiazolo[3,4-d]pyridazine and Its SNAr Reactions

Molecules (Basel, Switzerland), 2018-10, Vol.23 (10), p.2576

2018

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[1,2,5]Thiadiazolo[3,4- d ]Pyridazine as an Internal Acceptor in the D-A-π-A Organic Sensitizers for Dye-Sensitized Solar Cells

Molecules (Basel, Switzerland), 2019-04, Vol.24 (8), p.1588

2019

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Benzo[1,2- d :4,5- d ']bis([1,2,3]thiadiazole) and Its Bromo Derivatives: Molecular Structure and Reactivity

International journal of molecular sciences, 2023-05, Vol.24 (10), p.8835

2023

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4-(2,5-Dimethyl-1H-pyrrol-1-yl)-1,2,5-oxadiazol-3-amine

MolBank, 2023-09, Vol.2023 (3), p.M1700

2023

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Novel D-A-π-A1 Type Organic Sensitizers from 4,7-Dibromobenzo[d][1,2,3]thiadiazole and Indoline Donors for Dye-Sensitized Solar Cells

Molecules (Basel, Switzerland), 2022-06, Vol.27 (13), p.4197

2022

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Direct Exchange of Oxygen and Selenium Atoms in the 1,2,5-Oxadiazoles and 1,2,5-Selenadiazoles by Action of Sulfur Monochloride

Molecules (Basel, Switzerland), 2015-08, Vol.20 (8), p.14522-14532

2015

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5-(9-(p-Tolyl)-2,3,4,4a,9,9a-hexahydro-1H-1,4-methanocarbazol-6-yl)thiophene-2-carbaldehyde

MolBank, 2024-03, Vol.2024 (1), p.M1792

2024

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4,4′-Difluoro-[3,3′-bi(1,2,5-oxadiazole)] 2,2′-Dioxide

MolBank, 2023-03, Vol.2023 (1), p.M1596

2023

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4,7-Bis(2,3,3a,8b-tetrahydrocyclopenta[b]indol-4(1H)-yl)-[1,2,5]thiadiazolo[3,4-c]pyridine

MolBank, 2022-09, Vol.2022 (3), p.M1441

2022

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4,4′-([1,2,5]Thiadiazolo[3,4-d]pyridazine-4,7-diyl)bis(N,N-bis(4-methoxyphenyl)aniline)

MolBank, 2022-12, Vol.2022 (4), p.M1479

2022

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Novel D-A-D Fluorescent Dyes Based on 9-(p-Tolyl)-2,3,4,4a,9,9a-hexahydro-1H-carbazole as a Donor Unit for Solution-Processed Organic Light-Emitting-Diodes

Molecules (Basel, Switzerland), 2021-05, Vol.26 (10), p.2872

2021

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5,5′-(Piperazine-1,4-diyl)bis(4-chloro-3H-1,2-dithiol-3-one)

MolBank, 2022-09, Vol.2022 (3), p.M1411

2022

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N-[3-(Chloromethyl)-1,2-benzisoxazol-5-yl]acetamide

MolBank, 2022-06, Vol.2022 (2), p.M1389

2022

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3D molecular network and magnetic ordering, formed by multi-dentate magnetic couplers, bis(benzene)chromium(i) and [1,2,5]thiadiazolo[3,4-c][1,2,5]thiadiazolidyl

Dalton transactions : an international journal of inorganic chemistry, 2018, Vol.47 (29), p.9897-9902

2018

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5,5′-Thiobis(4-chloro-3H-1,2-dithiole-3-thione)

MolBank, 2022-05, Vol.2022 (2), p.M1371

2022

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(E)-4-(2-(7-Bromo-[1,2,5]thiadiazolo[3,4-c]pyridin-4-yl)vinyl)-N,N-diphenylaniline

MolBank, 2022-05, Vol.2022 (2), p.M1368

2022

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Recent Developments in the Synthesis and Applications of 1,2,5-Thia- and Selenadiazoles. A Review

Organic preparations and procedures international, 2014-11, Vol.46 (6), p.475-544

2014

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Synthesis and Reactivity of 3H-1,2-dithiole-3-thiones

A rare case of brominated small molecule acceptors for high-efficiency organic solar cells

New Cycloadditon Reaction of 2-Chloroprop-2-enethioamides with Dialkyl Acetylenedicarboxylates: Synthesis of Dialkyl 2-[4,5-bis(alkoxycarbonyl)-2-(aryl{alkyl}imino)-3(2H)-thienylidene]-1,3-dithiole-4,5-dicarboxylates

Palladium-Catalyzed Direct (Het)arylation Reactions of Benzo[1,2-d:4,5-d']bis([1,2,3]thiadiazole and 4,8-Dibromobenzo[1,2-d:4,5-d']bis([1,2,3]thiadiazole)

Efficient Synthesis of 4,8-Dibromo Derivative of Strong Electron-Deficient Benzo[1,2-d:4,5-d’]bis([1,2,3]thiadiazole) and Its SNAr and Cross-Coupling Reactions

Benzothiadiazole vs. iso-Benzothiadiazole: Synthesis, Electrochemical and Optical Properties of D–A–D Conjugated Molecules Based on Them

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

Breathing some new life into an old topic: chalcogen-nitrogen π-heterocycles as electron acceptors

Safe Synthesis of 4,7-Dibromo[1,2,5]thiadiazolo[3,4-d]pyridazine and Its SNAr Reactions

[1,2,5]Thiadiazolo[3,4- d ]Pyridazine as an Internal Acceptor in the D-A-π-A Organic Sensitizers for Dye-Sensitized Solar Cells

Benzo[1,2- d :4,5- d ']bis([1,2,3]thiadiazole) and Its Bromo Derivatives: Molecular Structure and Reactivity

4-(2,5-Dimethyl-1H-pyrrol-1-yl)-1,2,5-oxadiazol-3-amine

Novel D-A-π-A1 Type Organic Sensitizers from 4,7-Dibromobenzo[d][1,2,3]thiadiazole and Indoline Donors for Dye-Sensitized Solar Cells

Direct Exchange of Oxygen and Selenium Atoms in the 1,2,5-Oxadiazoles and 1,2,5-Selenadiazoles by Action of Sulfur Monochloride

5-(9-(p-Tolyl)-2,3,4,4a,9,9a-hexahydro-1H-1,4-methanocarbazol-6-yl)thiophene-2-carbaldehyde

4,4′-Difluoro-[3,3′-bi(1,2,5-oxadiazole)] 2,2′-Dioxide

4,7-Bis(2,3,3a,8b-tetrahydrocyclopenta[b]indol-4(1H)-yl)-[1,2,5]thiadiazolo[3,4-c]pyridine

4,4′-([1,2,5]Thiadiazolo[3,4-d]pyridazine-4,7-diyl)bis(N,N-bis(4-methoxyphenyl)aniline)

Novel D-A-D Fluorescent Dyes Based on 9-(p-Tolyl)-2,3,4,4a,9,9a-hexahydro-1H-carbazole as a Donor Unit for Solution-Processed Organic Light-Emitting-Diodes

5,5′-(Piperazine-1,4-diyl)bis(4-chloro-3H-1,2-dithiol-3-one)

N-[3-(Chloromethyl)-1,2-benzisoxazol-5-yl]acetamide

3D molecular network and magnetic ordering, formed by multi-dentate magnetic couplers, bis(benzene)chromium(i) and [1,2,5]thiadiazolo[3,4-c][1,2,5]thiadiazolidyl

5,5′-Thiobis(4-chloro-3H-1,2-dithiole-3-thione)

(E)-4-(2-(7-Bromo-[1,2,5]thiadiazolo[3,4-c]pyridin-4-yl)vinyl)-N,N-diphenylaniline

Recent Developments in the Synthesis and Applications of 1,2,5-Thia- and Selenadiazoles. A Review

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