Log in

Relevant bibliographies by topics / 5-thiadiazine dioxides

Contents

Journal articles

Academic literature on the topic '5-thiadiazine dioxides'

Author: Grafiati

Published: 5 June 2025

Last updated: 1 August 2025

Create a spot-on reference in APA, MLA, Chicago, Harvard, and other styles

Select a source type:

Consult the lists of relevant articles, books, theses, conference reports, and other scholarly sources on the topic '5-thiadiazine dioxides.'

Next to every source in the list of references, there is an 'Add to bibliography' button. Press on it, and we will generate automatically the bibliographic reference to the chosen work in the citation style you need: APA, MLA, Harvard, Chicago, Vancouver, etc.

You can also download the full text of the academic publication as pdf and read online its abstract whenever available in the metadata.

Journal articles on the topic "5-thiadiazine dioxides"

1

Innes, Dylan, Michael V. Perkins, Andris J. Liepa, and Craig L. Francis. "N,N-Dialkyl-N′-Chlorosulfonyl Chloroformamidines in Heterocyclic Synthesis. Part XIV. Synthesis and Reactivity of the New Benzo[4,5]imidazo[1,2-b][1,2,6]thiadiazine Ring System." Australian Journal of Chemistry 71, no. 1 (2018): 58. http://dx.doi.org/10.1071/ch17255.

Full text

Abstract:

N,N-Dialkyl-N′-chlorosulfonyl chloroformamidines 1 underwent regioselective reactions with the 1,3-NCC bis-nucleophilic 1H-benzimidazole-2-acetonitriles 4 and related compounds to produce benzo[4,5]imidazo[1,2-b][1,2,6]thiadiazine dioxides 6, 9, 12, and 14, representatives of a new ring system. Reaction of dichlorides 1 with trifluoroacetyl derivative 16 afforded benzo[4,5]imidazo[1,2-c]pyrimidines 19 and 20. An N-acyl and some N-alkyl derivatives of benzimidazo-thiadiazines 6 were prepared to demonstrate the potential of this new ring system as a novel scaffold for synthetic and medicinal che

APA, Harvard, Vancouver, ISO, and other styles

2

Di Santo, R., R. Costi, M. Artico, et al. "1,2,5-Benzothiadiazepine and Pyrrolo[2,1-d]-[1,2,5]Benzothiadiazepine Derivatives with Specific Anti-Human Immunodeficiency Virus Type 1 Activity." Antiviral Chemistry and Chemotherapy 9, no. 2 (1998): 127–37. http://dx.doi.org/10.1177/095632029800900204.

Full text

Abstract:

We synthesized and tested as novel inhibitors of human immunodeficiency virus type 1 (HIV-1) bi- and tricyclic thiadiazine ring homologues of 7-chloro-2-ethyl-2 H-1,2,4-benzothiadiazin-3-(4 H)-one 1,1-dioxide, which is a compound endowed with anti-HIV-1 activity at low micromolar concentrations. Benzothiadiazepine derivatives were obtained by alkylation of 8-chloro-2,3-dihydro-3-methyl-1,2,5-benzothiadiazepin-4(5 H)-one 1,1-dioxide, which was obtained by intramolecular cyclization of 2-(2-amino-5-chloro-benzenesulphonamido) propanoic acid. Pyrrolobenzothiadiazepines were synthesized from N-sub

APA, Harvard, Vancouver, ISO, and other styles

3

LEE, C. H., Y. H. LEE, W. S. CHOI, and B. Y. CHUNG. "ChemInform Abstract: Synthesis of 4-Carbethoxy-5-aryl-5,6-dihydro-2H-1,2,6-thiadiazine 1,1- Dioxides." ChemInform 24, no. 16 (2010): no. http://dx.doi.org/10.1002/chin.199316216.

Full text

APA, Harvard, Vancouver, ISO, and other styles

4

Innes, Dylan, Michael V. Perkins, Andris J. Liepa, and Craig L. Francis. "N,N-Dialkyl-N′-Chlorosulfonyl Chloroformamidines in Heterocyclic Synthesis. Part XV. Some Unexpected Reactions with Anilines." Australian Journal of Chemistry 71, no. 8 (2018): 610. http://dx.doi.org/10.1071/ch18252.

Full text

Abstract:

N,N-Dimethyl-N′-chlorosulfonyl chloroformamidine 1a underwent reactions with various anilines. In addition to the benzo[e][1,2,4]thiadiazine dioxides 8, from 1,3-NCC bis-nucleophilic substitution and bis-anilino adducts 9, some unexpected products were formed, particularly when sterically hindered or electron-poor anilines were used. In these cases, products such as the [1,3,2,4,6]dithiatriazine 1,1,3,3-tetraoxides 17 and, on occasion, N,N,5-trimethyl-4-(arylimino)-4,5-dihydro-[1,3,5]triazin-2-amines 14 were produced in significant yields. Reaction of dichloride 1a with 3-bromoaniline afforded

APA, Harvard, Vancouver, ISO, and other styles

5

Susanta, K. Borthakur, Boruah Paran, and N. Goswami Birendra. "[4+2] Cycloaddition reaction: Synthesis and antifungal activities of 2-substituted 1,2,4-triazolo[3,2-c][1,3,5]thiadiazine-3,3-dioxides." Journal of Indian Chemical Society Vol. 90, Jul 2013 (2013): 1005–8. https://doi.org/10.5281/zenodo.5774794.

Full text

Abstract:

Department of Chemistry, Arya Vidyapeeth College, P.O. Gopinath Nagar, Guwahati-781 016, Assam, India <em>E-mail</em> : skbthakur@yahoo.co.in Medicinal Aromatic and Economic Plant Division, Formerly of Synthetic Organic Chemistry Division, North East Institute of Science and Technology, Jorhat-785 006, Assam, India <em>Manuscript received online 06 August 2012, revised 09 August 2012, accepted 16 August 2012</em> 3-Benzylidineamino-1,2,4-triazole undergoes [4+2] cycloaddition reaction with sulfene resulting in good yield of [1,2,4]-triazolo[3,2-<em>c</em>][1,3,5]-thiadiazine-3,3-dioxide deriva

APA, Harvard, Vancouver, ISO, and other styles

6

Goya, Pilar, and Ana Martinez. "N-Glucosyl-5-amino-4-carbamoyl- and 4-Ethoxycarbonylimidazoles as Potential Precursors of 4-Oxoimdazo[4,5-c]-1,2,6-thiadiazine 2,2-Dioxides." HETEROCYCLES 24, no. 12 (1986): 3451. http://dx.doi.org/10.3987/r-1986-12-3451.

Full text

APA, Harvard, Vancouver, ISO, and other styles

7

Ochoa, Carmen, Angela Herrero, Juan Antonio P�z, Mart地 Mart地ez-Ripoll, Concepci溶 Foces-Foces, and F四ix Hernadez Cano. "A New Route for the Synthesis of 6-Substitutes Imidazo[4-5,c]-1,2,6-thiadiazine 2,2-Dioxides: Nmr Study and Crystal Structure of a Complex with Dimethylformamide." HETEROCYCLES 26, no. 12 (1987): 3123. http://dx.doi.org/10.3987/r-1987-12-3123.

Full text

APA, Harvard, Vancouver, ISO, and other styles

8

Gong, Tang, Liu та Liu. "Synthesis and Evaluation of Novel 2H-Benzo[e]-[1,2,4]thiadiazine 1,1-Dioxide Derivatives as PI3Kδ Inhibitors". Molecules 24, № 23 (2019): 4299. http://dx.doi.org/10.3390/molecules24234299.

Full text

Abstract:

In previous work, we applied the rotation-limiting strategy and introduced a substituent at the 3-position of the pyrazolo [3,4-d]pyrimidin-4-amine as the affinity element to interact with the deeper hydrophobic pocket, discovered a series of novel quinazolinones as potent PI3Kδ inhibitors. Among them, the indole derivative 3 is one of the most selective PI3Kδ inhibitors and the 3,4-dimethoxyphenyl derivative 4 is a potent and selective dual PI3Kδ/γ inhibitor. In this study, we replaced the carbonyl group in the quinazolinone core with a sulfonyl group, designed a series of novel 2H-benzo[e][1

APA, Harvard, Vancouver, ISO, and other styles

9

Clerici, Francesca, Franco Galletti, Donato Pocar, and Pietro Roversi. "Isothiazoles. Part VI. Cycloaddition of azides to isothiazole dioxides: Synthesis of thiadiazabicyclo[3.1.0]hexene derivatives and their thermal rearrangement to thiazete dioxides, 1,2,6-thiadiazine dioxides and pyrazoles." Tetrahedron 52, no. 20 (1996): 7183–200. http://dx.doi.org/10.1016/0040-4020(96)00336-5.

Full text

APA, Harvard, Vancouver, ISO, and other styles

10

Gobis, Katarzyna, Henryk Foks, Jarosłw Sławiński, Ewa Augustynowicz-Kopeć, and Agnieszka Napiórkowska. "Synthesis and biological activity of novel 3-heteroaryl-2H-pyrido[4,3-e][1,2,4]thiadiazine and 3-heteroaryl-2H-benzo[e][1,2,4]thiadiazine 1,1-dioxides." Monatshefte für Chemie - Chemical Monthly 144, no. 8 (2013): 1197–203. http://dx.doi.org/10.1007/s00706-013-0988-5.

Full text

APA, Harvard, Vancouver, ISO, and other styles

More sources

We offer discounts on all premium plans for authors whose works are included in thematic literature selections. Contact us to get a unique promo code!