To see the other types of publications on this topic, follow the link: Sulfur heterocycles.

Journal articles on the topic 'Sulfur heterocycles'

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

Select a source type:

Consult the top 50 journal articles for your research on the topic 'Sulfur heterocycles.'

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.

Browse journal articles on a wide variety of disciplines and organise your bibliography correctly.

1

Luna, Isadora Silva, Rayssa Marques Duarte da Cruz, Ryldene Marques Duarte da Cruz, Rodrigo Santos Aquino de Araújo, and Francisco Jaime Bezerra Mendonça-Junior. "1,4-Dithiane-2,5-diol: A Versatile Synthon for the Synthesis of Sulfur-containing Heterocycles." Current Organic Synthesis 15, no. 8 (December 17, 2018): 1026–42. http://dx.doi.org/10.2174/1570179415666180821154551.

Full text
Abstract:
Background: 1,4-Dithiane-2,5-diol (1,4-DTD) is the stable dimer of α-mercapto acetaldehyde. This commercially available ambidentade compound is characterized as having in its chemical structure one group that acts as an electrophile and another that acts as a nucleophile, this permits its use as versatile and efficient synthon in synthetic heterocycle procedures. Objective: The aim of this review is to present synthetic applications of 1,4-DTD in heterocyclic chemistry and their applicability to the synthesis of bioactive compounds. Conclusion: Gewald reactions to obtain C-4 and C-5 unsubstituted 2-amino-thiophene derivatives; sulfa- Michael/Henry and sulfa-Michael/aldol sequences to obtain polysubstituted tetrahydrothiophenes, and other heterocyclic reactions that allow synthesizing several functionalized sulfur-containing heterocycles such as thiazolidines, oxathiazinoles and thiazoles are presented and discussed. The use of such heterocyclics in subsequent reactions allows obtaining various bioactive compounds including the antiretroviral lamivudine which is one of the examples presented in this review.
APA, Harvard, Vancouver, ISO, and other styles
2

Zhu, Yannan, and You Huang. "Organocatalyzed [3+3] Annulations for the Construction of Heterocycles." Synthesis 52, no. 08 (February 5, 2020): 1181–202. http://dx.doi.org/10.1055/s-0039-1690810.

Full text
Abstract:
Six-membered heterocyclic systems are widely distributed in many natural products and pharmaceuticals, and the construction of highly functionalized six-membered heterocyclic compounds is an important topic in modern organic synthesis. Organocatalyzed [3+3] annulations represents an important method for assembling a substantial variety of six-membered cycles that contain one or more heteroatoms. This review describes the development of organocatalyzed [3+3] annulations for the synthesis of six-membered heterocycles, including organocatalysis using secondary amines, tertiary amines, phosphines, chiral phosphoric acids and N-heterocyclic carbenes.1 Introduction2 Secondary Amine Catalyzed [3+3] Annulations2.1 Synthesis of Nitrogen Heterocycles2.2 Synthesis of Oxygen Heterocycles2.3 Synthesis of Sulfur Heterocycles3 Tertiary Amine Catalyzed [3+3] Annulations3.1 Catalysis through Multiple Hydrogen-Bonding Interactions3.2 Catalysis of Tertiary Amines as Lewis Bases4 Phosphine-Catalyzed [3+3] Annulations4.1 Synthesis of Nitrogen Heterocycles4.2 Synthesis of Oxygen Heterocycles4.3 Synthesis of Heterocycles Containing Two or More Heteroatoms5 Chiral Phosphoric Acid Catalyzed [3+3] Annulations5.1 Synthesis of Nitrogen Heterocycles5.2 Synthesis of Heterocycles Containing Two or More Heteroatoms6 N-Heterocyclic Carbene Catalyzed [3+3] Annulations6.1 Synthesis of Nitrogen Heterocycles6.2 Synthesis of Oxygen Heterocycles6.3 Synthesis of Heterocycles Containing Two or More Heteroatoms7 Conclusion and Outlook
APA, Harvard, Vancouver, ISO, and other styles
3

Vasil'eva, T. P., V. M. Bystrova, and O. V. Kil'disheva. "Sulfur heterocycles." Bulletin of the Academy of Sciences of the USSR Division of Chemical Science 37, no. 7 (July 1988): 1448–55. http://dx.doi.org/10.1007/bf00962760.

Full text
APA, Harvard, Vancouver, ISO, and other styles
4

García-Valverde, Maria, and Tomás Torroba. "Sulfur-Nitrogen Heterocycles." Molecules 10, no. 2 (February 28, 2005): 318–20. http://dx.doi.org/10.3390/10020318.

Full text
APA, Harvard, Vancouver, ISO, and other styles
5

Slivka, Mikhailo, and Mikhailo Onysko. "The Use of Electrophilic Cyclization for the Preparation of Condensed Heterocycles." Synthesis 53, no. 19 (May 19, 2021): 3497–512. http://dx.doi.org/10.1055/s-0040-1706036.

Full text
Abstract:
AbstractCondensed heterocycles are well-known for their excellent biological effects and they are undeniably important compounds in organic chemistry. Electrophilic cyclization reactions are widely used for the synthesis of mono-heterocyclic compounds. This review highlights the utility of electrophilic cyclization reactions as an effective generic tool for the synthesis of various condensed heterocycles containing functional groups that are able to undergo further chemical transformations, such as nucleophilic substitution, elimination, re-cyclization, cleavage, etc. This review describes the reactions of unsaturated derivatives of different heterocycles with various electrophilic agents (halogens, arylsulfanyl chlorides, mineral acids) resulting in annulation of an additional partially saturated heterocycle. The electrophilic reaction conditions, plausible mechanisms and the use of such transformations in organic synthesis are also discussed. The review mainly focuses on research published since 2002 in order to establish the current state of the art in this area. 1 Introduction2 Electrophilic Cyclization Pathways Involving a Nitrogen Nucleo­philic Center3 Electrophilic Cyclization Pathways Involving a Chalcogen Nucleophilic Center3.1 Sulfur Centers3.2 Oxygen Centers3.3 Selenium Centers4 Strategies and Mechanisms5 Conclusion
APA, Harvard, Vancouver, ISO, and other styles
6

Randić, Milan, Sonja Nikolić, and Nenad Trinajstić. "Aromaticity in heterocyclic molecules containing divalent sulfur." Collection of Czechoslovak Chemical Communications 53, no. 9 (1988): 2023–54. http://dx.doi.org/10.1135/cccc19882023.

Full text
Abstract:
The conjugated circuits model is applied to heterocycles containing divalent sulfur. A novel parametrization is introduced for 4n + 2 and 4n conjugated circuits containing a single sulfur atom. The relative aromatic stabilities of a number of heterocyclic systems containing divalent sulfur are studied. Comparison is made whenever possible with earlier reported resonance energies of these compounds, obtained by using Huckel MO and SCF π-MO models, and appropriate reference structures. Special attention is given to positional isomers. An explanation of the differences amongst such isomers is given.
APA, Harvard, Vancouver, ISO, and other styles
7

Engelhardt, Udo, and Andre Simon. "Phosphorus-Hydrazine-Sulfur-Heterocycles." Phosphorus, Sulfur, and Silicon and the Related Elements 65, no. 1-4 (February 1992): 65–67. http://dx.doi.org/10.1080/10426509208055319.

Full text
APA, Harvard, Vancouver, ISO, and other styles
8

R. StJ. Foreman, Mark, Josef Novosad, Alexandra M. Z. Slawin, and J. Derek Woollins. "New organophosphorus–sulfur heterocycles." Journal of the Chemical Society, Dalton Transactions, no. 8 (1997): 1347. http://dx.doi.org/10.1039/a608361g.

Full text
APA, Harvard, Vancouver, ISO, and other styles
9

Sharma, Praveen Kumar. "A REVIEW: ANTIMICROBIAL AGENTS BASED ON NITROGEN AND SULFUR CONTAINING HETEROCYCLES." Asian Journal of Pharmaceutical and Clinical Research 10, no. 2 (February 1, 2017): 47. http://dx.doi.org/10.22159/ajpcr.2017.v10i2.15673.

Full text
Abstract:
At present, heterocyclic compounds and their derived forms have become strong reflection in medicinal research field because of their positive pharmacological and biological properties. Heterocycles are prosperous in nature and have expanded additional importance because their structural subunits are established in many natural products such as antibiotics, vitamins, and hormones. Thiazine moieties present in compounds have multiplicity of medicinal activities such as antihypertensive, antitumor, antimicrobial, antibacterial, anticoagulant, antifungal, anticancer, and antiviral. This review article mainly based on thiazines and their derivatives with potential antimicrobial activities that are at this time in advancement.Keywords: Nitrogen, Sulfur heterocycles (thiazines), Antibacterial, Antifungal, Antimicrobial agents.
APA, Harvard, Vancouver, ISO, and other styles
10

Jourdain, F., and J. C. Pommelet. "Synthesis of New Sulfur Heterocycles." Synthetic Communications 27, no. 3 (February 1997): 483–92. http://dx.doi.org/10.1080/00397919708006050.

Full text
APA, Harvard, Vancouver, ISO, and other styles
11

Zwanenburg, B., H. J. F. Philipse, M. M. H. Verstappen, and R. G. Gieling. "Sulfur substituted Small-ring Heterocycles." Phosphorus, Sulfur, and Silicon and the Related Elements 120, no. 1 (January 1, 1997): 453–54. http://dx.doi.org/10.1080/10426509708545594.

Full text
APA, Harvard, Vancouver, ISO, and other styles
12

Sharma, Praveen K., Andleeb Amin, and M. Kumar. "A Review: Medicinally Important Nitrogen Sulphur Containing Heterocycles." Open Medicinal Chemistry Journal 14, no. 1 (September 14, 2020): 49–64. http://dx.doi.org/10.2174/1874104502014010049.

Full text
Abstract:
Nitrogen sulphur containing heterocycles have specific properties due to which they can be used as a potential material in a different type of industries such as medicinal/pharmaceutical, paint, packing and textile, required for various chemical, physical operations and their use as products. Especially dyes, paint, agrochemicals, medicine, etc. make them more significant. In present days, Nitrogen-Sulfur heterocycles are repeatedly attracting the interest of chemists due to their exceptional bioactive behavior. The present study is a review of the work carried out by a chemist in the discovery of new, effective, medicinally important heterocyclic compounds. The present review basically focused on nitrogen-sulfur heterocycles of potential therapeutic interest, especially with thiazole, thiazine, pyrimidine, morpholine and piperazine heterosystems, benzothiazines, pyrazole-benzothiazines, morpholine-benzothiazines, piperazine-benzothiazines and pyrimidine-benzothiazoles, mainly due to their unique structural features, which enable them to exhibit a number of biological and pharmacological activities. Due to a novel mode of action, a broad spectrum of activity, lesser toxicity towards mammalian cells, and suitable profiles towards humans have triggered the use of Nitrogen Sulphur containing heterocycles in designing and synthesizing their derivatives with better properties. The overall objective of the review is to discuss the importance of novel biodynamic structurally diverse heterocycles of potential therapeutic interest: pyrimidine, morpholine, piperazine, pyrozole, benothiazoles, pyrimidobenzothiazoles, 4H-1,4-benzothiazines, pyrazolyl-benzothiazines, morpholinyl-benzothiazines and piperazinylbenzothiazines in order to have access to important commercial molecules for the search of better future.
APA, Harvard, Vancouver, ISO, and other styles
13

García-Valverde, María, and Tomás Torroba. "Heterocyclic Chemistry of Sulfur Chlorides – Fast Ways to Complex Heterocycles." European Journal of Organic Chemistry 2006, no. 4 (February 2006): 849–61. http://dx.doi.org/10.1002/ejoc.200500786.

Full text
APA, Harvard, Vancouver, ISO, and other styles
14

Rakitin, Oleg A. "Synthesis and Reactivity of 3H-1,2-dithiole-3-thiones." Molecules 26, no. 12 (June 11, 2021): 3595. http://dx.doi.org/10.3390/molecules26123595.

Full text
Abstract:
3H-1,2-Dithiole-3-thiones are among the best studied classes of polysulfur-containing heterocycles due to the almost explosive recent interest in these compounds as sources of hydrogen sulfide as an endogenously produced gaseous signaling molecule. This review covers the recent developments in the synthesis of these heterocycles, including both well-known procedures and important novel transformations for building the 1,2-dithiole-3-thione ring. Diverse ring transformations of 3H-1,2-dithiole-3-thiones into various heterocyclic systems through 1,3-dipolar cycloaddition, replacement of one or two sulfur atoms to form carbon- and carbon-nitrogen containing moieties, and other unexpected reactions are considered.
APA, Harvard, Vancouver, ISO, and other styles
15

Majumdar, K. C., and A. K. Pal. "Lewis acid catalyzed Claisen rearrangement: Regioselective synthesis of oxygen, nitrogen, and sulfur heterocycles." Canadian Journal of Chemistry 86, no. 1 (January 1, 2008): 72–78. http://dx.doi.org/10.1139/v07-139.

Full text
Abstract:
Regioselective synthesis of pentacyclic heterocycles containing oxygen, nitrogen, and sulfur has been achieved in good to excellent yields by the sequential Claisen rearrangement of but-2-ynyl ethers and sulfides containing quinolone moiety. The substrates ethers and sulfides were prepared from 1-aryloxy-4-chlorobut-2-ynes with N-alkyl-4-hydroxyquinoline-2(1H)-ones.Key words: regioselectivity, [3,3] sigmatropic rearrangement, nucleophilicity of sulfur, aluminium chloride, heterocycles.
APA, Harvard, Vancouver, ISO, and other styles
16

ENGELHARDT, U., and A. SIMON. "ChemInform Abstract: Phosphorus-Hydrazine-Sulfur-Heterocycles." ChemInform 23, no. 25 (August 21, 2010): no. http://dx.doi.org/10.1002/chin.199225215.

Full text
APA, Harvard, Vancouver, ISO, and other styles
17

Knochel, P., M. Kienle, and A. Unsinn. "Synthesis of Sulfur Heterocycles from Dithiocarbamates." Synfacts 2010, no. 09 (August 23, 2010): 0992. http://dx.doi.org/10.1055/s-0030-1258001.

Full text
APA, Harvard, Vancouver, ISO, and other styles
18

Gabillet, Sandra, Delphine Lecerclé,, Olivier Loreau, Michael Carboni, Sophie Dézard, Jean-Marie Gomis, and Frédéric Taran. "Phosphine-Catalyzed Construction of Sulfur Heterocycles." Organic Letters 9, no. 20 (September 2007): 3925–27. http://dx.doi.org/10.1021/ol701563e.

Full text
APA, Harvard, Vancouver, ISO, and other styles
19

Torroba, Tom?s. "Poly-sulfur-nitrogen heterocycles via sulfur chlorides and nitrogen reagents." Journal für praktische Chemie 341, no. 2 (February 1999): 99–113. http://dx.doi.org/10.1002/(sici)1521-3897(199902)341:2<99::aid-prac99>3.0.co;2-z.

Full text
APA, Harvard, Vancouver, ISO, and other styles
20

Hudson, B. M., E. Nguyen, and D. J. Tantillo. "The influence of intramolecular sulfur–lone pair interactions on small-molecule drug design and receptor binding." Organic & Biomolecular Chemistry 14, no. 16 (2016): 3975–80. http://dx.doi.org/10.1039/c6ob00254d.

Full text
Abstract:
Sulfur–lone pair interactions are important conformational control elements in sulfur-containing heterocycles that abound in pharmaceuticals, natural products, agrochemicals, polymers and other important classes of organic molecules.
APA, Harvard, Vancouver, ISO, and other styles
21

Konstantinova, Lidia S., and Oleg A. Rakitin. "Design of sulfur heterocycles with sulfur monochloride: synthetic possibilities and prospects." Mendeleev Communications 19, no. 2 (March 2009): 55–61. http://dx.doi.org/10.1016/j.mencom.2009.03.001.

Full text
APA, Harvard, Vancouver, ISO, and other styles
22

Bosset, Cyril, Gauthier Lefebvre, Patrick Angibaud, Ian Stansfield, Lieven Meerpoel, Didier Berthelot, Amandine Guérinot, and Janine Cossy. "Iron-Catalyzed Synthesis of Sulfur-Containing Heterocycles." Journal of Organic Chemistry 82, no. 8 (October 13, 2016): 4020–36. http://dx.doi.org/10.1021/acs.joc.6b01827.

Full text
APA, Harvard, Vancouver, ISO, and other styles
23

Willrodt, Imke, and Detlef Geffken. "Sulfur containing heterocycles from α-hydroxy-alkanimidates." European Journal of Pharmaceutical Sciences 4 (September 1996): S111. http://dx.doi.org/10.1016/s0928-0987(97)86334-8.

Full text
APA, Harvard, Vancouver, ISO, and other styles
24

Kaur, Navjeet. "Solid-phase synthesis of sulfur containing heterocycles." Journal of Sulfur Chemistry 39, no. 5 (April 3, 2018): 544–77. http://dx.doi.org/10.1080/17415993.2018.1457673.

Full text
APA, Harvard, Vancouver, ISO, and other styles
25

JOURDAIN, F., and J. C. POMMELET. "ChemInform Abstract: Synthesis of New Sulfur Heterocycles." ChemInform 28, no. 26 (August 4, 2010): no. http://dx.doi.org/10.1002/chin.199726053.

Full text
APA, Harvard, Vancouver, ISO, and other styles
26

Kobayashi, Keiji, Carl Th Pedersen, and Jan Becher. "Sulfur Heterocycles for Organic Conductors and Superconductors." Phosphorus, Sulfur, and Silicon and the Related Elements 43, no. 1-2 (May 1989): 187–208. http://dx.doi.org/10.1080/10426508908040285.

Full text
APA, Harvard, Vancouver, ISO, and other styles
27

Caserio, Marjorie C., and Jhong J. Kim. "Stereoelectronic Effects in Sulfur Heterocycles. Thiosulfonium Ions." Phosphorus and Sulfur and the Related Elements 23, no. 1-3 (June 1985): 169–95. http://dx.doi.org/10.1080/03086648508073385.

Full text
APA, Harvard, Vancouver, ISO, and other styles
28

Muhammad, Mohed Ahmad. "Physical Properties of Cyclestructure." American International Journal of Biology and Life Sciences 1, no. 1 (January 5, 2019): 15–22. http://dx.doi.org/10.46545/aijbls.v1i1.31.

Full text
Abstract:
Azo – cyclic derivatives are a part from a ring that has more than type of atoms. Nitrogen, oxygen and sulfur are often found along with carbon in heterocycles rings. Heterocycles derivatives are common in chemical chemistry, and many have fulfilled important physiological active in plant and animal kingdoms and have an important biological properties, such as, the antibiotic penicillin, sedative phenabarbital, and sugar replacing reagent saccharin, all having heterocycles ring.
APA, Harvard, Vancouver, ISO, and other styles
29

Campos and Berteina-Raboin. "Eucalyptol as a Bio-Based Solvent for Buchwald-Hartwig Reaction on O,S,N-Heterocycles." Catalysts 9, no. 10 (October 10, 2019): 840. http://dx.doi.org/10.3390/catal9100840.

Full text
Abstract:
We report here the use of eucalyptol as a bio-based solvent for the Buchwald–Hartwig reaction on O,S,N-heterocycles. These heterocycles containing oxygen, sulfur and nitrogen were chosen as targets or as starting materials. Once again, eucalyptol demonstrated to be a possible sustainable alternative to common solvents.
APA, Harvard, Vancouver, ISO, and other styles
30

Aly, Ashraf A., Alaa A. Hassan, Maysa M. Makhlouf, and Stefan Bräse. "Chemistry and Biological Activities of 1,2,4-Triazolethiones—Antiviral and Anti-Infective Drugs." Molecules 25, no. 13 (July 3, 2020): 3036. http://dx.doi.org/10.3390/molecules25133036.

Full text
Abstract:
Mercapto-substituted 1,2,4-triazoles are very interesting compounds as they play an important role in chemopreventive and chemotherapeutic effects on cancer. In recent decades, literature has been enriched with sulfur- and nitrogen-containing heterocycles which are used as a basic nucleus of different heterocyclic compounds with various biological applications in medicine and also occupy a huge part of natural products. Therefore, we shed, herein, more light on the synthesis of this interesting class and its application as a biologically active moiety. They might also be suitable as antiviral and anti-infective drugs.
APA, Harvard, Vancouver, ISO, and other styles
31

Woollins, J., Guoxiong Hua, David Cordes, and Alexandra Slawin. "Application of One-Pot Three-Component Condensation Reaction for the Synthesis of New Organophosphorus–Sulfur Macrocycles." Synlett 29, no. 11 (April 19, 2018): 1496–501. http://dx.doi.org/10.1055/s-0037-1609666.

Full text
Abstract:
An efficient approach has been developed for the synthesis of new phosphorus–sulfur heterocycles by a one-pot three-component condensation reaction of a four-membered-ring thionation reagent [Lawesson’s reagent or its ferrocene analogue (2,4-diferrocenyl-1,3,2,4-diathiadiphosphetane 2,4-disulfide)], an alkane- or arenedithiol, and a dihaloalkane at room temperature in the presence of triethylamine. The simple synthesis method with mild conditions (room temperature and normal reactant concentrations) enhances further the application of the multicomponent reaction in the preparation of novel phosphorus–sulfur heterocycles. Six representative X-ray structures confirmed the formation of these macrocycles.
APA, Harvard, Vancouver, ISO, and other styles
32

Fan, Rong, Binbin Liu, Tianyu Zheng, Kun Xu, Chen Tan, Tianlong Zeng, Shuaisong Su, and Jiajing Tan. "An aryne triggered ring-opening fluorination of cyclic thioethers with potassium fluoride." Chemical Communications 54, no. 51 (2018): 7081–84. http://dx.doi.org/10.1039/c8cc03766c.

Full text
APA, Harvard, Vancouver, ISO, and other styles
33

Zheng, Tianyu, Jiajing Tan, Rong Fan, Shuaisong Su, Binbin Liu, Chen Tan, and Kun Xu. "Diverse ring opening of thietanes and other cyclic sulfides: an electrophilic aryne activation approach." Chemical Communications 54, no. 11 (2018): 1303–6. http://dx.doi.org/10.1039/c7cc08553b.

Full text
APA, Harvard, Vancouver, ISO, and other styles
34

Feng, Wei, and Xing-Guo Zhang. "Organophosphine-free copper-catalyzed isothiocyanation of amines with sodium bromodifluoroacetate and sulfur." Chemical Communications 55, no. 8 (2019): 1144–47. http://dx.doi.org/10.1039/c8cc09190k.

Full text
APA, Harvard, Vancouver, ISO, and other styles
35

Torroba, Tomas. "ChemInform Abstract: Poly-Sulfur-Nitrogen Heterocycles via Sulfur Chlorides and Nitrogen Reagents." ChemInform 30, no. 18 (June 16, 2010): no. http://dx.doi.org/10.1002/chin.199918279.

Full text
APA, Harvard, Vancouver, ISO, and other styles
36

Krafft, Christoph, Stefan Brennecke, Frank Ott, Michael Backes, Reiner Salzer, Jörg Grunenberg, Jakob P Ley, Gerhard E Krammer, and Berthold Weber. "High‐Impact Sulfur Compounds: Constitutional and Configurational Assignment of Sulfur‐Containing Heterocycles." Chemistry & Biodiversity 5, no. 6 (June 2008): 1204–12. http://dx.doi.org/10.1002/cbdv.200890097.

Full text
APA, Harvard, Vancouver, ISO, and other styles
37

Martin, Anthony R., Anthony Chartoire, Alexandra M. Z. Slawin, and Steven P. Nolan. "Extending the utility of [Pd(NHC)(cinnamyl)Cl] precatalysts: Direct arylation of heterocycles." Beilstein Journal of Organic Chemistry 8 (September 27, 2012): 1637–43. http://dx.doi.org/10.3762/bjoc.8.187.

Full text
Abstract:
The use of [Pd(NHC)(cinnamyl)Cl] precatalysts in the direct arylation of heterocycles has been investigated. Among four different precatalysts, [Pd(SIPr)(cinnamyl)Cl] proved to be the most efficient promoter of the reaction. The C–H functionalization of sulfur- or nitrogen-containing heterocycles has been achieved at low catalyst loadings. These catalyst charges range from 0.1 to 0.01 mol % palladium.
APA, Harvard, Vancouver, ISO, and other styles
38

Bąchor, Urszula, and Marcin Mączyński. "Selected β2-, β3- and β2,3-Amino Acid Heterocyclic Derivatives and Their Biological Perspective." Molecules 26, no. 2 (January 15, 2021): 438. http://dx.doi.org/10.3390/molecules26020438.

Full text
Abstract:
Heterocyclic moieties, especially five and six-membered rings containing nitrogen, oxygen or sulfur atoms, are broadly distributed in nature. Among them, synthetic and natural alike are pharmacologically active compounds and have always been at the forefront of attention due to their pharmacological properties. Heterocycles can be divided into different groups based on the presence of characteristic structural motifs. The presence of β-amino acid and heterocyclic core in one compound is very interesting; additionally, it very often plays a vital role in their biological activity. Usually, such compounds are not considered to be chemicals containing a β-amino acid motif; however, considering them as this class of compounds may open new routes of their preparation and application as new drug precursors or even drugs. The possibility of their application as nonproteinogenic amino acid residues in peptide or peptide derivatives synthesis to prepare a new class of compounds is also promising. This review highlights the actual state of knowledge about β-amino acid moiety-containing heterocycles presenting antiviral, anti-inflammatory, antibacterial compounds, anaplastic lymphoma kinase (ALK) inhibitors, as well as agonist and antagonists of the receptors.
APA, Harvard, Vancouver, ISO, and other styles
39

Sachar, Anand, Poonam Gupta, Shallu Gupta, and R. L. Sharma. "A novel approach towards the synthesis of tricyclic systems based on pyridine, pyran, thiopyran, azepine, oxepin, thiepin, and pyrimidine rings under different solvent conditions." Canadian Journal of Chemistry 88, no. 5 (May 2010): 478–84. http://dx.doi.org/10.1139/v10-015.

Full text
APA, Harvard, Vancouver, ISO, and other styles
40

Romański, Jarosaw, Grzegorz Mlostoń, and Sylwia Szynkiewicz. "Straightforward Access to New Cage-Functionalized Sulfur Heterocycles." Synthesis, no. 14 (2003): 2259–64. http://dx.doi.org/10.1055/s-2003-41444.

Full text
APA, Harvard, Vancouver, ISO, and other styles
41

Xu, Ping, Bo Yu, Fu Li Li, Xiao Feng Cai, and Cui Qing Ma. "Microbial degradation of sulfur, nitrogen and oxygen heterocycles." Trends in Microbiology 14, no. 9 (September 2006): 398–405. http://dx.doi.org/10.1016/j.tim.2006.07.002.

Full text
APA, Harvard, Vancouver, ISO, and other styles
42

Zayed, Salem E., and Ibrahim A. Hussin. "KETOKETEN gem-DITHIOLS: SYNTHESIS OF SEVERAL SULFUR HETEROCYCLES." Phosphorus, Sulfur, and Silicon and the Related Elements 84, no. 1-4 (November 1, 1993): 191–96. http://dx.doi.org/10.1080/10426509308034331.

Full text
APA, Harvard, Vancouver, ISO, and other styles
43

Fabian, Jürgen, and B. Andes Hess. "λ4σ2-Sulfur Heterocycles. Anab Initioand Density Functional Study." Journal of Organic Chemistry 62, no. 6 (March 1997): 1766–74. http://dx.doi.org/10.1021/jo961776e.

Full text
APA, Harvard, Vancouver, ISO, and other styles
44

Zoller, Uri. "In Pursuit of Stable, Strained Smallring Sulfur Heterocycles." Sulfur reports 20, no. 2 (December 1997): 173–95. http://dx.doi.org/10.1080/01961779708047919.

Full text
APA, Harvard, Vancouver, ISO, and other styles
45

Foreman, Mark R. StJ, Alexandra M. Z. Slawin, and J. Derek Woollins. "Phosphorus–sulfur–nitrogen heterocycles from diferrocenyl dithiadiphosphetane disulfide." Chemical Communications, no. 14 (1997): 1269–70. http://dx.doi.org/10.1039/a702857a.

Full text
APA, Harvard, Vancouver, ISO, and other styles
46

Martins, Andrew, and Mark Lautens. "A Palladium-Catalyzed Approach to Polycyclic Sulfur Heterocycles." Journal of Organic Chemistry 73, no. 22 (November 21, 2008): 8705–10. http://dx.doi.org/10.1021/jo8020105.

Full text
APA, Harvard, Vancouver, ISO, and other styles
47

Nolte, Thies, and Jan T. Andersson. "Capillary electrophoretic separation of polycyclic aromatic sulfur heterocycles." Analytical and Bioanalytical Chemistry 395, no. 6 (August 24, 2009): 1843–52. http://dx.doi.org/10.1007/s00216-009-3034-z.

Full text
APA, Harvard, Vancouver, ISO, and other styles
48

Abdel-Wahab, Bakr F., Saad Shaaban, and Gamal A. El-Hiti. "Synthesis of sulfur-containing heterocycles via ring enlargement." Molecular Diversity 22, no. 2 (January 31, 2018): 517–42. http://dx.doi.org/10.1007/s11030-017-9810-3.

Full text
APA, Harvard, Vancouver, ISO, and other styles
49

Majumdar, Krishna C., and Anwesha Bandyopadhyay. "Synthesis of Sulfur Heterocycles by Thio- Claisen Rearrangement." Monatshefte f�r Chemie / Chemical Monthly 135, no. 5 (May 1, 2004): 581–87. http://dx.doi.org/10.1007/s00706-003-0109-y.

Full text
APA, Harvard, Vancouver, ISO, and other styles
50

Dočekal, Vojtěch, Bedřich Formánek, Ivana Císařová, and Jan Veselý. "Correction: A formal [4 + 2] cycloaddition of sulfur-containing alkylidene heterocycles with allenic compounds." Organic Chemistry Frontiers 6, no. 22 (2019): 3810. http://dx.doi.org/10.1039/c9qo90096a.

Full text
APA, Harvard, Vancouver, ISO, and other styles
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!

To the bibliography