Log in

Relevant bibliographies by topics / Acyl isothiocyanates / Journal articles

To see the other types of publications on this topic, follow the link: Acyl isothiocyanates.

Journal articles on the topic 'Acyl isothiocyanates'

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 top 50 journal articles for your research on the topic 'Acyl isothiocyanates.'

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

Kutschy, Peter, Milan Dzurilla, Ladislav Kniežo, et al. "Reactions of 3-butine-2-methyl-2-ol with isothiocyanates." Collection of Czechoslovak Chemical Communications 51, no. 5 (1986): 1119–26. http://dx.doi.org/10.1135/cccc19861119.

Full text

Abstract:

3-Butine-2-methyl-2-ol reacts with isothiocyanates in the presence of sodium hydride in dimethylformamide to give various products depending on structure of the isothiocyanate residue. Isothiocyanates with the NCS group bound to sp2 carbon atom (phenyl, 4-bromophenyl, and styryl isothiocyanates) give the respective 1,3-oxazolidine derivatives. If the NCS group is bound to an sp3-hybridized carbon atom (ethyl and benzyl isothiocyanates), derivatives of 1,3-oxathiolane are formed. Acyl isothiocyanates (benzoyl and 3-phenylpropenoyl isothiocyanates) give products of substitution of the NCS group,

APA, Harvard, Vancouver, ISO, and other styles

2

Kniežo, Ladislav, and Juraj Bernát. "A Convenient Synthesis of Tertiary Isothiocyanates and Acyl Isothiocyanates Using Phosphoryl Isothiocyanate." Synthetic Communications 20, no. 4 (1990): 509–13. http://dx.doi.org/10.1080/00397919008244898.

Full text

APA, Harvard, Vancouver, ISO, and other styles

3

Kholodniak, Olena, and Sergiy Kovalenko. "Substituted acyl thioureas and acyl thiosemicarbazides: synthesis and biological activity (minireview)." ScienceRise: Pharmaceutical Science, no. 2(36) (April 29, 2022): 56–71. http://dx.doi.org/10.15587/2519-4852.2022.255738.

Full text

Abstract:

Acyl isothiocyanates and their functional derivatives (acyl thioureas and acyl thiosemicarbazides) are an important group of organic compounds that are widely used in the synthesis of heterocycles and in chemistry as catalysts, ligands, colorimetric hemosensors, etc. In recent years, there has been an increased interest towards this class of compounds as promising biologically active compounds, especially since the latest advances in medicinal chemistry for them are not sufficiently studied. The aim. To summarize and systematize information for the last 10 years on methods of synthesis a

APA, Harvard, Vancouver, ISO, and other styles

4

Olena, Kholodniak, and Kovalenko Sergiy. "Substituted acyl thioureas and acyl thiosemicarbazides: synthesis and biological activity (minireview)." ScienceRise: Pharmaceutical Science, no. 2(36) (April 29, 2022): 56–71. https://doi.org/10.15587/2519-4852.2022.255738.

Full text

Abstract:

Acyl isothiocyanates and their functional derivatives (acyl thioureas and acyl thiosemicarbazides) are an important group of organic compounds that are widely used in the synthesis of heterocycles and in chemistry as catalysts, ligands, colorimetric hemosensors, etc. In recent years, there has been an increased interest towards this class of compounds as promising biologically active compounds, especially since the latest advances in medicinal chemistry for them are not sufficiently studied. <strong>The aim. </strong>To summarize and systematize information for the last 10 years on method

APA, Harvard, Vancouver, ISO, and other styles

5

Kulkarni, Pravin S., Amol U. Khandebharad, Swapnil R. Sarda, and Brijmohan R. Agrawal. "Synthesis and Docking Studies of Novel Bis(2-(Substituted(methyl)amino)-4-phenylthiazol-5-yl)methanone." Asian Journal of Chemistry 34, no. 11 (2022): 3015–20. http://dx.doi.org/10.14233/ajchem.2022.24030.

Full text

Abstract:

A new series of novel synthesis of bis(2-(substituted(methyl)amino)-4-phenylthiazol-5-yl)methanone (PVS 1-9) is reported. The carbonyl isothiocyanate (3) was synthesized by a para-cleavage of C–Cl bond of benzoyl chloride (1) with ammonium thiocyanate (2). The presence of carbonyl group in acyl isothiocyanates enhance the reactivity of acyl isothiocyanates upon reaction with substituted secondary amine (4) give n-alkylated adduct (5), which upon the reaction with dichloro acetone give target compound 7. Substituted derivatives as inhibitors against lungs, breast and EJFR assist cancer based on

APA, Harvard, Vancouver, ISO, and other styles

6

L'Abbé, Gerrit, Agna Francis, Wim Dehaen, and Joris Bosman. "Reactions of acyl isothiocyanates with diphenyldiazomethane." Bulletin des Sociétés Chimiques Belges 105, no. 5 (2010): 253–58. http://dx.doi.org/10.1002/bscb.19961050507.

Full text

APA, Harvard, Vancouver, ISO, and other styles

7

Palsuledesai, Charuta C., Siva Murru, Santosh K. Sahoo, and Bhisma K. Patel. "Acyl-isothiocyanates as Efficient Thiocyanate Transfer Reagents." Organic Letters 11, no. 15 (2009): 3382–85. http://dx.doi.org/10.1021/ol901561j.

Full text

APA, Harvard, Vancouver, ISO, and other styles

8

L'abbé, Gerrit, Mitsuo Komatsu, Catherina Martens, et al. "Heterocycles from Acyl Isothiocyanates and Alkyl Azides." Bulletin des Sociétés Chimiques Belges 88, no. 4 (2010): 245–51. http://dx.doi.org/10.1002/bscb.19790880408.

Full text

APA, Harvard, Vancouver, ISO, and other styles

9

Bedane, Kibrom G., and Girija S. Singh. "Reactivity and diverse synthetic applications of acyl isothiocyanates." Arkivoc 2015, no. 6 (2015): 206–45. http://dx.doi.org/10.3998/ark.5550190.p009.052.

Full text

APA, Harvard, Vancouver, ISO, and other styles

10

L'ABBE, G., A. FRANCIS, W. DEHAEN, and J. BOSMAN. "ChemInform Abstract: Reactions of Acyl Isothiocyanates with Diphenyldiazomethane." ChemInform 27, no. 34 (2010): no. http://dx.doi.org/10.1002/chin.199634076.

Full text

APA, Harvard, Vancouver, ISO, and other styles

11

A., S. Singha, S. Kaith B., S. Chauhan G., Thakur A., C. Rao G., and N. Misra B. "Reactions of isothiocyanates with N-acyl-O-alkylhydroxylamines and benzyloxyamine." Journal of Indian Chemical Society Vol. 76, Jun 1999 (1999): 317–18. https://doi.org/10.5281/zenodo.5852420.

Full text

Abstract:

Department of Applied Sciences, Regional Engineering College, Hamirpur-177 005, India Department of Chemistry, Himachal Pradesh University, Summer Hill, Shimla-171 005, India <em>Manuscript received 21 April 1997, revised 5 February 1999, accepted 24 February 1999</em> The reactions of α-naphthyl isothiocyanate, allyl isothiocyanate and <em>n</em>-propyl isothiocyanate with some <em>N</em>-acyl-<em>O</em>-alkylhydroxylamine and benzyloxyamine have been investigated.

APA, Harvard, Vancouver, ISO, and other styles

12

Mahadevaiah, Raghavendra, Lalithamba Haraluru Shankraiah та Latha Haraluru Kamalamma Eshwaraiah. "Combustion Synthesis of Nano Fe2O3 and its Utilization as a Catalyst for the Synthesis of Nα-Protected Acyl Thioureas and Study of Anti-bacterial Activities". Acta Chimica Slovenica 69, № 1 (2022): 116–24. https://doi.org/10.17344/acsi.2021.7055.

Full text

Abstract:

A simple and eco-friendly nano Fe2O3 heterogeneous catalytic system is described for the synthesis of acyl thiourea derivatives from corresponding in situ generated acyl isothiocyanates and amino acid esters in acetone obtained in good yields. The structures of synthesized acyl thioureas were confimed by 1H NMR, 13C NMR, mass, and FTIR analysis. Fe2O3 NPs has been prepared via a solution combustion route using ascorbic acid as the reducing agent and ferric nitrate as the source of iron. The prepared nano material has been characterized by XRD, SEM, UV-Visible, and FTIR analysis. More prominent

APA, Harvard, Vancouver, ISO, and other styles

13

Vovk, M. V., N. G. Chubaruk, and A. V. Bol'but. "New Route of Reaction between Acyl Isothiocyanates and Cyclic -Diketones." Russian Journal of Organic Chemistry 40, no. 2 (2004): 280–81. http://dx.doi.org/10.1023/b:rujo.0000034955.48174.8f.

Full text

APA, Harvard, Vancouver, ISO, and other styles

14

Bedane, Kibrom G., and Girija S. Singh. "ChemInform Abstract: Reactivity and Diverse Synthetic Applications of Acyl Isothiocyanates." ChemInform 46, no. 36 (2015): no. http://dx.doi.org/10.1002/chin.201536291.

Full text

APA, Harvard, Vancouver, ISO, and other styles

15

Vafina, G. F., and A. I. Poptsov. "2-Allyl- and 2-Benzylmaleopimarimide Acyl Isothiocyanates: Synthesis of Triazoles." Russian Journal of General Chemistry 94, no. 3 (2024): 508–13. http://dx.doi.org/10.1134/s1070363224030022.

Full text

APA, Harvard, Vancouver, ISO, and other styles

16

Vafina, G. F., and A. I. Poptsov. "Synthesis and spectral characteristics of hydrazinocarbonothioyl derivatives of maleopimaric acid." Журнал общей химии 93, no. 8 (2023): 1178–89. http://dx.doi.org/10.31857/s0044460x23080048.

Full text

Abstract:

Reaction of acyl isothiocyanates of 2-allyl- and 2-benzylmaleopimarimides with 3-carboxy- and 2,4-dinitrophenylhydrazines and hydrazides of some aromatic acids (benzoic, 4-hydroxy- and 4-methoxybenzoic, nicotinic, isonicotinic) furnished linear hydrazinocarbonothioyl derivatives of these maleopimarimides in high yields. Structure of the synthesized compounds was determined by 1H,13C, 1H-13C HSQC, 1H-13C HMBC, COSY, NOESY, and 1H-15N HMBC NMR spectroscopy methods.

APA, Harvard, Vancouver, ISO, and other styles

17

Koshelev, Vladimir N., Ludmila V. Ivanova, Rahman T. Kh Alasadi, and Olga V. Primerova. "SYNTHESIS OF NOVEL 4-R-1,2,4-TRIAZOLIN-5-THIONES CONTAINING SPACE-HINDERED FRAGMENT OF PHENOL." IZVESTIYA VYSSHIKH UCHEBNYKH ZAVEDENIY KHIMIYA KHIMICHESKAYA TEKHNOLOGIYA 60, no. 3 (2017): 42. http://dx.doi.org/10.6060/tcct.2017603.5473.

Full text

Abstract:

Using of additives inhibiting free radical processes is necessary at production of the lubricating oils. In given article such kind target compounds were obtained from the number of new 1-acyl-4-R-thiosemicarbazides which were synthesized on the base of 3- (4-hydroxy-3,5-di-tert-butyl) propanoic acid hydrazide. The starting hydrazide was prepared from commercially available methyl ester (methylox) by refluxing in ethanol with a slight excess of hydrazine hydrate for 8 h. The best yields of the 1-acyl-4-R-isothiocyanates were achieved by refluxing equimolar amounts of isothiocyanates and hydraz

APA, Harvard, Vancouver, ISO, and other styles

18

Ficeri, Vlastimír, Peter Kutschy, Milan Dzurilla, and Ján Imrich. "[3,3]- Versus [1,3]-Sigmatropic Rearrangement of O-Substituted Allyl N-Acylmonothiocarbamates." Collection of Czechoslovak Chemical Communications 59, no. 12 (1994): 2650–62. http://dx.doi.org/10.1135/cccc19942650.

Full text

Abstract:

Substituted allylic alcohols (2-buten-1-ol, 1-buten-3-ol, cinnamyl alcohol and 3-methyl-2-buten-1-ol) react with acyl isothiocyanates (4-chlorobenzoyl, 2,6-difluorobenzoyl, 3-phenylpropenoyl, 2-thienocarbonyl, 3-chloro-2-thienocarbonyl and 3-chloro-2-benzo[b]thienocarbonyl isothiocyanate) with the formation of highly reactive O-substituted allyl N-acylmonothiocarbamates, which either spontaneously or by heating in boiling benzene undergo [3,3]-sigmatropic rearrangement to S-substituted allyl N-acylmonothiocarbamates. The structure of S-esters with isomerized allylic group affords the unequivoc

APA, Harvard, Vancouver, ISO, and other styles

19

Singha, A. S., B. S. Kaith, G. S. Chauhan, A. Thakur, G. C. Rao, and B. N. Misra. "ChemInform Abstract: Reactions of Isothiocyanates with N-Acyl-O-alkylhydroxylamines and Benzyloxyamine." ChemInform 31, no. 19 (2010): no. http://dx.doi.org/10.1002/chin.200019038.

Full text

APA, Harvard, Vancouver, ISO, and other styles

20

Vafina, G. F., and A. I. Poptsov. "Acyl Isothiocyanates of 2-Allyl- and 2-Benzylmaleopimarimide: Synthesis of 1,3,4-Thiadiazoles." Russian Journal of General Chemistry 94, no. 3 (2024): 514–21. http://dx.doi.org/10.1134/s1070363224030034.

Full text

APA, Harvard, Vancouver, ISO, and other styles

21

Koshelev, Vladimir N., Olga V. Primerova, Stepan V. Vorobyev, and Natalya A. Vakhromova. "Synthesis and Antioxidant Activity of 2-Amino-5-R-1,3,4-Oxadiazoles with Hindered Phenol Fragments." Chemistry Proceedings 3, no. 1 (2020): 69. http://dx.doi.org/10.3390/ecsoc-24-08407.

Full text

Abstract:

Compounds with hindered phenolic moiety are known to be effective inhibitors of oxidative processes in different materials; moreover, a number of phenols show a wide spectrum of biological activity. At the same time, five-membered heterocycles exhibit unique properties, including antioxidant activity. One of the ways to create new effective antioxidants with a set of useful properties is to combine hindered phenol and a heterocyclic fragment in one molecule. In this work, new 1-acyl-4-R-thiosemicarbazides were obtained during a reaction between 3-(4-hydroxy-3,5-di-tert-butylphenyl)propanoic ac

APA, Harvard, Vancouver, ISO, and other styles

22

L'abbé, Gerrit, Ingrid Sannen, and Wim Dehaen. "Synthesis of fused dihydro-1,2,4-thiadiazolimines from cyano-substituted azides and acyl isothiocyanates." J. Chem. Soc., Perkin Trans. 1, no. 1 (1993): 27–29. http://dx.doi.org/10.1039/p19930000027.

Full text

APA, Harvard, Vancouver, ISO, and other styles

23

Hansell, David P., and Robert F. Hudson. "The reaction of oximes and phenols with acyl isothiocyanates; an example of regioselectivity." Journal of the Chemical Society, Chemical Communications, no. 20 (1985): 1405. http://dx.doi.org/10.1039/c39850001405.

Full text

APA, Harvard, Vancouver, ISO, and other styles

24

Nishida, Shouko, Masaya Shibano, Hiroshi Kamitakahara, and Toshiyuki Takano. "Basic study for acyl chitosan isothiocyanates synthesis by model experiments using glucosamine derivatives." International Journal of Biological Macromolecules 132 (July 2019): 17–23. http://dx.doi.org/10.1016/j.ijbiomac.2019.03.114.

Full text

APA, Harvard, Vancouver, ISO, and other styles

25

Muzychka, L. V., O. B. Smolii, and B. S. Drach. "Syntheses of Functionalized Pyrimidines from the Products of Addition of Triphenylphosphoranylideneacetonitrile to Acyl Isothiocyanates." Russian Journal of General Chemistry 74, no. 7 (2004): 1115–21. http://dx.doi.org/10.1023/b:rugc.0000045875.40116.eb.

Full text

APA, Harvard, Vancouver, ISO, and other styles

26

Shibano, Masaya, Shouko Nishida, Yasuko Saito, Hiroshi Kamitakahara, and Toshiyuki Takano. "Facile synthesis of acyl chitosan isothiocyanates and their application to porphyrin-appended chitosan derivative." Carbohydrate Polymers 113 (November 2014): 279–85. http://dx.doi.org/10.1016/j.carbpol.2014.05.099.

Full text

APA, Harvard, Vancouver, ISO, and other styles

27

L'ABBE, G., I. SANNEN, and W. DEHAEN. "ChemInform Abstract: Synthesis of Fused Dihydro-1,2,4-thiadiazolimines from Cyanosubstituted Azides and Acyl Isothiocyanates." ChemInform 24, no. 16 (2010): no. http://dx.doi.org/10.1002/chin.199316196.

Full text

APA, Harvard, Vancouver, ISO, and other styles

28

Khaje-Kolaki, Aslan, and Babak Mokhtari. "Phosphine-free Direct Conversion of Carboxylic Acids into Acyl Isothiocyanates Using Various Electrophilic Halogenation Reagents." Letters in Organic Chemistry 15, no. 9 (2018): 805–8. http://dx.doi.org/10.2174/1570178615666180330155606.

Full text

APA, Harvard, Vancouver, ISO, and other styles

29

Entezari, Najmeh, Batool Akhlaghinia, and Hamed Rouhi-Saadabad. "Direct and Facile Synthesis of Acyl Isothiocyanates from Carboxylic Acids Using Trichloroisocyanuric Acid/Triphenylphosphine System." Croatica Chemica Acta 87, no. 3 (2014): 201–6. http://dx.doi.org/10.5562/cca2381.

Full text

APA, Harvard, Vancouver, ISO, and other styles

30

Kondratyuk, K. M., E. I. Lukashuk, A. V. Golovchenko, and V. S. Brovarets. "Reaction of diethyl 5-hydrazino-2-(4-methylphenyl)-1,3-oxazol-4-ylphosphonate with acyl isothiocyanates." Russian Journal of General Chemistry 82, no. 11 (2012): 1781–86. http://dx.doi.org/10.1134/s1070363212110060.

Full text

APA, Harvard, Vancouver, ISO, and other styles

31

L'abbé, Gerrit, Agna Francis, Wim Dehaen, and Suzanne Toppet. "Reactions of acyl isothiocyanates with diphenyldiazomethane: a route to oxazole derivatives and thietan-3-imines." J. Chem. Soc., Chem. Commun., no. 1 (1995): 67–68. http://dx.doi.org/10.1039/c39950000067.

Full text

APA, Harvard, Vancouver, ISO, and other styles

32

Abdelazeem, Ahmed H., Yasser M. A. Mohamed, Ahmed M. Gouda, Hany A. Omar, and Majed M. Al Robaian. "Novel Thymohydroquinone Derivatives as Potential Anticancer Agents: Design, Synthesis, and Biological Screening." Australian Journal of Chemistry 69, no. 11 (2016): 1277. http://dx.doi.org/10.1071/ch16102.

Full text

Abstract:

The safety and efficacy of naturally occurring anticancer agents and their derivatives such as thymoquinone (TQ) and thymohydroquinone (THQ) have gained a rapidly growing interest. In an attempt to develop novel anticancer agents with superior activity, TQ was allowed to react with hydrazine hydrate, producing hydrazino thymohydroquinone 3. This new intermediate was subsequently reacted with various isocyanates, isothiocyanates, and acyl halides, affording three series of semicarbazone, semithiocarbazone, and acyl hydrazone derivatives, respectively. Subsequently, the anticancer activity of al

APA, Harvard, Vancouver, ISO, and other styles

33

Abdelazeem, Ahmed H., Yasser M. A. Mohamed, Ahmed M. Gouda, Hany A. Omar, and Majed M. Al Robaian. "Corrigendum to: Novel Thymohydroquinone Derivatives as Potential Anticancer Agents: Design, Synthesis, and Biological Screening." Australian Journal of Chemistry 70, no. 6 (2017): 755. http://dx.doi.org/10.1071/ch16102_co.

Full text

Abstract:

The safety and efficacy of naturally occurring anticancer agents and their derivatives such as thymoquinone (TQ) and thymohydroquinone (THQ) have gained a rapidly growing interest. In an attempt to develop novel anticancer agents with superior activity, TQ was allowed to react with hydrazine hydrate, producing hydrazino thymohydroquinone 3. This new intermediate was subsequently reacted with various isocyanates, isothiocyanates, and acyl halides, affording three series of semicarbazone, semithiocarbazone, and acyl hydrazone derivatives, respectively. Subsequently, the anticancer activity of al

APA, Harvard, Vancouver, ISO, and other styles

34

Assy, M. G. "REACTION OF ACYL ISOTHIOCYANATES WITH NUCLEOPHILES: A CONVENIENT SYNTHESIS OF 1,3-OXAZINE, PYRIMIDINETHIONE AND THIAZOLE DERIVATIVES." Phosphorus, Sulfur, and Silicon and the Related Elements 108, no. 1-4 (1996): 15–20. http://dx.doi.org/10.1080/10426509608029633.

Full text

APA, Harvard, Vancouver, ISO, and other styles

35

Wiberg, Kenneth B., Yi-gui Wang, Scott J. Miller, Angela L. A. Puchlopek, William F. Bailey, and Justin D. Fair. "Disparate Behavior of Carbonyl and Thiocarbonyl Compounds: Acyl Chlorides vs Thiocarbonyl Chlorides and Isocyanates vs Isothiocyanates." Journal of Organic Chemistry 74, no. 10 (2009): 3659–64. http://dx.doi.org/10.1021/jo9004316.

Full text

APA, Harvard, Vancouver, ISO, and other styles

36

L'abbé, Gerrit, Agna Francis, and Wim Dehaen. "Reactions of acyl isothiocyanates with 9-diazofluorene: a route to macromolecules having pairs of orthogonal fluorene groups." J. Chem. Soc., Perkin Trans. 1, no. 12 (1996): 1349–51. http://dx.doi.org/10.1039/p19960001349.

Full text

APA, Harvard, Vancouver, ISO, and other styles

37

L'ABBE, G., A. FRANCIS, W. DEHAEN, and S. TOPPET. "ChemInform Abstract: Reactions of Acyl Isothiocyanates with Diphenyldiazomethane: A Route to Oxazole Derivatives and Thietan-3-imines." ChemInform 26, no. 23 (2010): no. http://dx.doi.org/10.1002/chin.199523133.

Full text

APA, Harvard, Vancouver, ISO, and other styles

38

Entezari, Najmeh, Batool Akhlaghinia, and Hamed Rouhi-Saadabad. "ChemInform Abstract: Direct and Facile Synthesis of Acyl Isothiocyanates from Carboxylic Acids Using Trichloroisocyanuric Acid/Triphenylphosphine System." ChemInform 46, no. 19 (2015): no. http://dx.doi.org/10.1002/chin.201519115.

Full text

APA, Harvard, Vancouver, ISO, and other styles

39

Trujillo, John, Eric Arnold, Steve Kortum, and Ralph Robinson. "Facile Synthesis of 2,4-Disubstituted Thiooxazoles and 2,4-Disubstituted Oxazole Sulfonyl Chlorides via Acyl Isothiocyanates and TMS-Diazomethane." Synlett 26, no. 12 (2015): 1764–68. http://dx.doi.org/10.1055/s-0034-1380218.

Full text

APA, Harvard, Vancouver, ISO, and other styles

40

Trujillo, John I., Eric P. Arnold, Steve Kortum, and Ralph P. Robinson. "ChemInform Abstract: Facile Synthesis of 2,4-Disubstituted Thiooxazoles and 2,4-Disubstituted Oxazole Sulfonyl Chlorides via Acyl Isothiocyanates and TMS-Diazomethane." ChemInform 46, no. 50 (2015): no. http://dx.doi.org/10.1002/chin.201550137.

Full text

APA, Harvard, Vancouver, ISO, and other styles

41

Fernández-Bolaños Guzmán, José, Salud García Rodríguez, José Fernández-Bolaños, Ma Jésus Díanez, and Amparo López-Castro. "Reaction of 2-amino-2-deoxy-d-glucose with aryl and acyl isothiocyanates, and aryl isocyanates: structure of the intermediate products." Carbohydrate Research 210 (March 1991): 125–43. http://dx.doi.org/10.1016/0008-6215(91)80117-6.

Full text

APA, Harvard, Vancouver, ISO, and other styles

42

SMOLII, O. B., S. YA PANCHISHIN, and B. S. DRACH. "ChemInform Abstract: Cyclization of Addition Products of Cyanomethylenetriphenylphosphorane with Acyl Isothiocyanates. A Convenient Route for the Preparation of Functionalized Pyrimidine Derivatives." ChemInform 25, no. 27 (2010): no. http://dx.doi.org/10.1002/chin.199427198.

Full text

APA, Harvard, Vancouver, ISO, and other styles

43

Iranpoor, N., H. Firouzabadi, and H. R. Shaterian. "REACTION OF STABLE TRIALKYLSILYL ESTERS WITH Ph3P(SCN)2: A NOVEL METHOD FOR THE PREPARATION OF ACYL AND AROYL ISOTHIOCYANATES UNDER NEUTRAL CONDITION." Synthetic Communications 32, no. 23 (2002): 3653–57. http://dx.doi.org/10.1081/scc-120014983.

Full text

APA, Harvard, Vancouver, ISO, and other styles

44

GUZMAN, J. F. B., S. G. RODRIGUEZ, J. FERNANDEZ-BOLANOS, J. DIANEZ, and A. LOPEZ-CASTRO. "ChemInform Abstract: Reaction of 2-Amino-2-deoxy-D-glucose with Aryl and Acyl Isothiocyanates, and Aryl Isocyanates: Structure of the Intermediate Products." ChemInform 23, no. 7 (2010): no. http://dx.doi.org/10.1002/chin.199207261.

Full text

APA, Harvard, Vancouver, ISO, and other styles

45

Ekram Abdullah Basheer, Kalid Matny Al-jaanaby, and Feras Shauki Al-joboury. "Synthesis a Number of Heterocyclic Compounds and some of chalcones Derived From Levofloxacin." Tikrit Journal of Pure Science 20, no. 5 (2023): 72–83. http://dx.doi.org/10.25130/tjps.v20i5.1243.

Full text

Abstract:

The hydrazide (1) was used as synthone for the following Compound pyridazine-3,6-dione (2) by reaction of hydrazide (1) with maleic anhydride and Compound phthalazine-1,4-dione (3) by the reaction of hydrazide (1) with phthalic anhydride. Substituted thiosemicarbazides (6-7) by hydrazide(1) reaction with substituted isothiocyanates in ethanol. The thiosemicarbazide (5) was, also synthesized by the reaction of hydrazide (1) with ammonium thiocyanate in presence of concentrated hydrochloric acid. 1-Formyl-2-acyl hydrazine (4) was obtained by the reaction hydrazide (1) with formic acid, and Subst

APA, Harvard, Vancouver, ISO, and other styles

46

Sadchikova, Elena V., Vasiliy A. Bakulev, Julia O. Subbotina, et al. "Synthesis and structure of new imidazo- and pyrazolo[5,1-d][1,2,3,5]thiatriazines based on the reaction of diazoazoles with acyl isothiocyanates controlled by S⋯O interaction." Tetrahedron 69, no. 34 (2013): 6987–92. http://dx.doi.org/10.1016/j.tet.2013.06.062.

Full text

APA, Harvard, Vancouver, ISO, and other styles

47

Sadchikova, Elena V., Vasiliy A. Bakulev, Julia O. Subbotina, et al. "ChemInform Abstract: Synthesis and Structure of New Imidazo- and Pyrazolo[5,1-d][1,2,3,5]thiatriazines Based on the Reaction of Diazoazoles with Acyl Isothiocyanates Controlled by S···O Interaction." ChemInform 44, no. 50 (2013): no. http://dx.doi.org/10.1002/chin.201350200.

Full text

APA, Harvard, Vancouver, ISO, and other styles

48

Trimiño, María I. García, Arturo Macías Hermán Vélez Cabrera Castro, Arístides Rosado Pérez, Dally Moya Argilagos, Anthony Linden та Heinz Heimgartner. "Reaction ofN,N'-dimethyl-2-nitroethene-1, 1-diamine with α,ß-unsaturated acyl isothiocyanates: Preparation of 1,3-thiazin-4-one and 4-nitro-1,2-thiazol-5(2H)-imine derivatives". Helvetica Chimica Acta 81, № 3-4 (1998): 718–28. http://dx.doi.org/10.1002/hlca.19980810321.

Full text

APA, Harvard, Vancouver, ISO, and other styles

49

Koch, Rainer, and Curt Wentrup. "The thioacyl isocyanate–acyl isothiocyanate rearrangement †." Journal of the Chemical Society, Perkin Transactions 2, no. 9 (2000): 1846–50. http://dx.doi.org/10.1039/b003534n.

Full text

APA, Harvard, Vancouver, ISO, and other styles

50

GARCIA TRIMINO, M. I., A. MACIAS CABRERA, H. VELEZ CASTRO та ін. "ChemInform Abstract: Reaction of N,N′-Dimethyl-2-nitroethene-1,1-diamine with α,β-Unsaturated Acyl Isothiocyanates: Preparation of 1,3-Thiazin-4-one and 4-Nitro-1,2-thiazol-5(2H)-imine Derivatives." ChemInform 29, № 29 (2010): no. http://dx.doi.org/10.1002/chin.199829056.

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!