Relevant bibliographies by topics / Acyl isothiocyanates

Contents

  1. Journal articles
  2. Book chapters

Academic literature 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 lists of relevant articles, books, theses, conference reports, and other scholarly sources 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.

Journal articles on the topic "Acyl isothiocyanates"

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.&nbsp;</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
More sources

Book chapters on the topic "Acyl isothiocyanates"

1

Hemming, K. "Via -Acylamidoximes Derived from -Acyl Isothiocyanates." In Five-Membered Hetarenes with Three or More Heteroatoms. Georg Thieme Verlag KG, 2004. http://dx.doi.org/10.1055/sos-sd-013-00187.

Full text
APA, Harvard, Vancouver, ISO, and other styles
2

von Angerer, S. "Reaction of Enamines with Acyl Isothiocyanates." In Science of Synthesis Knowledge Updates KU 2011/1. Georg Thieme Verlag KG, 2011. http://dx.doi.org/10.1055/sos-sd-116-00223.

Full text
APA, Harvard, Vancouver, ISO, and other styles
3

von Angerer, S. "Reaction of Enamines with Acyl Isothiocyanates." In Six-Membered Hetarenes with Two Identical Heteroatoms. Georg Thieme Verlag KG, 2004. http://dx.doi.org/10.1055/sos-sd-016-00578.

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

von Angerer, S. "Reaction of Acyl Isothiocyanates with Amidine Derivatives." In Six-Membered Hetarenes with Two Unlike or More than Two Heteroatoms and Fully Unsaturated Larger-Ring Heterocycles. Georg Thieme Verlag KG, 2004. http://dx.doi.org/10.1055/sos-sd-017-00781.

Full text
APA, Harvard, Vancouver, ISO, and other styles
You might also be interested in the extended bibliographies on the topic 'Acyl isothiocyanates' for particular source types:
Journal articles
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