Relevant bibliographies by topics / Aryl isothiocyanates

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Academic literature on the topic 'Aryl isothiocyanates'

Author: Grafiati
Published: 5 June 2025
Last updated: 1 August 2025

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Journal articles on the topic "Aryl isothiocyanates"

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Merola, Joseph S., та Arthur W. Grieb. "Crystal structure of chlorido(η2-phenyl isothiocyanate-κ2C,S)-mer-tris(trimethylphosphane-κP)iridium(I)". Acta Crystallographica Section E Structure Reports Online 70, № 11 (2014): 352–54. http://dx.doi.org/10.1107/s160053681402162x.

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The molecule of the title compound, [IrCl(C7H5NS)(C3H9P)3], is a distorted octahedral iridium complex with three PMe3ligands arranged in a meridional geometry, a chloride ioncisto all three PMe3groups and the phenyl isothiocyanate ligand bonded in an η2-fashion through the C and S atoms. The C atom istransto the chloride ion and the S atom is responsible for a significant deviation from an ideal octahedral geometry. The geometric parameters for the metal-complexing phenyl isothiocyanate group are compared with other metal-complexed phenyl isothiocyanates, as well as with examples of uncomplexe
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Janczewski, Łukasz, Dorota Kręgiel, and Beata Kolesińska. "Synthesis of Isothiocyanates Using DMT/NMM/TsO− as a New Desulfurization Reagent." Molecules 26, no. 9 (2021): 2740. http://dx.doi.org/10.3390/molecules26092740.

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Thirty-three alkyl and aryl isothiocyanates, as well as isothiocyanate derivatives from esters of coded amino acids and from esters of unnatural amino acids (6-aminocaproic, 4-(aminomethyl)benzoic, and tranexamic acids), were synthesized with satisfactory or very good yields (25–97%). Synthesis was performed in a “one-pot”, two-step procedure, in the presence of organic base (Et3N, DBU or NMM), and carbon disulfide via dithiocarbamates, with 4-(4,6-dimethoxy-1,3,5-triazin-2-yl)-4-methylmorpholinium toluene-4-sulfonate (DMT/NMM/TsO−) as a desulfurization reagent. For the synthesis of aliphatic
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3

Besson, Thierry, Jérôme Guillard, Charles W. Rees, and Valérie Thiéry. "New syntheses of aryl isothiocyanates †." Journal of the Chemical Society, Perkin Transactions 1, no. 5 (1998): 889–92. http://dx.doi.org/10.1039/a707801c.

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4

Sandeep, K., Alla Siva Reddy, and K. C. Kumara Swamy. "Cu(i) catalysed annulation of isothiocyanates/isocyanates with 2-iodo-sulfonamides: synthesis of benzodithiazines, benzothiadiazinones, benzothiazinylidene-anilines and benzothiazolylidene-anilines." Organic & Biomolecular Chemistry 17, no. 28 (2019): 6880–94. http://dx.doi.org/10.1039/c9ob00994a.

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Tanimori, Shinji, Haruna Nariki, Takuya Miyamura, Daiki Matsui, and Motohiro Sonoda. "Iodine-Mediated Facile One-Pot Access to N-Aryl-2-benzoxazolamines." SynOpen 04, no. 04 (2020): 99–106. http://dx.doi.org/10.1055/s-0040-1705982.

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AbstractFacile, iodine-mediated access to N-aryl-2-benzoxazolamines has been achieved in a one-pot manner under mild reaction conditions. Reaction of 2-aminophenols and aryl isothiocyanates afforded N-aryl-2-benzoxazolamines in the presence of molecular iodine and pyridine in tetrahydrofuran at room temperature in moderate to excellent yields.
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V. Yadgire, Atul, Gajanan V. Korpe, and Shirish P. Deshmukh. "Comparative Study of Microwave Induced and Conventional Synthesis of Acetylated Sugar Isothiocyanates and Related Thiocarbamides." E-Journal of Chemistry 8, no. 4 (2011): 1614–19. http://dx.doi.org/10.1155/2011/473646.

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The synthesis of several acetylated sugar isothiocyanates have been carried out under microwave irradiation in excellent yields of products by using related bromides and lead thiocyanate in sodium dried xylene. Several acetylated sugar thiocarbamides have been synthesized by the interaction of respective acetylated sugar isothiocyanates with appropriate aryl amines under microwave irradiation.
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7

Mamta, T. Sangole, and P. Deshmukh Shirish. "Synthesis and characterization of 1-hepta-O-benzoyl-ß-D-maltosyl-5-aryl-2-Sbenzyl- 2,4-isodithiobiurets." Journal of Indian Chemical Society Vol. 88, May 2011 (2011): 743–46. https://doi.org/10.5281/zenodo.5769143.

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P.G. Department of Chemistry, Shri Shivaji College, Akola-444 001, Maharashtra, India <em>E-mail</em>: mamtasangole@rediffmail.com <em>Manuscript received 09 January 2009, revised 08 September 2010, accepted 15 September 2010</em> A series of novel 1-hepta-0-benzoyi-P-o-maltosyl-5-aryi-2-S-benzyl-2,4-isodithiobiurets have been synthesized by the interaction of 1-hepta-&beta;-benzoyl-P-D-maltosyl-S-benzyl isothiocarbamlde with various aryl isothiocyanates. The newly synthesized compounds have been characterized by analytical and IR, <sup>1</sup>H NMR and Mass spectral studies.
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He, Yimiao, Jing Li, Shuang Luo, Jinbo Huang, and Qiang Zhu. "A metal-free synthesis of 2-aminobenzothiazoles through aminyl radical addition to aryl isothiocyanates." Chemical Communications 52, no. 54 (2016): 8444–47. http://dx.doi.org/10.1039/c6cc04394a.

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9

Yadav, Arvind K., and Lal Dhar S. Yadav. "Direct construction of 2-alkylbenzo-1,3-azoles via C–H activation of alkanes for C–C and C–X (X = O, S) bond formation." Organic & Biomolecular Chemistry 13, no. 9 (2015): 2606–11. http://dx.doi.org/10.1039/c4ob02488e.

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Sun, Nan, Bin Li, Jianping Shao, et al. "A general and facile one-pot process of isothiocyanates from amines under aqueous conditions." Beilstein Journal of Organic Chemistry 8 (January 10, 2012): 61–70. http://dx.doi.org/10.3762/bjoc.8.6.

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A general and facile one-pot protocol for the preparation of a broad range of alkyl and aryl isothiocyanates has been developed from their corresponding primary amines under aqueous conditions. This synthetic process involves an in situ generation of a dithiocarbamate salt from the amine substrate by reacting with CS2 followed by elimination to form the isothiocyanate product with cyanuric acid as the desulfurylation reagent. The choice of solvent is of decisive importance for the successful formation of the dithiocarbamate salt particularly for highly electron-deficient substrates. This novel
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Book chapters on the topic "Aryl isothiocyanates"

1

Braverman, S., M. Cherkinsky, and M. L. Birsa. "Alkyl and Aryl Isothiocyanates." In Four Carbon-Heteroatom Bonds. Georg Thieme Verlag KG, 2005. http://dx.doi.org/10.1055/sos-sd-018-00231.

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Faulkner, S., R. C. Whitehead, and R. J. Aarons. "Reaction of 2-Acylketene Dithioacetals with Aryl Isothiocyanates." In Six-Membered Hetarenes with One Chalcogen. Georg Thieme Verlag KG, 2003. http://dx.doi.org/10.1055/sos-sd-014-00936.

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Argyropoulos, N. G. "Heterapentalenes from -Aryl-3-imino-3-1,2,4-dithiazol-5-amines and Aryl Isothiocyanates." In Five-Membered Hetarenes with Three or More Heteroatoms. Georg Thieme Verlag KG, 2004. http://dx.doi.org/10.1055/sos-sd-013-00080.

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Argyropoulos, N. G. "Heterapentalenes from 1,2,3,4-Thiatriazol-5-amines and Aryl Isothiocyanates." In Five-Membered Hetarenes with Three or More Heteroatoms. Georg Thieme Verlag KG, 2004. http://dx.doi.org/10.1055/sos-sd-013-00072.

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Ulrich, H. "From Alkyl [(3-Phenyl-2-propynoyl)anilino]acetates and Aryl Isothiocyanates." 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-017-00189.

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Currell, Douglas L. "[18] Derivatives of hemoglobin prepared by reaction with aryl or alkyl isothiocyanates." In Hemoglobins Part B: Biochemical and Analytical Methods. Elsevier, 1994. http://dx.doi.org/10.1016/0076-6879(94)31020-3.

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Kikelj, D. "From -Arylguanidines, -Arylbenzimidamides, or -Arylisothioureas and Aryl Isothiocyanates, 4-Tosylcarbonimidic Dichloride, Phosgene, Alkyl Chloroformates, or Carbon Monoxide." In Six-Membered Hetarenes with Two Identical Heteroatoms. Georg Thieme Verlag KG, 2004. http://dx.doi.org/10.1055/sos-sd-016-00811.

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Conference papers on the topic "Aryl isothiocyanates"

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Kioko, Stephen M., and Ward G. Kirlin. "Abstract 4066: Benzyl isothiocyanate causes degradation of the aryl hydrocarbon receptor in hepa1c1c7 cells." In Proceedings: AACR 101st Annual Meeting 2010‐‐ Apr 17‐21, 2010; Washington, DC. American Association for Cancer Research, 2010. http://dx.doi.org/10.1158/1538-7445.am10-4066.

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Kioko, Stephen M., Michael D. Powell, and Ward G. Kirlin. "Abstract 1850: Benzyl isothiocyanate causes proteasome-mediated degradation of aryl hydrocarbon receptor in Hepa1c1c7 cells." In Proceedings: AACR 102nd Annual Meeting 2011‐‐ Apr 2‐6, 2011; Orlando, FL. American Association for Cancer Research, 2011. http://dx.doi.org/10.1158/1538-7445.am2011-1850.

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