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Phosphorus, Sulfur, and Silicon and the Related Elements Volume 180, 2005 - Issue 2
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Original Articles

Reactions of Cyanothioformamide and Thiohydantoin Derivatives With Some Arylidenes of Cyanothioacetamide and Other Elecetrophilic and Nucleophilic Reagents

A. M. Sh. El-Sharief Chemistry Department, Faculty of Science, Al-Azhar University (for Boys), Cairo, Egypt
,
F. F. Mahmoud Chemistry Department, Faculty of Science, Al-Azhar University (for Girls), Cairo, Egypt
,
N. M. Taha Chemistry Department, Faculty of Science, Al-Azhar University (for Girls), Cairo, Egypt
&
E. M. Ahmed Chemistry Department, Faculty of Science, Al-Azhar University (for Girls), Cairo, Egypt
Pages 573-589 | Received 01 Jun 2004, Published online: 21 Dec 2010

Citations (14)

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Read on this site (5)

Samir Y. Abbas, Marwa A. M. Sh. El-Sharief, Mohamed A. Salem & Ahmed M. Sh. El-Sharief. (2020) Utilization of cyanothioformamides in the syntheses of various types of imidazole derivatives. Synthetic Communications 50:5, pages 621-648.
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Hélène G. Bazin, Laura S. Bess & Mark T. Livesay. (2018) Synthesis and Applications of Imidazoquinolines: A Review. Organic Preparations and Procedures International 50:2, pages 109-244.
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Mohamed A. Metwally & Ehab Abdel-Latif. (2012) Thiohydantoins: synthetic strategies and chemical reactions. Journal of Sulfur Chemistry 33:2, pages 229-257.
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A.M. Sh. El-Sharief & S.Y. Al-Raqa. (2007) New Types of Mono and Bis Sulfonamides, Tosylamino Acids and Thiosulfonic Ester Derived from Xanthotoxin, Bergapten and Visnagin with Biological Interest. Phosphorus, Sulfur, and Silicon and the Related Elements 182:7, pages 1557-1580.
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AhmedM. Sh. El-Sharief, Abdulkhaliq M. Al-Amri & Shaya Y. Al-Raqa. (2006) Halogenated, alkylated and new types of imidazolidine, pyrrolidine, imidazotriazine and thienoimidazole derivatives with biological and antitumor activities. Journal of Sulfur Chemistry 27:3, pages 245-263.
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Articles from other publishers (9)

Ziad Moussa, Zaher M. A. JudehMarwa A. M. Sh. El‐Sharief & Ahmed M. Sh. El‐Sharief. (2020) N ‐Arylcyanothioformamides: Preparation Methods and Application in the Synthesis of Bioactive Molecules . ChemistrySelect 5:2, pages 764-798.
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Marwa A. M. Sh. El-Sharief, Ziad Moussa & Ahmed M. Sh. El-Sharief. (2013) Synthesis and Biological Evaluation of Bis-Imidazolidineiminothiones: A Comparative Study. Archiv der Pharmazie 346:7, pages 542-555.
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Marwa A.M.Sh. El-Sharief, Ziad Moussa & Ahmed M.Sh. El-Sharief. (2011) Synthesis, characterization, and derivatization of some novel types of fluorinated mono- and bis-imidazolidineiminothiones with antitumor, antiviral, antibacterial, and antifungal activities. Journal of Fluorine Chemistry 132:9, pages 596-611.
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Ashok Kumar, Pratibha Sharma, Prerna Kumari & Bhagwan Lal Kalal. (2011) Exploration of antimicrobial and antioxidant potential of newly synthesized 2,3-disubstituted quinazoline-4(3H)-ones. Bioorganic & Medicinal Chemistry Letters 21:14, pages 4353-4357.
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Ziad Moussa, Marwa A.M.Sh. El-Sharief & Ahmed M.Sh. El-Sharief. (2011) Synthesis and characterization of new types of halogenated and alkylated imidazolidineiminothiones and a comparative study of their antitumor, antibacterial, and antifungal activities. European Journal of Medicinal Chemistry 46:6, pages 2280-2289.
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Panayiotis A. Koutentis & Sophia S. Michaelidou. (2010) The conversion of 2-cyano cyanothioformanilides into 3-aminoindole-2-carbonitriles using triphenylphosphine. Tetrahedron 66:32, pages 6032-6039.
Crossref
A.J. Moore. 2008. Comprehensive Heterocyclic Chemistry III. Comprehensive Heterocyclic Chemistry III 65 127 .
Shaya Y. Al-Raqa, Ahmed M. Sh. ElSharief, Saied M. E. Khalil & Abdulkhaliq M. Al-Amri. (2006) Synthesis of some novel imidazolidine derivatives and their metal complexes with biological and antitumor activity. Heteroatom Chemistry 17:7, pages 634-647.
Crossref
A. M. Sh. El‐Sharief, F. F. Mahmoud, N. M. Taha & E. M. Ahmed. (2005) Reactions of Cyanothioformamide and Thiohydantoin Derivatives with Some Arylidenes of Cyanothioacetamide and Other Electrophilic and Nucleophilic Reagents.. ChemInform 36:26.
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