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Synthetic Communications
An International Journal for Rapid Communication of Synthetic Organic Chemistry
Volume 25, 1995 - Issue 21
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Original Articles

A Convenient Route to Substituted Thiocarbamides

Krishnamurthy Ramadas Centre For Agrochemical Research SPIC Science Foundation, 110, Mount Road, Guindy, Madras, 600 032, INDIA
&
Natarajan Srinivasan Centre For Agrochemical Research SPIC Science Foundation, 110, Mount Road, Guindy, Madras, 600 032, INDIA
Pages 3381-3387 | Received 20 Mar 1995, Published online: 23 Sep 2006

Citations (15)

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Ferenc Kardon, Mária Mörtl & Gábor Magyarfalvi. (2008) Preparation of Mixed Carbamic/Dithiocarbamic Anhydrides via Silyl Carbamates or Silyl Dithiocarbamates. Synthetic Communications 38:2, pages 192-199.
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K. Ramadas & N. Janarthanan. (1997) New Synthetic Strategy for Urea Herbicides. Synthetic Communications 27:13, pages 2357-2362.
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Articles from other publishers (13)

Prasanna Kumar Ganta, Mallemadugula Ravi Teja, Chun-Juei Chang, Anandan Sambandam, Rajiv Kamaraj, Yu-Ting Chu, Shangwu Ding, Hsing-Yin Chen & Hsuan-Ying Chen. (2023) Improvement of catalytic activity of aluminum complexes for the ring-opening polymerization of ε-caprolactone: aluminum thioamidate and thioureidate systems. Dalton Transactions 52:46, pages 17132-17147.
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Zhuo-Bin Huang, Xiong-Jian Xia, Zi-Hao Huang, Li Xu, Xiao-Yong Zhang & Ri-Yuan Tang. (2020) Selective C–H dithiocarbamation of arenes and antifungal activity evaluation. Organic & Biomolecular Chemistry 18:7, pages 1369-1376.
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Franz Steppeler, Dominika Iwan, Elżbieta Wojaczyńska & Jacek Wojaczyński. (2020) Chiral Thioureas—Preparation and Significance in Asymmetric Synthesis and Medicinal Chemistry. Molecules 25:2, pages 401.
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Chaochao Ding, Shaoli Wang, Yaoguang Sheng, Qian Dai, Yunjie Zhao, Guang Liang & Zengqiang Song. (2019) One-step construction of unsymmetrical thioureas and oxazolidinethiones from amines and carbon disulfide via a cascade reaction sequence . RSC Advances 9:46, pages 26768-26772.
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Soumya Dutta, Manas Mondal, Tubai Ghosh & Amit Saha. (2019) Unprecedented thiocarbamidation of nitroarenes: a facile one-pot route to unsymmetrical thioureas. Organic Chemistry Frontiers 6:1, pages 70-74.
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Hamid Beyzaei, Somaye Kooshki, Reza Aryan, Mohammad Mehdi Zahedi, Alireza Samzadeh-Kermani, Behzad Ghasemi & Mohammadreza Moghaddam-Manesh. (2017) MgO Nanoparticle-Catalyzed Synthesis and Broad-Spectrum Antibacterial Activity of Imidazolidine- and Tetrahydropyrimidine-2-Thione Derivatives. Applied Biochemistry and Biotechnology 184:1, pages 291-302.
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Qiang Cao, Fang Liu, Min Wang, Wan Xu, Meng-Tian Zeng, Min Liu, Yue-Sheng Li & Zhi-Bing Dong. (2017) Facile synthesis of substituted arylthioureas in the presence of sodium hydride. Journal of Chemical Research 41:5, pages 301-303.
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Xing Liu, Min Liu, Wan Xu, Meng-Tian Zeng, Hui Zhu, Cai-Zhu Chang & Zhi-Bing Dong. (2017) An environmentally benign and efficient synthesis of substituted benzothiazole-2-thiols, benzoxazole-2-thiols, and benzimidazoline-2-thiones in water. Green Chemistry 19:23, pages 5591-5598.
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Alan R. Katritzky, Stephane Ledoux, Rachel M. Witek & Satheesh K. Nair. (2004) 1-(Alkyl/Arylthiocarbamoyl)benzotriazoles as Stable Isothiocyanate Equivalents:  Synthesis of Di- and Trisubstituted Thioureas. The Journal of Organic Chemistry 69:9, pages 2976-2982.
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Pramod K. Mohanta, Sanchita Dhar, S.K. Samal, H. Ila & H. Junjappa. (2000) 1-(Methyldithiocarbonyl)imidazole: a Useful Thiocarbonyl Transfer Reagent for Synthesis of Substituted Thioureas. Tetrahedron 56:4, pages 629-637.
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Mamoru Koketsu, Norihito Suzuki & Hideharu Ishihara. (1999) Preparation of Isoselenocyanate and Synthesis of Carbodiimide by Oxidation of Selenourea. The Journal of Organic Chemistry 64:17, pages 6473-6475.
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Krishnamurthy Ramadas, Govindaraghavan Suresh, Narayanasamy Janarthanan & Selladurai Masilamani. (1998) Antifungal activity of 1,3-disubstituted symmetrical and unsymmetrical thioureas. Pesticide Science 52:2, pages 145-151.
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K. RAMADAS & N. SRINIVASAN. (2010) ChemInform Abstract: A Convenient Route to Substituted Thiocarbamides.. ChemInform 27:3.
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