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Synthetic Communications
An International Journal for Rapid Communication of Synthetic Organic Chemistry
Volume 40, 2010 - Issue 3
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Original Articles

Efficient Thiocyanation of Indoles Using Para-Toluene Sulfonic Acid

Biswanath Das Organic Chemistry Division I, Indian Institute of Chemical Technology, Hyderabad, Andhra Pradesh, IndiaCorrespondence[email protected]
&
Avula Satya Kumar Organic Chemistry Division I, Indian Institute of Chemical Technology, Hyderabad, Andhra Pradesh, India
Pages 337-341 | Received 27 Dec 2008, Published online: 06 Jan 2010

Citations (15)

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Sobhan Rezayati, Fatemeh Kalantari, Ali Ramazani & Elham Ezzatzadeh. (2021) Isoquinolinium-N-sulfonic acid thiocyanate/H2O2 as efficient reagent for thiocyanation of N-bearing (hetero)aromatic compounds. Journal of Sulfur Chemistry 42:5, pages 575-590.
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Mohammad Ali Karimi Zarchi & Reza Banihashemi. (2016) Thiocyanation of aromatic and heteroaromatic compounds using polymer-supported thiocyanate ion as the versatile reagent and ceric ammonium nitrate as the versatile single-electron oxidant. Journal of Sulfur Chemistry 37:3, pages 282-295.
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V. Sudhakar Chary, G. Krishnaiah, M. Satish Kumar & K. C. Rajanna. (2015) Zeolite H-Sdusy Powder (Cbv720) as a Recyclable Catalyst for an Efficient Thiocyanation of Aromatic and Heteroaromatic Compounds in Acetonitrile. Phosphorus, Sulfur, and Silicon and the Related Elements 190:7, pages 1146-1153.
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Mohammad Ali, Karimi Zarchi & R. Banihashemi. (2014) Green and Efficient Method for Thiocyanation of Aromatic and Heteroaromatic Compounds Using Cross-linked Poly (4-Vinylpyridine) Supported Thiocyanate Ion as Versatile Reagent and Oxone as Mild Oxidant. Phosphorus, Sulfur, and Silicon and the Related Elements 189:9, pages 1378-1390.
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M. A. Karimi Zarchi & R. Banihashemi. (2014) An efficient and regioselective thiocyanation of aromatic and heteroaromatic compounds using cross-linked poly (4-vinylpyridine)-supported thiocyanate as a versatile reagent and potassium peroxydisulfate as a strong oxidizing agent. Journal of Sulfur Chemistry 35:4, pages 458-469.
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Liqiang Wu, Shujun Chao, Xiao Wang & Fulin Yan. (2011) Poly[4-diacetoxyiodo] Styrene–Promoted Thiocyanation of Aromatic Ethers, Anilines, and Indoles. Phosphorus, Sulfur, and Silicon and the Related Elements 186:2, pages 304-310.
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Articles from other publishers (9)

Bhargav Desai, Piyushkumar Satani, Rachit S. Patil, Hussain Bhukya & Togati Naveen. (2023) Microwave‐Assisted Metal‐Free C(sp 2 )−H Thiocyanation of Aromatic Amines . ChemistrySelect 8:30.
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Da-Liang Zhu, Haoyu Wen, Qi Wu, Jie Li, David J. Young, Yanqing Wang & Hong-Xi Li. (2023) Exogenous photocatalyst- and metal-free photoinduced C-3 thiocyanation of indoles using O2 as the oxidant. Tetrahedron 135, pages 133322.
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Boris V. Lyalin, Vera L. Sigacheva, Anastasia S. Kudinova, Sergey V. Neverov, Vladimir A. Kokorekin & Vladimir A. Petrosyan. (2021) Electrooxidation Is a Promising Approach to Functionalization of Pyrazole-Type Compounds. Molecules 26:16, pages 4749.
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Chitteti Divyavani, Pannala Padmaja, Vinod G. Ugale & Pedavenkatagari Narayana Reddy. (2021) A Review on Thiocyanation of Indoles. Current Organic Synthesis 18:3, pages 233-247.
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Sobhan Rezayati & Ali Ramazani. (2020) A review on electrophilic thiocyanation of aromatic and heteroaromatic compounds. Tetrahedron 76:36, pages 131382.
Crossref
Dariush Khalili. (2015) Highly efficient and regioselective thiocyanation of aromatic amines, anisols and activated phenols with H2O2/NH4SCN catalyzed by nanomagnetic Fe3O4. Chinese Chemical Letters 26:5, pages 547-552.
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Weigang Fan, Qi Yang, Fengshan Xu & Pixu Li. (2014) A Visible-Light-Promoted Aerobic Metal-Free C-3 Thiocyanation of Indoles. The Journal of Organic Chemistry 79:21, pages 10588-10592.
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Bruna L. Kuhn, Margiani P. Fortes, Teodoro S. Kaufman & Claudio C. Silveira. (2014) Facile, efficient and eco-friendly synthesis of 5-sulfenyl tetrazole derivatives of indoles and pyrroles. Tetrahedron Letters 55:9, pages 1648-1652.
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Biswanath Das & Avula Satya Kumar. (2010) ChemInform Abstract: Efficient Thiocyanation of Indoles Using para‐Toluene Sulfonic Acid.. ChemInform 41:26.
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