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Synthetic Communications
An International Journal for Rapid Communication of Synthetic Organic Chemistry
Volume 29, 1999 - Issue 8
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Original Articles

Solventless Regeneration of Ketones from Thioketones using Clay Supported Nitrate Salts and Microwave Irradiation

Rajender S. Varma Department of Chemistry and Texas Research Institute for Environmental Studies Sam Houston State University, Huntsville, TX, 77341-2117, USA E-mail: [email protected]
&
Dalip Kumar Department of Chemistry and Texas Research Institute for Environmental Studies Sam Houston State University, Huntsville, TX, 77341-2117, USA E-mail: [email protected]
Pages 1333-1340 | Received 13 Oct 1998, Published online: 17 Sep 2007

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Masoud Nasr-Esfahani, Morteza Montazerozohori, Majid Moghadam, Iraj Mohammadpoor-Baltork & Sareh Moradi. (2010) Transformation of Thioamide Compounds to Corresponding Amides Using 12-Tungstosilicic Acid. Phosphorus, Sulfur, and Silicon and the Related Elements 185:2, pages 261-266.
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Masoud Nasr-Esfahani, Majid Moghadam, Iraj Mohammadpoor-Baltork & Mohammad Hasan Boostanifar. (2009) Acidified, Wet, Silica-Supported Tetrabutylammonium Periodate: A Convenient and Mild Reagent for Conversion of Thioamides to Their Corresponding Amides Under Solvent-Free Conditions. Phosphorus, Sulfur, and Silicon and the Related Elements 184:8, pages 2004-2009.
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Masoud Nasr-Esfahani, Morteza Montazerozohori, Majid Moghadam, Iraj Mohammadpoor-Baltork & Sareh Moradi. (2009) A convenient and inexpensive method for conversion of thioamide compounds to their oxo derivatives using acidified iodine monochloride. Journal of Sulfur Chemistry 30:1, pages 17-21.
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Masoud Nasr-Esfahani, Majid Moghadam, Iraj Mohammadpoor-Baltork & Mohammad Hasan Boostanifar. (2008) A Mild and Convenient Method for Conversion of Thioamides to Their Corresponding Amides Using Acidified Wet Silica-Supported Permanganate Under Solvent-Free Conditions. Phosphorus, Sulfur, and Silicon and the Related Elements 184:1, pages 141-146.
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Xicun Wang, Zheng Li, Zhengjun Quan, Xinsheng Lu & Ruhu Gou. (2003) Solvent-Free Synthesis of 2-Furyl-5-aryloxyacetylamido-1,3,4-thiadiazoles Under Microwave Irradiation. Synthetic Communications 33:16, pages 2891-2897.
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Iraj Mohammadpoor-Baltork, Majid M. Sadeghi & Karim Esmayilpour. (2003) A Convenient and Inexpensive Method for Conversion of Thiocarbonyl Compounds to Their Oxo Derivatives Using Oxone Under Solvent-Free Conditions. Synthetic Communications 33:6, pages 953-959.
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Articles from other publishers (20)

Behnam Gholipour, Salman Shojaei, Sadegh Rostamnia, Mohammad Reza Naimi-Jamal, Dokyoon Kim, Taras Kavetskyy, Nasrin Nouruzi, Ho Won Jang, Rajender S. Varma & Mohammadreza Shokouhimehr. (2021) Metal-free nanostructured catalysts: sustainable driving forces for organic transformations. Green Chemistry 23:17, pages 6223-6272.
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Atefeh Roosta, Abdolali Alizadeh, Reze Rezaiyehraad & Mojtaba Khanpour. (2020) Efficient and Chemoselective Procedure for Conversion of Rhodanine Derivatives into 1,3‐Thiazolidine‐2,4‐diones via 1,3‐Dipolar Cycloaddition Reaction and Rearrangement Sequences. ChemistrySelect 5:40, pages 12531-12534.
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Sainath Zangade & Pravinkumar Patil. (2020) A Review on Solvent-free Methods in Organic Synthesis. Current Organic Chemistry 23:21, pages 2295-2318.
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Rajender S. Varma. 2001. Kirk-Othmer Encyclopedia of Chemical Technology. Kirk-Othmer Encyclopedia of Chemical Technology 1 68 .
Rajender S. Varma & R. B. Nasir Baig. 2012. Microwaves in Organic Synthesis. Microwaves in Organic Synthesis 425 486 .
Kiumars Bahrami, Mohammad M. Khodaei & Azita Farrokhi. (2009) H2O2/SOCl2: a useful reagent system for the conversion of thiocarbonyls to carbonyl compounds. Tetrahedron 65:36, pages 7658-7661.
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Moslem M. Lakouraj & Keivan Ghodrati. (2008) A facile and convenient method for the conversion of thioamides into amides using pyridinium hydrobromide perbromide. Monatshefte für Chemie - Chemical Monthly 139:5, pages 549-551.
Crossref
Rajender S. Varma & Yuhong Ju. 2006. Microwaves in Organic Synthesis. Microwaves in Organic Synthesis 362 415 .
J.M. Adams & R.W. McCabe. 2006. Handbook of Clay Science. Handbook of Clay Science 541 581 .
E.S.H. El Ashry, A.A. Kassem & E. Ramadan. 2006. Advances in Heterocyclic Chemistry Volume 90. Advances in Heterocyclic Chemistry Volume 90 1 123 .
C.E. Foster & P.R. Mackie. 2005. Comprehensive Organic Functional Group Transformations II. Comprehensive Organic Functional Group Transformations II 215 266 .
V. K. Ahluwalia & M. KidwaiV. K. Ahluwalia & M. Kidwai. 2004. New Trends in Green Chemistry. New Trends in Green Chemistry 59 72 .
Rajender S. Varma. 2001. Kirk-Othmer Encyclopedia of Chemical Technology. Kirk-Othmer Encyclopedia of Chemical Technology.
. (2003) Transformation of Thiocarbonyls to Their Corresponding Carbonyl Compounds Using n-Butyltriphenylphosphonium Dichromate (Bu n PPh 3 ) 2 Cr 2 O 7 in Solution and under Microwave Irradiation . Bulletin of the Korean Chemical Society 24:7, pages 1002-1004.
Crossref
Michael B. Smith. 2003. Compendium of Organic Synthetic Methods. Compendium of Organic Synthetic Methods 386 416 .
Iraj Mohammadpoor-Baltork, Majid M. M. Sadeghi & Karim Esmayilpour. (2019) Convenient Transformation of Thiocarbonyl to Carbonyl Group Using Benzyltriphenylphosphonium and n -Butyltriphenylphosphonium Peroxodisulfates . Journal of Chemical Research 2003:6, pages 348-350.
Crossref
Iraj Mohammadpoor-Baltork, Mohammad Mehdi Khodaei & Kobra Nikoofar. (2003) Bismuth(III) nitrate pentahydrate: a convenient and selective reagent for conversion of thiocarbonyls to their carbonyl compounds. Tetrahedron Letters 44:3, pages 591-594.
Crossref
Rajender S. Varma. (2002) Clay and clay-supported reagents in organic synthesis. Tetrahedron 58:7, pages 1235-1255.
Crossref
Pelle Lidström, Jason Tierney, Bernard Wathey & Jacob Westman. (2001) Microwave assisted organic synthesis—a review. Tetrahedron 57:45, pages 9225-9283.
Crossref
Rajender S. Varma & Dalip Kumar. (2010) ChemInform Abstract: Solventless Regeneration of Ketones from Thioketones Using Clay Supported Nitrate Salts and Microwave Irradiation.. ChemInform 30:28.
Crossref

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