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Original Articles

Willgerodt–Kindler reaction of arylglyoxals with amines and sulfur in aqueous media: a simple and efficient synthesis of α-ketothioamides

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Pages 464-473 | Received 16 Sep 2012, Accepted 06 Dec 2012, Published online: 22 Jan 2013

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Asha D. Jangale & Dipak S. Dalal. (2017) Green synthetic approaches for biologically relevant organic compounds. Synthetic Communications 47:23, pages 2139-2173.
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Hamid Saeidian, Saleh Vahdati-Khajehi, Homeira Bazghosha & Zohreh Mirjafary. (2014) Na2S-mediated thionation: an efficient access to secondary and tertiary α-ketothioamides via Willgerodt–Kindler reaction of readily available arylglyoxals with amines. Journal of Sulfur Chemistry 35:6, pages 700-710.
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Articles from other publishers (6)

Shubham Tiwari, Sandeep Chandrashekharappa & Guddeangadi N. Gururaja. (2023) Nucleophilic sulfur controlled efficient ketothioamide synthesis from tribromomethyl carbinols. Organic & Biomolecular Chemistry 21:42, pages 8563-8572.
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Dharmesh J. Shah, Anuj S. Sharma, Vinay S. Sharma, Vinod Kumar Vishwakarma, Achalkumar Ammathnadu Sudhakar, Pranav S. Shrivastav & Rajender S. Varma. (2023) Microcrystalline Cellulose Decorated with Fe 3 O 4 Nanoparticle Catalysts for the Microwave-Assisted Synthesis of Thioglyoxamides . ACS Applied Nano Materials 6:5, pages 4005-4016.
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N. P. Tarasova, E. G. Krivoborodov & Ya. O. Mezhuev. (2023) Nucleophilic activation of the sulfur S8 cyclic form as a green chemistry tool. Russian Chemical Bulletin 72:2, pages 415-424.
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Anjali Jaiswal, Anup Kumar Sharma, Preeti & Krishna Nand Singh. (2021) Copper‐Catalyzed Decarboxylative Synthesis of α‐Ketothioamides Using α,β‐Unsaturated Arylcarboxylic Acids, Alicyclic Secondary Amines and Elemental Sulfur. Asian Journal of Organic Chemistry 10:7, pages 1748-1751.
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Toshiaki Murai. 2019. Chemistry of Thioamides. Chemistry of Thioamides 45 73 .
Thanh Binh Nguyen & Pascal Retailleau. (2017) Methyl ketone break-and-rebuild: a strategy for full α-heterofunctionalization of acetophenones. Green Chemistry 19:22, pages 5371-5374.
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