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Volumn 5, Issue 2, 2003, Pages 145-148

Preparation of thioamide building blocks via microwave-promoted three-component kindler reactions

Author keywords

[No Author keywords available]

Indexed keywords

1 METHYL 2 PYRROLIDINONE; ALDEHYDE; AMIDE; AMINE; SOLVENT; SULFUR; THIOL DERIVATIVE; BENZALDEHYDE DERIVATIVE; DYES, REAGENTS, INDICATORS, MARKERS AND BUFFERS; MORPHOLINE DERIVATIVE; PIPERAZINE DERIVATIVE; THIOAMIDE;

EID: 0038700560     PISSN: 15204766     EISSN: None     Source Type: Journal    
DOI: 10.1021/cc0200538     Document Type: Article
Times cited : (103)

References (32)
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    • All microwave irradiation experiments were performed using the SmithSynthesizer from Personal Chemistry AB (ref 15). For a detailed description of this instrument, see the following: Stadler, A.; Kappe, C. O. J. Comb. Chem. 2001, 3, 624-630.
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    • The use of excess sulfur does not create a problem for the purity of the final thioamide product so long as the amine is also used in excess. The reactive intermediates involved in the Kindler reaction are most likely polar water-soluble nitrogen-sulfur species formed from elemental sulfur and the amine, attacking the initially formed azomethine or aminal intermediates. For details, see ref 5h and the following: Carmack, M. J. Heterocycl. Chem. 1989, 26, 1319-1323.
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    • PersonalChemistry AB, Kungsgatan 76, SE-753 18 Uppsala, Sweden. Phone: +46-18-4899000. Fax: 46-18-4899100. http://www.personalchemistry.com


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