Regioselective reduction of 2-cyanoprop-2-enethioamides with sodium borohydride

Dotsenko, V. V.; Кривоколыско, С. Г.

doi:10.1007/s11172-012-0321-1

Russ Chem Bull

2012

DOI: 10.1007/s11172-012-0321-1

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Regioselective reduction of 2-cyanoprop-2-enethioamides with sodium borohydride

V. V. Dotsenko

С. Г. Кривоколыско

Abstract: Treatment of 2 cyanoprop 2 enethioamides with NaBH 4 in EtOH gave C alkylated cyano thioacetamides in 62-69% yields.

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Cited by 6 publications

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Synthesis of partially hydrogenated 1,3,5-thiadiazines by Mannich reaction

Dotsenko

Фролов

Кривоколыско

2015

Chem Heterocycl Comp

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Regioselective reduction of 2-cyanoprop-2-enethioamides with sodium borohydride

Abstract: Treatment of 2 cyanoprop 2 enethioamides with NaBH 4 in EtOH gave C alkylated cyano thioacetamides in 62-69% yields.

Cited by 6 publications

References 15 publications

Synthesis of partially hydrogenated 1,3,5-thiadiazines by Mannich reaction

Synthesis of partially hydrogenated 1,3,5-thiadiazines by Mannich reaction

Aminomethylation of morpholinium and N-methylmorpholinium 3,5-dicyano-4,4-dimethyl-6-oxo-1,4,5,6-tetrahydropyridine-2-thiolates

Synthesis, structure, and reactions of (4-aryl-3-cyano-6-oxopiperidin-2-ylidene)malononitriles

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