Heterocyclization of 3-deoxy-d-erythro-hexos-2-ulose-1,2-bis(thiosemicarbazone). Crystal structure of the major diastereomer
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Biochemistry,General Medicine,Analytical Chemistry
Reference26 articles.
1. Synthesis, spectroscopic characterization and biological properties of new natural aldehydes thiosemicarbazones
2. Reversed-phase high-performance liquid chromatography of 4-(2-pyridyl)-1-piperazinethiocarboxylic acid 2-[1-(pyridyl)ethylidene]hydrazide dihydrochloride (NSC 348977), a synthetic thiosemicarbazone with antitumor activity
3. Behavior of free sugar thiosemicarbazones toward heterocyclization reactions
4. Structure and reactions of aldose semicarbazone and thiosemicarbazone derivatives under acetylating conditions
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2. Desulfurization processes of thiosemicarbazonecopper(ii) derivatives in acidic and basic aqueous media;New Journal of Chemistry;2013
3. Facile one-pot synthesis of sugar–thiazolidinone derivatives;Canadian Journal of Chemistry;2011-11
4. Chemistry and heterocyclization of thiosemicarbazones;Journal of Heterocyclic Chemistry;2011-10-18
5. Synthesis and antiacetylcholinesterase activity of new D-glyceraldehyde heterocyclic derivatives;Journal of the Brazilian Chemical Society;2010
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