http://www.cnr.it/ontology/cnr/individuo/prodotto/ID213820
Astraightforward synthetic access to symmetrical glycosyl disulfides and biological evaluation thereof (Articolo in rivista)
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- Label
- Astraightforward synthetic access to symmetrical glycosyl disulfides and biological evaluation thereof (Articolo in rivista) (literal)
- Anno
- 2011-01-01T00:00:00+01:00 (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
- 10.1039/c1ob05619k (literal)
- Alternative label
Adinolfi M, Capasso D, Di Gaetano S, Iadonisi A, Leone L, Pastore A (2011)
Astraightforward synthetic access to symmetrical glycosyl disulfides and biological evaluation thereof
in Organic & biomolecular chemistry
(literal)
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- Adinolfi M, Capasso D, Di Gaetano S, Iadonisi A, Leone L, Pastore A (literal)
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- Dipartimento di Chimica Organica e Biochimica, Università Federico II di Napoli, Naples, Italy. (literal)
- Titolo
- Astraightforward synthetic access to symmetrical glycosyl disulfides and biological evaluation thereof (literal)
- Abstract
- Symmetrical glycosyl disulfides can be prepared within a few hours from per-O-acetylated precursors via a sequential approach entailing short reactions and no purification of any intermediate. The final thiolate-to-disulfide oxidation step is noticeably accelerated by low amounts of phenyl diselenide under air. Applicability of the strategy to non-saccharidic symmetrical alkyl disulfides has also been examined. A preliminary assay of the cytotoxic activity of symmetrical 1,1'- disulfides was performed on two human tumor cell lines, and a noteworthy activity was recorded for a range of these synthetic compounds. (literal)
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