http://www.cnr.it/ontology/cnr/individuo/prodotto/ID16795
A New Versatile and Diastereoselective Synthesis of Polysubstituted 2-Oxopiperazines from Naturally Occurring Amino Acids (Articolo in rivista)
- Type
- Label
- A New Versatile and Diastereoselective Synthesis of Polysubstituted 2-Oxopiperazines from Naturally Occurring Amino Acids (Articolo in rivista) (literal)
- Anno
- 2007-01-01T00:00:00+01:00 (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
- 10.1016/j.tetasy.2007.10.027 (literal)
- Alternative label
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
- Reginato G.; Di Credico B.; Andreotti D.; Mingardi A.; Paio A.; Donati D. (literal)
- Pagina inizio
- Pagina fine
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroVolume
- Rivista
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- Note
- ISI Web of Science (WOS) (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#affiliazioni
- Andreotti D.; Mingardi A.; Paio A.; Donati D.
GlaxoSmithKline, Medicine Research Centre, Via A. Fleming 4, 37135 Verona, Italy (literal)
- Titolo
- A New Versatile and Diastereoselective Synthesis of Polysubstituted 2-Oxopiperazines from Naturally Occurring Amino Acids (literal)
- Abstract
- A highly stereoselective approach to 1,3,4,5- and 1,3,30,4,5-polysubstituted 2-oxopiperazines is reported. The method is based on the synthetic elaboration of naturally occurring amino acids to obtain enantiomerically enriched C-5 substituted oxopiperazines, which are further functionalized at C-3 via enolate formation and reaction with electrophiles. Notably, the two nitrogens of the ring can be orthogonally protected. (literal)
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- Autore CNR
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