http://www.cnr.it/ontology/cnr/individuo/prodotto/ID19846
Terminal oxazolinyloxiranes: synthesis, reaction with amines and regioselective b-lithiation (Articolo in rivista)
- Type
- Label
- Terminal oxazolinyloxiranes: synthesis, reaction with amines and regioselective b-lithiation (Articolo in rivista) (literal)
- Anno
- 2009-01-01T00:00:00+01:00 (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
- 10.1016/j.tet.2009.08.040 (literal)
- Alternative label
Degennaro L.; Capriati V.; Carlucci C.; Florio S.; Luisi R.; Nuzzo I.; Cuocci C. (2009)
Terminal oxazolinyloxiranes: synthesis, reaction with amines and regioselective b-lithiation
in Tetrahedron (Oxf., Print)
(literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
- Degennaro L.; Capriati V.; Carlucci C.; Florio S.; Luisi R.; Nuzzo I.; Cuocci C. (literal)
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- Rivista
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- Note
- ISI Web of Science (WOS) (literal)
- Scopu (literal)
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- Dipartimento Farmaco-Chimico, Universita degli Studi di Bari and Consorzio Interuniversitario Nazionale CINMPIS, Via E. Orabona 4, 70125 Bari, Italy
Istituto di Cristallografia (IC-CNR), Via Amendola 122/o, 70126 Bari, Italy (literal)
- Titolo
- Terminal oxazolinyloxiranes: synthesis, reaction with amines and regioselective b-lithiation (literal)
- Abstract
- The synthesis of terminal oxazolinyloxiranes, even in enantioenriched form, has been performed by Darzens-type reaction of lithiated chloroalkyloxazolines with benzotriazolylmethanol (BtCH(2)OH) or by chloromethylation of 2-acyl-2-oxazolines. The synthetic utility of such oxiranes based on their ability to act either as electrophiles, undergoing ring-opening reactions with nucleophiles, or as nucleophiles in form of the oxiranyl anions, generated by stereoselective beta-deprotonation, has been investigated. (C) 2009 Elsevier Ltd. All rights reserved (literal)
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- Autore CNR
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