(1S,2S)-1-Amino-2-hydroxy-1,2,3,4-tetrahydronaphthalene: a new chiral auxiliary for asymmetric reformatsky reactions
Articolo
Data di Pubblicazione:
2005
Citazione:
(1S,2S)-1-Amino-2-hydroxy-1,2,3,4-tetrahydronaphthalene: a new chiral auxiliary for asymmetric reformatsky reactions / F. Orsini, G. Sello, A.M. Manzo, E.M. Lucci. - In: TETRAHEDRON-ASYMMETRY. - ISSN 0957-4166. - 16:11(2005 Jun 06), pp. 1913-1918. [10.1016/j.tetasy.2005.04.008]
Abstract:
(1S,2S)-1-Amino-2-hydroxy-1,2,3,4-tetrahydronapthanlene, synthesized via a chemoenzymatic approach from naphthalene, has been successfully used as a chiral auxiliary in Reformatsky-type reactions between the corresponding alpha-bromoacyloxazolidinone and carbonyl compounds.
Tipologia IRIS:
01 - Articolo su periodico
Keywords:
cobalt-phosphine complex; enolate aldol reaction; acylation reactions; addition-reactions; anti-aldols; N-acylation; derivates; alpha; acids; cis-1-arylsulfonamido-2-indanols
Elenco autori:
F. Orsini, G. Sello, A.M. Manzo, E.M. Lucci
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