(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.
(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]
(1S,2S)-1-Amino-2-hydroxy-1,2,3,4-tetrahydronaphthalene: a new chiral auxiliary for asymmetric reformatsky reactions
F. OrsiniPrimo
;G. SelloSecondo
;A.M. ManzoPenultimo
;E.M. LucciUltimo
2005
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.
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