STEREOSELECTIVE ROUTE TO HIGHLY FUNCTIONALIZED AMINO-ALCOHOLS
| Data(s) |
10/06/1991
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|---|---|
| Resumo |
<p>Acyclic amino alcohols can be obtained in high stereoisomeric purity by Stevens [2,3] rearrangement of tetrahydropyridine salts followed by reduction of the ketones and ring opening of the disubstituted pyrrolidine.</p> |
| Identificador | |
| Idioma(s) |
eng |
| Direitos |
info:eu-repo/semantics/restrictedAccess |
| Fonte |
COATES , B , MALONE , J F , MCCARNEY , M T , STEVENSON , P J & Stevenson , P 1991 , ' STEREOSELECTIVE ROUTE TO HIGHLY FUNCTIONALIZED AMINO-ALCOHOLS ' Tetrahedron Letters , vol 32 , no. 24 , pp. 2827-2828 . |
| Palavras-Chave | #[2,3] SIGMATROPIC REARRANGEMENT #AMINO KETONE #AMINO ALCOHOL #CHELATION CONTROLLED REDUCTION |
| Tipo |
article |
