Enantiopure 3,7-diazabicyclo[3.3.1]nonane derivatives 4 and 5, potential precursors of quinolizidine alkaloids, were synthesised in high yields, starting from the biocatalytic asymmetrization of sigma-symmetric 3,5-disubstituted piperidines. Their application to the total synthesis of the new pharmacologically active compounds 3 are also described. (C) 1999 Elsevier Science Ltd. All rights reserved.

An efficient chemoenzymatic access to chiral 3,7-diazabicyclo[3.3.1]nonane derivatives / B. Danieli, G. Lesma, D. Passarella, A. Silvani, N. Viviani. - In: TETRAHEDRON. - ISSN 0040-4020. - 55:40(1999), pp. 11871-11878. [10.1016/S0040-4020(99)00674-2]

An efficient chemoenzymatic access to chiral 3,7-diazabicyclo[3.3.1]nonane derivatives

B. Danieli
Primo
;
G. Lesma
Secondo
;
D. Passarella;A. Silvani
Penultimo
;
1999

Abstract

Enantiopure 3,7-diazabicyclo[3.3.1]nonane derivatives 4 and 5, potential precursors of quinolizidine alkaloids, were synthesised in high yields, starting from the biocatalytic asymmetrization of sigma-symmetric 3,5-disubstituted piperidines. Their application to the total synthesis of the new pharmacologically active compounds 3 are also described. (C) 1999 Elsevier Science Ltd. All rights reserved.
Alkaloids; Aminals; Bicyclic heterocyclic compounds; Enzyme reactions
Settore CHIM/06 - Chimica Organica
1999
Article (author)
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/177284
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