The sequential C- and N-allylation of D-glucose-derived nitrone 2 provides the required diene functionality with nitrogen linker that was used in ring-closing metathesis pathway in the synthesis of quinolizidine alkaloids 1a and 1b.
D. D. Dhavale, S. M. Jachak, N. P. Karche, C. Trombini (2004). An efficient synthesis of trihydroxy quinolizidine alkaloids using ring-closing metathesis. SYNLETT, -, 1549-1552 [10.1055/s-2004-829538].
An efficient synthesis of trihydroxy quinolizidine alkaloids using ring-closing metathesis
TROMBINI, CLAUDIO
2004
Abstract
The sequential C- and N-allylation of D-glucose-derived nitrone 2 provides the required diene functionality with nitrogen linker that was used in ring-closing metathesis pathway in the synthesis of quinolizidine alkaloids 1a and 1b.File in questo prodotto:
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