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An Efficient Synthesis of Trihydroxy Quinolizidine Alkaloids Using Ring-Closing Metathesis
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.
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Published in: | Synlett 2004-07, Vol.2004 (9), p.1549-1552 |
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Main Authors: | , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that cite this one |
Online Access: | Get full text |
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Summary: | 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. |
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ISSN: | 0936-5214 1437-2096 |
DOI: | 10.1055/s-2004-829538 |