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Synthesis of the tricyclic core structure of vindoline
Graphic An efficient synthesis of the core tricyclic structure ( 18 ) of vindoline has been achieved using the strategy, which features an intramolecular 1,3-dipolar cycloaddition of the azido dienone ( 12 ) to give aziridine ( 13 ) with complete region- and stereocontrol.
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Published in: | Tetrahedron letters 2004-01, Vol.45 (5), p.919-921 |
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Main Authors: | , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Graphic
An efficient synthesis of the core tricyclic structure (
18
) of vindoline has been achieved using the strategy, which features an intramolecular 1,3-dipolar cycloaddition of the azido dienone (
12
) to give aziridine (
13
) with complete region- and stereocontrol. |
---|---|
ISSN: | 0040-4039 1873-3581 |
DOI: | 10.1016/j.tetlet.2003.11.115 |