Stereoselective synthesis of β-proline derivatives from allylamines via domino hydroformylation/Wittig olefination and Aza-Michael addition
Under appropriate reaction conditions, a domino hydroformylation/Wittig olefination can be accomplished with derivatives of allylamines and stabilized Wittig ylides. A further highly diastereoselective aza-Michael reaction yields β-proline derivatives. These are, for example, useful as building bloc...
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| Main Authors: | , |
|---|---|
| Format: | Article (Journal) |
| Language: | English |
| Published: |
March 23, 2010
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| In: |
Advanced synthesis & catalysis
Year: 2010, Volume: 352, Issue: 6, Pages: 1023-1032 |
| ISSN: | 1615-4169 |
| DOI: | 10.1002/adsc.201000016 |
| Online Access: | Verlag, kostenfrei, Volltext: https://doi.org/10.1002/adsc.201000016 Verlag, kostenfrei, Volltext: https://onlinelibrary.wiley.com/doi/abs/10.1002/adsc.201000016 |
| Author Notes: | Andreas Farwick and Günter Helmchen |
MARC
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| 520 | |a Under appropriate reaction conditions, a domino hydroformylation/Wittig olefination can be accomplished with derivatives of allylamines and stabilized Wittig ylides. A further highly diastereoselective aza-Michael reaction yields β-proline derivatives. These are, for example, useful as building blocks for alkaloid syntheses. | ||
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