AI Article Synopsis
- A new reaction method was created to synthesize highly substituted indolizines by reacting pyrrole-2-carbaldehyde derivatives with o-hydroxyphenyl propargylamines using a base-promoted oxidative process.
- This method utilizes DBN as the base and can produce a variety of 5,6,7-trisubstituted indolizines effectively.
- The synthesis is efficient, achieving good to excellent yields while accommodating many useful functional groups under mild conditions.
Article Abstract
A base promoted oxidative [4+2] annulation of pyrrole-2-carbaldehyde derivatives with o-hydroxyphenyl propargylamines for the synthesis of highly substituted indolizines has been developed. Using DBN as base, a broad range of 5,6,7-trisubstituted indolizines have been prepared in good to excellent yields under mild conditions, and many useful functional groups can be tolerated.
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| http://dx.doi.org/10.1002/chem.202402487 | DOI Listing |
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