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Stereoselective aza...
Stereoselective aza-Diels-Alder reactions with 2H-azirines as dienophiles furnishing highly functionalized tetrahydropyridines
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Timen, A. S. (författare)
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- Fischer, Andreas (författare)
- KTH,Kemi
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- Somfai, Peter (författare)
- KTH,Kemi
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(creator_code:org_t)
- Royal Society of Chemistry (RSC), 2003
- 2003
- Engelska.
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Ingår i: Chemical Communications. - : Royal Society of Chemistry (RSC). - 1359-7345 .- 1364-548X. ; :10, s. 1150-1151
- Relaterad länk:
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https://urn.kb.se/re...
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https://doi.org/10.1...
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Abstract
Ämnesord
Stäng
- Highly diastereoselective Lewis acid mediated aza-Diels-Alder reactions of chiral auxiliary derivatized 2H-azirines have been accomplished for the first time, yielding bi and tricyclic heterocyclic compounds, comprising aziridine and tetrahydropyridine substructures, in up to 97% de; with the absolute stereochemistry of the major product confirmed by X-ray crystallography.
Nyckelord
- diastereoselective synthesis
- cycloadditions
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- ref (ämneskategori)
- art (ämneskategori)
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