Regio- and stereoselective nucleophilic addition reactions of Swaminathan ketone and its methylated analog using organometallic reagents
[Display omitted] Herein, we report the regio- and stereoselective nucleophilic addition reactions of Swaminathan ketone 2a and its methylated analog 2b, both of which contain a 6–7 fused carbocyclic enedione moiety. Nucleophilic additions to 2 using generic organometallic reagents, such as Grignard...
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Veröffentlicht in: | Tetrahedron letters 2023-11, Vol.132, p.154800, Article 154800 |
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Format: | Artikel |
Sprache: | eng |
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