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Volumn 62, Issue 9, 1997, Pages 2968-2974

Lewis Acid Promoted [2 + 1] Cycloaddition Reactions of 1-Seleno-2-silylethene with Tricarbonyl-Substituted Olefins

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EID: 0001525655     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo9622486     Document Type: Article
Times cited : (33)

References (69)
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    • 4 gave a small amount of desilylated adduct as a mixture with recovered 6, and 68% of 1a was recovered. The cyclopropane, possibly produced in low yield, could be unstable to these reaction conditions.
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    • 13C NMR spectra of an authentic sample 20 were kindly provided by Sumitomo Chemical Co., Ltd. 2-1, Takatsukasa 4-chome, Takarazuka, Hyogo 665, Japan.
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    • 2.
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    • note
    • 5 On the other hand, the mechanism in Scheme 4 cannot explain the selectivity of three-membered-ring and four-membered-ring formations. A detailed investigation of the intermediacy of Y and Z in this system is now underway. We appreciate the suggestion of the reviewer on the possibility of this alternative mechanism.


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