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Volumn 133, Issue 16, 2011, Pages 6187-6193

Palladium-catalyzed cycloisomerizations of (Z)-1-iodo-1,6-dienes: Iodine atom transfer and mechanistic insight to alkyl iodide reductive elimination

Author keywords

[No Author keywords available]

Indexed keywords

A-CARBON; ALKENE INSERTION; ALKYL IODIDES; CATALYTIC CYCLES; CONTROL EXPERIMENTS; CYCLOISOMERIZATIONS; FACILE METHOD; FERROCENES; FURTHER DEVELOPMENT; HETEROCYCLES; IODINE ATOMS; OPTIMAL CHOICE; OXIDATIVE ADDITIONS; REDUCTIVE ELIMINATION; STEREOSPECIFIC; TRANSFER PROCESS; VINYL IODIDES;

EID: 79954988580     PISSN: 00027863     EISSN: 15205126     Source Type: Journal    
DOI: 10.1021/ja201204g     Document Type: Article
Times cited : (139)

References (87)
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    • Actually, 5% of byproduct 6 was isolated along with 2j in the case of 1j. Compound 2j can be transformed into 6 under either the optimized conditions or the classical radical reaction conditions, indicating that the catalyst (palladium + DPPF) might also promote a radical process
    • Actually, 5% of byproduct 6 was isolated along with 2j in the case of 1j. Compound 2j can be transformed into 6 under either the optimized conditions or the classical radical reaction conditions, indicating that the catalyst (palladium + DPPF) might also promote a radical process.


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