Cu(OTf)<sub>2</sub>‐Catalyzed Selective Opening of Aryl and Vinyl Epoxides with Carbonyl Compounds to Give 1,3‐Dioxolanes.

Krasik, Pavel; Bohemier‐Bernard, Mathieu; Yu, Qing

doi:10.1002/chin.200531130

ChemInform

2005

DOI: 10.1002/chin.200531130

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Cu(OTf)₂‐Catalyzed Selective Opening of Aryl and Vinyl Epoxides with Carbonyl Compounds to Give 1,3‐Dioxolanes.

Pavel Krasik

Mathieu Bohemier‐Bernard

Qing Yu

Abstract: Give 1,3-Dioxolanes. -Epoxides are easily converted into the corresponding 1,3-dioxolanes by a selective and mild ring-opening reaction. -(KRASIK*, P.; BOHEMIER-BERNARD, M.; YU, Q.; Synlett 2005, 5, 854-856; Shire BioChem Inc., Laval, Que. H7V 4A7, Can.; Eng.) -C. Oppel 31-130

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Cu(OTf)₂‐Catalyzed Selective Opening of Aryl and Vinyl Epoxides with Carbonyl Compounds to Give 1,3‐Dioxolanes.

Abstract: Give 1,3-Dioxolanes. -Epoxides are easily converted into the corresponding 1,3-dioxolanes by a selective and mild ring-opening reaction. -(KRASIK*, P.; BOHEMIER-BERNARD, M.; YU, Q.; Synlett 2005, 5, 854-856; Shire BioChem Inc., Laval, Que. H7V 4A7, Can.; Eng.) -C. Oppel 31-130

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Cu(OTf)2‐Catalyzed Selective Opening of Aryl and Vinyl Epoxides with Carbonyl Compounds to Give 1,3‐Dioxolanes.

Abstract: Give 1,3-Dioxolanes. -Epoxides are easily converted into the corresponding 1,3-dioxolanes by a selective and mild ring-opening reaction. -(KRASIK*, P.; BOHEMIER-BERNARD, M.; YU, Q.; Synlett 2005, 5, 854-856; Shire BioChem Inc., Laval, Que. H7V 4A7, Can.; Eng.) -C. Oppel 31-130

Cited by 0 publications

References 1 publication

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Cu(OTf)₂‐Catalyzed Selective Opening of Aryl and Vinyl Epoxides with Carbonyl Compounds to Give 1,3‐Dioxolanes.