Catalytic Asymmetric Synthesis of Tertiary Alcohols and Oxetenes Bearing a Difluoromethyl Group

The catalytic asymmetric ene reaction with difluoropyruvate as an electrophile in the presence of a dicationic palladium complex is shown. This is the reliable and practical catalytic asymmetric synthesis for various α-CF2H tertiary alcohols in high yields and enantioselectivities. The reaction with...

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Veröffentlicht in:Organic letters 2015-10, Vol.17 (20), p.5108-5111
Hauptverfasser: Aikawa, Kohsuke, Yoshida, Seiya, Kondo, Daisuke, Asai, Yuya, Mikami, Koichi
Format: Artikel
Sprache:eng
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Zusammenfassung:The catalytic asymmetric ene reaction with difluoropyruvate as an electrophile in the presence of a dicationic palladium complex is shown. This is the reliable and practical catalytic asymmetric synthesis for various α-CF2H tertiary alcohols in high yields and enantioselectivities. The reaction with isobutene can be catalyzed efficiently under solvent-free conditions with low catalyst loading (up to S/C 2000). Furthermore, difluoropyruvate is applicable to the [2 + 2] cycloaddition reaction in high yields and enantioselectivities.
ISSN:1523-7060
1523-7052
DOI:10.1021/acs.orglett.5b02617