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Enantioselective Synthesis of Tertiary α,α-Diaryl Carbonyl Compounds Using Chiral N,N′-Dioxides under Umpolung Conditions
- Um, Tae-Woong;
- Lee, Girim;
- Shin, Seunghoon
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15초록
Bronsted acid-catalyzed addition of the chiral N,N'-dioxide into ynamides generated enolonium ions in situ which underwent enantioselective alkylation by indoles, pyrroles, and phenols, without racemization of the formed tertiary center. This external oxidant approach allows for the use of unmodified nucleophiles and does not leave trace groups from the oxidant, which significantly increases the synthetic efficiency and the product diversity. Furthermore, the byproduct of the N,N'-dioxide could be efficiently recycled into an optically pure form.
키워드
ALPHA-ARYLATION; CROSS-COUPLINGS; PALLADIUM; EFFICIENT; KETONES; SULFONIUM; LIGANDS
- 제목
- Enantioselective Synthesis of Tertiary α,α-Diaryl Carbonyl Compounds Using Chiral N,N′-Dioxides under Umpolung Conditions
- 저자
- Um, Tae-Woong; Lee, Girim; Shin, Seunghoon
- 발행일
- 2020-03
- 유형
- Article
- 저널명
- Organic Letters
- 권
- 22
- 호
- 5
- 페이지
- 1985 ~ 1990