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Cyclization Reaction for the Synthesis of Polysubstituted Naphthalenes in the Presence of Au(I) Precatalysts
- Jagdale, Arun R.;
- Park, Jong Hyub;
- Youn, So Won
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56초록
Au(I)-catalyzed cyclization of alkenyl carbonyl compounds leading to a variety of substituted naphthalenes has been developed. This process exploits a dual function of the Au(I) catalyst: (1) the oxophilic nature of the Au(I) catalyst, counterintuitive to the pi-acidic reactivities generally associated with Au catalysts, and (2) olefin isomerization supported by the outcome of isotope scrambling experiments. It cannot be completely excluded that TfOH is a true operative catalyst in this protocol. In view of the practicality, the unnecessity of isomerically pure starting material in this reaction is particularly attractive and valuable.
키워드
ACTIVATED METHYLENE-COMPOUNDS; LEWIS-ACID; SUBSTITUTED NAPHTHALENES; REGIOSELECTIVE SYNTHESIS; INTRAMOLECULAR ADDITION; CLAISEN REARRANGEMENT; MEDIATED CYCLIZATION; CATALYZED REACTIONS; CARBONYL-COMPOUNDS; MOLECULAR-OXYGEN
- 제목
- Cyclization Reaction for the Synthesis of Polysubstituted Naphthalenes in the Presence of Au(I) Precatalysts
- 저자
- Jagdale, Arun R.; Park, Jong Hyub; Youn, So Won
- 발행일
- 2011-09
- 유형
- Article
- 권
- 76
- 호
- 17
- 페이지
- 7204 ~ 7215