Cyclization Reaction for the Synthesis of Polysubstituted Naphthalenes in the Presence of Au(I) Precatalysts

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초록

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-COMPOUNDSLEWIS-ACIDSUBSTITUTED NAPHTHALENESREGIOSELECTIVE SYNTHESISINTRAMOLECULAR ADDITIONCLAISEN REARRANGEMENTMEDIATED CYCLIZATIONCATALYZED REACTIONSCARBONYL-COMPOUNDSMOLECULAR-OXYGEN
제목
Cyclization Reaction for the Synthesis of Polysubstituted Naphthalenes in the Presence of Au(I) Precatalysts
저자
Jagdale, Arun R.Park, Jong HyubYoun, So Won
DOI
10.1021/jo201339z
발행일
2011-09
유형
Article
저널명
Journal of Organic Chemistry
76
17
페이지
7204 ~ 7215