金鸡纳
烯醇
硅烷化
硅烷
对映选择合成
催化作用
化学
有机化学
芳基
烷基
硅烷
作者
Takehisa Ishimaru,Norio Shibata,Takao Horikawa,Naomi Yasuda,Shuichi Nakamura,Takeshi Toru,Motoo Shiro
标识
DOI:10.1002/anie.200800717
摘要
Catalytic variant: Allyl silanes and silyl enol ethers 1 are good substrates for the catalytic highly enantioselective fluorodesilylation using a combination of a bis-cinchona alkaloid, N-fluorobenzenesulfonimide (NFSI), and base (see scheme). Pharmaceutically attractive 3-aryl-3-fluorooxindoles such as 3 can also be synthesized with high enantioselectivity. Supporting information for this article is available on the WWW under http://www.wiley-vch.de/contents/jc_2002/2008/z800717_s.pdf or from the author. Please note: The publisher is not responsible for the content or functionality of any supporting information supplied by the authors. Any queries (other than missing content) should be directed to the corresponding author for the article.
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