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Mukaiyama Aldol Reaction of 1,2-Bis(trimethylsiloxy) Cyclobutene Catalyzed by Magnesium(II) Iodide

Mukaiyama Aldol Reaction of 1,2-Bis(trimethylsiloxy) Cyclobutene Catalyzed by Magnesium(II) Iodide
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摘要 Efficient Mukaiyama-type aldol reaction of 1, 2-bis(trimethylsiloxy)cyclobutene with aromatic aldehydes catalyzed by MgI2 is reported. The resulting succinoylation product of aldehyde was converted into the synthetic useful g-lactone and butenolide derivatives. Efficient Mukaiyama-type aldol reaction of 1, 2-bis(trimethylsiloxy)cyclobutene with aromatic aldehydes catalyzed by MgI2 is reported. The resulting succinoylation product of aldehyde was converted into the synthetic useful g-lactone and butenolide derivatives.
出处 《Chinese Chemical Letters》 SCIE CAS CSCD 2003年第3期225-228,共4页 中国化学快报(英文版)
基金 We are grateful for the financial supports from the National Outstanding Youth Fund (No. 29925204) the Foundation for University Key Teacher by the Ministry of Education of China and a Visiting Fund of the National Laboratory of Applied Organic Chem
关键词 Mukaiyama aldol reaction 1 2-bis(trimethylsiloxy)cyclobutene magnesium iodide. Mukaiyama aldol reaction, 1, 2-bis(trimethylsiloxy)cyclobutene, magnesium iodide.
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参考文献3

  • 1E.Nakamura,I.Kuwajima,J.Am. Chemical Society Reviews . 1977
  • 2For examples.see reference3a and cited references6 to13; see also,X.Lin,R.W.Kavash,P.S.Mariano,J[].Journal of Organometallic Chemistry.1996
  • 3J.Shimada,K.Hashimoto,B.H.Kim,E.Nakamura,I.Kuwajima,J.Am. Chemical Society Reviews . 1984

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