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氨基醇砌块用于螺/环丙环类手性化合物的合成
引用本文:王建平,陈庆华. 氨基醇砌块用于螺/环丙环类手性化合物的合成[J]. 有机化学, 2001, 21(10): 728-731
作者姓名:王建平  陈庆华
作者单位:1. 洛阳师范学院化学系,
2. 北京师范大学化学系,
基金项目:国家自然科学基金资助课题(№.29672004).
摘    要:手性氨基醇砌块3与5-(l-孟氧基)-3-溴-2(5H)-呋喃酮手性合成子4通过串联的不对称双Michael加成/分子内亲核取代反应,得到了具有四个新的手性中心的氨基醇手性砌块/螺环/环丙烷类化合物7(44%~57%,de≥98%)。通过元素分析,[α]^20~D,UV,IR,^1HNMR,^13CNMR,MS确认了它们的化学结构。本工作可以为含有某些活性官能团的多手性中心的复杂结构化合物提供新的合成策略。

关 键 词:氨基醇P  不对称反应  迈克尔加成反应  亲核反应  砌块  螺环化合物  环丙烷P  手性试剂  合成
修稿时间:2001-01-08

Application of amino alcohol as chiral building block in synthesis of spiro-cyclopropane derivatives containing multiple stereogenic centers
Affiliation:Beijing Normal Univ., Dept of Chem..Beijing(100875)
Abstract:The unusual, functionalized spiro-cyclopropane derivatives 7 containing four stereogenic centers were obtained in good yields with de≥98% via tandem double Michael addition/internal nucleophilic substitution of the chiral synthon, 5-l-menthyloxy-3-bromo-2-(5H)- furanone(4), with amino alcohol as chiral building block 3 under mild conditions. The novel chiral compounds 7 were identified on the basis of their analytcal data and spectroscopic data, such as UV, IR, ^1H NMR, ^13C NMR, MS and elementary analysis. This result can provide importnat synthetic strategy in synthesis of some complex molecules containing spiro-cyclopropane skeleton with multiple chiral centers.
Keywords:AMINO ALCOHOL P  MICHAEL ADDITION REACTION  NUCLEOPHILIC REACTION  BLOCK  SPIRO COMPOUNDS  CYCLOPROPANE P  CHIRAL REAGENT  SYNTHESIS
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