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首页> 外文期刊>Angewandte Chemie >Organocatalytic Enantioselective Cascade Michael-Aldol Condensation Reactions: Efficient Assembly of Densely Functionalized Chiral Cyclopentenes
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Organocatalytic Enantioselective Cascade Michael-Aldol Condensation Reactions: Efficient Assembly of Densely Functionalized Chiral Cyclopentenes

机译:有机催化对映体级联迈克尔-奥尔多缩合反应:密集组装的手性环戊烯的高效组装。

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摘要

The development of asymmetric methods for the preparation of functionalized cyclopentenes has been of long-standing interest to organic chemists. As a result of their broad applications in organic synthesis they are widely distributed in a vast array of bioactive molecules. In the past, significant advances have been made in this area by using transition-metal-mediated [3+2] and [4+1] cycloaddition reactions. Furthermore, stereospecific ring opening of chiral cyclopro-panes, ring-closing metathesis of chiral dienes, and organ-ometallic-catalyzed Nazarov cyclizations have also been described.
机译:对于有机化学家来说,开发不对称方法来制备官能化环戊烯一直是人们的长期兴趣。由于它们在有机合成中的广泛应用,它们广泛分布在各种各样的生物活性分子中。过去,通过使用过渡金属介导的[3 + 2]和[4 + 1]环加成反应,该领域取得了重大进展。此外,还已经描述了手性环丙烷的立体特异性开环,手性二烯的闭环易位以及器官金属催化的Nazarov环化。

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