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高效、简便、室温条件下的铑(I)阳离子催化的分子间[5+2]环加成反应:一步构建环庚烯及其文库。

Highly efficient, facile, room temperature intermolecular [5 + 2] cycloadditions catalyzed by cationic rhodium(I): one step to cycloheptenes and their libraries.

机构信息

Department of Chemistry, Stanford University, Stanford, California 94305-5080, USA.

出版信息

Org Lett. 2010 Apr 2;12(7):1604-7. doi: 10.1021/ol100337m.

Abstract

A cationic rhodium(I) complex--(C(10)H(8))Rh(cod) SbF(6)(-)--catalyzes the remarkably efficient intermolecular [5 + 2] cycloaddition of vinylcyclopropanes (VCPs) and various alkynes, providing cycloheptene cycloadducts in excellent yields in minutes at room temperature. The efficacy and selectivity of this catalyst are also shown in a novel diversification strategy, affording a cycloadduct library in one step from nine commercially available components.

摘要

一种阳离子铑(I)配合物--[(C(10)H(8))Rh(cod)]SbF(6)(-)--能够高效地催化乙烯基环丙烷(VCPs)与各种炔烃的[5 + 2]环加成反应,在室温下仅需几分钟即可得到高产率的环庚烯环加成产物。该催化剂还具有很好的效果和选择性,在一种新颖的多样化策略中,仅从九个市售原料一步即可得到一个环加成产物库。

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