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Phosphoramidite Gold(I)-Catalyzed Diastereo- and Enantioselective Synthesis of 3,4-Substituted Pyrrolidines

机译:亚磷酰胺金(I)催化的3,4-取代吡咯烷的非对映和对映选择性合成

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摘要

In this article the utility of phosphoramidite ligands in enantioselective AuI catalysis was explored in the development of highly diastereo- and enantioselective AuI-catalyzed cycloadditions of allenenes. A Au^I-catalyzed synthesis of 3,4-disubstituted pyrrolidines and γ-lactams is described. This reaction proceeds through the enantioselective AuI-catalyzed cyclization of allenenes to form a carbocationic intermediate that is trapped by an exogenous nucleophile, resulting in the highly diastereoselective construction of three contiguous stereogenic centers. A computational study (DFT) was also performed to gain some insight into the underlying mechanisms of these cycloadditions. The utility of this new methodology was demonstrated through the formal synthesis of (−)-isocynometrine.udud
机译:在本文中,亚磷酰胺配体在对映选择性AuI催化中开发了高度非对映和对映选择性AuI催化的丙二烯环加成反应。描述了Au ^ I催化的3,4-二取代的吡咯烷和γ-内酰胺的合成。该反应通过对映异构体的对映选择性AuI催化的环化反应进行,形成碳阳离子中间物,该中间物被外源性亲核试剂捕获,导致三个连续的立体中心高度非对映选择性。还进行了计算研究(DFT),以深入了解这些环加成的潜在机理。通过(-)-异氰尿素的正式合成证明了这种新方法的效用。 ud ud

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