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有机催化的环丁酮不对称共轭加成:[6,5,4]-稠合碳环的对映选择性和非对映选择性合成。

Organocatalytic Desymmetric Conjugate Addition to Cyclobutanone: An Enantio- and Diastereoselective Synthesis of [6,5,4]-Fused Carbocycles.

机构信息

Department of Chemistry, Indian Institute of Science Education and Research (IISER) Bhopal, Bhopal By-pass Road, Bhauri, Bhopal, 462066, India.

出版信息

Chemistry. 2023 Apr 25;29(24):e202203407. doi: 10.1002/chem.202203407. Epub 2023 Mar 17.

Abstract

The first organocatalytic, non-destructive desymmetrisation of 3-substituted cyclobutanone followed by intramolecular cyclisation is described. Owing to the slow activation of the pronucleophile by the weak Brønsted base, the α-functionalization of ketones with tertiary-amine-derived Brønsted base catalysis has been chemically challenging in asymmetric transformations. Herein, we demonstrate that the cinchona-derived squaramide catalyst works effectively for the intramolecular Michael addition of cyclobutanone to enones and affords the architecturally fascinating [6,5,4]-fused carbocyclic skeleton in good yields and excellent diastereo- and enantioselectivities (up to >20 : 1 dr and 96 % ee). Furthermore, as a synthetic application, this method provides an alternative pathway to enantioenriched high-value products like γ-lactones and indan-2-ol derivatives.

摘要

首次报道了 3-取代环丁酮的首例有机催化、非破坏性去对称化,随后进行分子内环化。由于弱布朗斯特碱对亲核试剂的缓慢活化,酮的α-功能化在不对称转化中具有叔胺衍生的布朗斯特碱催化作用具有化学挑战性。在此,我们证明,金鸡纳衍生的螺二酰胺催化剂在环丁酮与烯酮的分子内迈克尔加成中能有效地发挥作用,并以良好的收率和优异的非对映选择性和对映选择性(高达>20:1 dr 和 96%ee)得到结构引人入胜的[6,5,4]-稠合碳环骨架。此外,作为一种合成应用,该方法为手性富集的高附加值产物(如γ-内酰胺和茚满-2-醇衍生物)提供了另一种途径。

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