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手性镍(II)配合物催化的直接和对映选择性羟醛反应。

Direct and Enantioselective Aldol Reactions Catalyzed by Chiral Nickel(II) Complexes.

作者信息

Kennington Stuart C D, Teloxa Saul F, Mellado-Hidalgo Miguel, Galeote Oriol, Puddu Sabrina, Bellido Marina, Romea Pedro, Urpí Fèlix, Aullón Gabriel, Font-Bardia Mercè

机构信息

Department of Inorganic and Organic Chemistry, Section of Organic Chemistry, Universitat de Barcelona, Carrer Martí i Franqués 1-11, 08028, Barcelona, Spain.

Department of Inorganic and Organic Chemistry, Section of Inorganic Chemistry, Universitat de Barcelona, Carrer Martí i Franqués 1-11, 08028, Barcelona, Spain.

出版信息

Angew Chem Int Ed Engl. 2021 Jul 5;60(28):15307-15312. doi: 10.1002/anie.202104352. Epub 2021 Jun 7.

Abstract

A direct and asymmetric aldol reaction of N-acyl thiazinanethiones with aromatic aldehydes catalyzed by chiral nickel(II) complexes is reported. The reaction gives the corresponding O-TIPS-protected anti-aldol adducts in high yields and with remarkable stereocontrol and atom economy. Furthermore, the straightforward removal of the achiral scaffold provides enantiomerically pure intermediates of synthetic interest, which involve precursors for anti-α-amino-β-hydroxy and α,β-dihydroxy carboxylic derivatives. Theoretical calculations explain the observed high stereocontrol.

摘要

报道了在手性镍(II)配合物催化下,N-酰基硫代噻嗪酮与芳香醛的直接不对称羟醛反应。该反应以高产率、显著的立体控制和原子经济性得到相应的O-TIPS保护的反式羟醛加合物。此外,非手性骨架的直接去除提供了具有合成价值的对映体纯中间体,其中包括抗α-氨基-β-羟基和α,β-二羟基羧酸衍生物的前体。理论计算解释了观察到的高立体控制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eecc/8362213/bd53b77fd6e8/ANIE-60-15307-g003.jpg

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