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Shengbin Zhou

Researcher at Chinese Academy of Sciences

Publications -  45
Citations -  734

Shengbin Zhou is an academic researcher from Chinese Academy of Sciences. The author has contributed to research in topics: Enantioselective synthesis & Amino acid. The author has an hindex of 14, co-authored 41 publications receiving 653 citations. Previous affiliations of Shengbin Zhou include Stony Brook University.

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Ruthenium-Catalyzed Redox-Neutral [4 + 1] Annulation of Benzamides and Propargyl Alcohols via C–H Bond Activation

TL;DR: In this paper, the authors report ruthenium(II)-catalyzed redox-neutral annulation of benzamides and propargyl alcohols, in which propargy alcohols act as one-carbon units.
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Chemical kinetic resolution of unprotected β-substituted β-amino acids using recyclable chiral ligands.

TL;DR: The first chemical method for resolution of N,C-unprotected β-amino acids was developed through enantioselective formation and disassembly of nickel(II) complexes under operationally convenient conditions to prepare the anti-diabetic drug sitagliptin.
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Recyclable Ligands for the Non-Enzymatic Dynamic Kinetic Resolution of Challenging α-Amino Acids.

TL;DR: Structurally simple and inexpensive chiral tridentate ligands were employed for substantially advancing the purely chemical dynamic kinetic resolution of unprotected racemic tailor-made α-amino acids, enabling the first DKR of TM-α-AAs bearing tertiary alkyl chains as well as multiple unprotected functional groups.
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Asymmetric Synthesis of Sterically and Electronically Demanding Linear ω-Trifluoromethyl Containing Amino Acids via Alkylation of Chiral Equivalents of Nucleophilic Glycine and Alanine

TL;DR: An operationally convenient, scalable asymmetric synthesis of linear, ω-trifluoromethyl-containing amino acids, which were not previously produced in their enantiomerically pure form, has been developed via alkylation of chiral equivalents of nucleophilic glycine and alanine.