Enantioselective synthesis of α,α-difluoro-β-lactams using amino alcohol ligands

Author:

Tarui Atsushi123,Ikebata Takeshi123,Sato Kazuyuki123,Omote Masaaki123,Ando Akira123

Affiliation:

1. Faculty of Pharmaceutical Sciences

2. Setsunan University

3. Hirakata, Japan

Abstract

A practical and highly enantioselective Reformatsky reaction of ethyl bromodifluoroacetate with imines using a cheap and commercially available amino alcohol ligand is described.

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Cited by 21 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. Zinc Enolates: The Reformatsky and Blaise Reactions;Reference Module in Chemistry, Molecular Sciences and Chemical Engineering;2023

2. Azetidines, Azetines and Azetes: Monocyclic;Comprehensive Heterocyclic Chemistry IV;2022

3. The Asymmetric Difluoro‐Reformatsky Reaction;European Journal of Organic Chemistry;2021-02-19

4. Copper-catalyzed [3 + 1] cyclization of cyclopropenes/diazo compounds and bromodifluoroacetamides: facile synthesis of α,α-difluoro-β-lactam derivatives;Chemical Science;2021

5. Stereoselective Synthesis of Multisubstituted α-fluoro-β-lactams;Current Organic Chemistry;2020-11-18

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