Literature DB >> 33226708

Copper(I)-Catalyzed Asymmetric Interrupted Kinugasa Reaction: Synthesis of α-Thiofunctional Chiral β-Lactams.

Jialin Qi1, Fang Wei1, Shuai Huang1, Chen-Ho Tung1, Zhenghu Xu1,2.   

Abstract

A copper(I)-catalyzed asymmetric, three-component interrupted Kinugasa reaction has been developed. Diverse chiral sulfur-containing chiral β-lactams with two consecutive stereogenic centers were synthesized in one step from readily available starting materials in good yields and with excellent diastereo- and enantioselectivity. The key is the interception of in situ formed chiral four membered copper(I) enolate intermediate with sulfur electrophiles.
© 2020 Wiley-VCH GmbH.

Entities:  

Keywords:  Kinugasa reaction; asymmetric catalysis; copper; sulfur; β-lactams

Year:  2021        PMID: 33226708     DOI: 10.1002/anie.202013450

Source DB:  PubMed          Journal:  Angew Chem Int Ed Engl        ISSN: 1433-7851            Impact factor:   15.336


  2 in total

1.  Copper(i)-catalyzed radical carboamination reaction of 8-aminoquinoline-oriented buteneamides with chloroform: synthesis of-β-lactams.

Authors:  Zixu Gan; Ke Zhang; Peng Shi; Yingsheng Zhao; Runsheng Zeng
Journal:  RSC Adv       Date:  2021-08-19       Impact factor: 4.036

2.  Enantioselective [1,2]-Stevens rearrangement of thiosulfonates to construct dithio-substituted quaternary carbon centers.

Authors:  Linfeng Hu; Jinzhao Li; Yongyan Zhang; Xiaoming Feng; Xiaohua Liu
Journal:  Chem Sci       Date:  2022-03-11       Impact factor: 9.825

  2 in total

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