Highly enantioselective one-pot sequential synthesis of valerolactones and pyrazolones bearing all-carbon quaternary stereocentres-Reference-Cited by-同舟云学术

Highly enantioselective one-pot sequential synthesis of valerolactones and pyrazolones bearing all-carbon quaternary stereocentres

Published:2021 Issue:7 Volume:19 Page:1610-1615
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Xu Yan-Li¹²³⁴⁵,Qin Zhou-Zhou¹²³⁴⁵,Wang Yu-Xia¹²³⁴⁵,Zhao Peng-Fei¹²³⁴⁵,Li Hong-Feng¹²³⁴⁵,Du Zhi-Hong¹²³⁴⁵,Da Chao-Shan¹²³⁴⁵^ORCID

Affiliation:

1. Institute of Biochemistry and Molecular Biology

2. School of Life Sciences

3. Lanzhou University

4. Lanzhou 730000

5. China

Abstract

Highly enantiopure and bioactive δ-valerolactones and pyrazolones, bearing α-all-carbon quaternary stereocentres, were successfully and sequentially prepared via a one-pot procedure catalysed by a new chiral squaramide under mild reaction conditions.

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2021/OB/D0OB02489A

Reference80 articles.

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2. Catalytic asymmetric synthesis of spirooxindoles: recent developments

3. Catalytic Enantioselective Construction of Spiro Quaternary Carbon Stereocenters

4. Progresses in organocatalytic asymmetric dearomatization reactions of indole derivatives

5. Acyclic Quaternary Carbon Stereocenters via Enantioselective Transition Metal Catalysis

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