Chiral sulfoxides: advances in asymmetric synthesis and problems with the accurate determination of the stereochemical outcome-Reference-Cited by-全球学者库

Chiral sulfoxides: advances in asymmetric synthesis and problems with the accurate determination of the stereochemical outcome

Published:2018 Issue:4 Volume:47 Page:1307-1350
ISSN:0306-0012
Container-title:Chemical Society Reviews
language:en
Short-container-title:Chem. Soc. Rev.

Author:

Han Jianlin¹²³⁴⁵^ORCID,Soloshonok Vadim A.⁶⁷⁸⁹¹⁰^ORCID,Klika Karel D.¹¹¹²¹³¹⁴^ORCID,Drabowicz Józef¹⁵¹⁶¹⁷¹⁸¹⁹^ORCID,Wzorek Alicja⁶⁷⁸⁹¹⁰^ORCID

Affiliation:

1. School of Chemistry and Chemical Engineering

2. State Key Laboratory of Coordination Chemistry

3. Jiangsu Key Laboratory of Advanced Organic Materials

4. Nanjing University

5. 210093 Nanjing

6. Department of Organic Chemistry I

7. Faculty of Chemistry

8. University of the Basque Country UPV/EHU

9. 20018 San Sebastián

10. Spain

11. Molecular Structure Analysis

12. German Cancer Research Center (DKFZ)

13. D-69009 Heidelberg

14. Germany

15. Department of Heterooganic Chemistry

16. Center of Molecular and Macromolecular Studies

17. Polish Academy of Sciences

18. 90-363 Łódź

19. Poland

Abstract

This review covers recent developments for optically active sulfoxide preparations and the problem of accurate determination of the stereochemical outcome due to the self-disproportionation of enantiomers (SDE).

Funder

National Natural Science Foundation of China

Narodowe Centrum Nauki

Ministerstwo Nauki i Szkolnictwa Wyższego

Ikerbasque, Basque Foundation for Science

Publisher

Royal Society of Chemistry (RSC)

Subject

General Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2018/CS/C6CS00703A

Reference231 articles.

1. Use of chiral sulfoxides in asymmetric synthesis

2. Recent Developments in the Synthesis and Utilization of Chiral Sulfoxides

3. Applications of Sulfoxides to Asymmetric Synthesis of Biologically Active Compounds

4. CCLXXIX.—The dependence of rotatory power on chemical constitution. Part XXIX. The resolution of sulphoxides into their optically active forms

5. THE REACTION BETWEEN ORGANOMAGNESIUM HALIDES AND THE ESTERS OF SOME SULFUR ACIDS

Cited by 195 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. Engineering of methionine sulfoxide reductase A with simultaneously improved stability and activity for kinetic resolution of chiral sulfoxides;International Journal of Biological Macromolecules;2024-03

2. Synthesis of β‐Amino Acid Derivatives via Enantioselective Lewis Base Catalyzed N‐Allylation of Halogenated Amides with Morita‐Baylis‐Hillman Carbonates;Chemistry – A European Journal;2024-01-16

3. Altering the mobile phase composition to enhance self-disproportionation of enantiomers in achiral chromatography;Journal of Chromatography A;2024-01

4. Nickel‐Catalyzed Enantioselective Synthesis of Dienyl Sulfoxide;Angewandte Chemie;2023-12-27

5. Nickel‐Catalyzed Enantioselective Synthesis of Dienyl Sulfoxide;Angewandte Chemie International Edition;2023-12-27