Asymmetric Catalytic [2,3] Stevens and Sommelet–Hauser Rearrangements of α‐Diazo Pyrazoleamides with Sulfides-Reference-Cited by-同舟云学术

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Asymmetric Catalytic [2,3] Stevens and Sommelet–Hauser Rearrangements of α‐Diazo Pyrazoleamides with Sulfides

Published:2019-09-16 Issue:38 Volume:58 Page:13492-13498
ISSN:1433-7851
Container-title:Angewandte Chemie International Edition
language:en
Short-container-title:Angew. Chem. Int. Ed.

Author:

Lin Xiaobin¹^ORCID,Yang Wei¹,Yang Wenkun¹,Liu Xiaohua¹^ORCID,Feng Xiaoming¹^ORCID

Affiliation:

1. Key Laboratory of Green Chemistry & TechnologyMinistry of EducationCollege of ChemistrySichuan University Chengdu 610064 China

Funder

National Natural Science Foundation of China

Graduate Student's Research and Innovation Fund of Sichuan University

Publisher

Wiley

Subject

General Chemistry,Catalysis

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/anie.201907164

Reference79 articles.

1. For selected examples of chiral sulfoxides as efficient ligands see:

2. C–H to C–N Cross-Coupling of Sulfonamides with Olefins

3. Copper-Catalyzed Enantioselective 1,6-Boration ofpara-Quinone Methides and Efficient Transformation ofgem-Diarylmethine Boronates to Triarylmethanes

4. Copper-Catalyzed Enantioselective 1,6-Boration ofpara-Quinone Methides and Efficient Transformation ofgem-Diarylmethine Boronates to Triarylmethanes

5. For selected examples of optically active sulfur-containing pharmaceuticals see:

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