Organocatalytic Asymmetric Domino Oxa-Michael–Mannich-[1,3]-Amino Rearrangement Reaction of N-Tosylsalicylimines to α,β-Unsaturated Aldehydes by Diarylprolinol Silyl Ethers-Reference-Cited by-同舟云学术

Organocatalytic Asymmetric Domino Oxa-Michael–Mannich-[1,3]-Amino Rearrangement Reaction of N-Tosylsalicylimines to α,β-Unsaturated Aldehydes by Diarylprolinol Silyl Ethers

Published:2019-12-12 Issue:6 Volume:85 Page:4011-4018
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Hu Sha¹,Wang Jiaqi¹,Huang Guanxin¹,Zhu Kejie¹,Chen Fener¹²^ORCID

Affiliation:

1. Department of Chemistry, Fudan University, Shanghai 200433, China

2. Institute of Pharmaceutical Science and Technology, Zhejiang University of Technology, 18 Chao Wang Road, Hangzhou 310014, China

Funder

Shanghai Municipality

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.joc.9b02939

Reference48 articles.

1. Enantioselective Organocatalyzed α Sulfenylation of Aldehydes

2. Diphenylprolinol Silyl Ethers as Efficient Organocatalysts for the Asymmetric Michael Reaction of Aldehydes and Nitroalkenes

3. Diarylprolinol Ethers: Expanding the Potential of Enamine/Iminium-Ion Catalysis

4. Highly Efficient Asymmetric Michael Reaction of Aldehydes to Nitroalkenes with Diphenylperhydroindolinol Silyl Ethers as Organocatalysts

5. Organocatalytic, Enantioselective Intramolecular [6 + 2] Cycloaddition Reaction for the Formation of Tricyclopentanoids and Insight on Its Mechanism from a Computational Study

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