Amino Amide Organocatalysts for Asymmetric Michael Addition of β-Keto Esters with β-Nitroolefins-Reference-Cited by-同舟云学术

Amino Amide Organocatalysts for Asymmetric Michael Addition of β-Keto Esters with β-Nitroolefins

Published:2019-03-15 Issue:3 Volume:92 Page:696-701
ISSN:0009-2673
Container-title:Bulletin of the Chemical Society of Japan
language:en
Short-container-title:BCSJ

Author:

Owolabi Isiaka Alade¹,Chennapuram Madhu¹,Seki Chigusa¹,Okuyama Yuko²,Kwon Eunsang³,Uwai Koji¹,Tokiwa Michio⁴,Takeshita Mitsuhiro⁴,Nakano Hiroto¹

Affiliation:

1. Division of Sustainable and Environmental Engineering, Graduate School of Engineering, Muroran Institute of Technology, 27-1 Mizumoto, Muroran, Hokkaido 050-8585, Japan

2. Tohoku Medical and Pharmaceutical University, 4-4-1 Komatsushima, Aoba-ku, Sendai, Miyagi 981-8558, Japan

3. Research and Analytical Center for Giant Molecules, Graduate School of Sciences, Tohoku University, 6-3 Aoba, Aramaki, Aoba-ku, Sendai, Miyagi 980-8578, Japan

4. Tokiwakai Group, 62 Numajiri, Tsuduri-chou, Uchigo, Iwaki, Fukushima 973-8053, Japan

Publisher

The Chemical Society of Japan

Subject

General Chemistry

Link

http://www.journal.csj.jp/doi/pdf/10.1246/bcsj.20180302

Reference95 articles.

1. Thia-Michael Addition: An Emerging Strategy in Organic Synthesis

2. Asymmetric Michael Reaction of Aldehyde and β-Substituted α-Nitroacrylate Catalyzed by Diphenylprolinol Silyl Ether

3. Allenedicarboxylate as a Stereochemically Labile Electrophile for Chiral Organic Base-catalyzed Stereoselective Michael Addition

4. Chiral 2-Aminobenzimidazoles in Deep Eutectic Mixtures: Recyclable Organocatalysts for the Enantioselective Michael Addition of 1,3-Dicarbonyl Compounds to β-Nitroalkenes

5. Catalytic Asymmetric Conjugate Addition of Indolizines to α,β-Unsaturated Ketones

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