New boro amino amide organocatalysts for asymmetric cross aldol reaction of ketones with carbonyl compounds-Reference-Cited by-同舟云学术

New boro amino amide organocatalysts for asymmetric cross aldol reaction of ketones with carbonyl compounds

Published:2023 Issue:2 Volume:13 Page:888-894
ISSN:2046-2069
Container-title:RSC Advances
language:en
Short-container-title:RSC Adv.

Author:

Begum Zubeda¹,Seki Chigusa¹,Okuyama Yuko²,Kwon Eunsang³,Uwai Koji¹,Tokiwa Michio⁴,Tokiwa Suguru⁴,Takeshita Mitsuhiro⁴,Nakano Hiroto¹^ORCID

Affiliation:

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

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

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

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

Abstract

Distinct types of new boron fused primary amino amide organocatalysts were designed and synthesized from commercially available amino acids.

Publisher

Royal Society of Chemistry (RSC)

Subject

General Chemical Engineering,General Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2023/RA/D2RA06272K

Reference79 articles.

1. Novel Small Organic Molecules for a Highly Enantioselective Direct Aldol Reaction

2. Diphenylprolinol Methyl Ether: A Highly Enantioselective Catalyst for Michael Addition of Aldehydes to Simple Enones

3. Enantioselective Epoxidation of α,β-Enones Promoted by α,α-Diphenyl-l-prolinol as Bifunctional Organocatalyst

4. Small organic molecule catalyzed enantioselective direct aldol reaction in water

5. Organocatalytic Synthesis of Drugs and Bioactive Natural Products

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