Highly efficient organocatalysts for the asymmetric aldol reaction-Reference-Cited by-同舟云学术

Highly efficient organocatalysts for the asymmetric aldol reaction

Published:2018 Issue:9 Volume:42 Page:7416-7421
ISSN:1144-0546
Container-title:New Journal of Chemistry
language:en
Short-container-title:New J. Chem.

Author:

Jacoby C. G.¹²³⁴^ORCID,Vontobel P. H. V.¹²³⁴,Bach M. F.¹²³⁴,Schneider P. H.¹²³⁴^ORCID

Affiliation:

1. Instituto de Química

2. Universidade Federal do Rio Grande do Sul (UFRGS)

3. 91501-970 Porto Alegre

4. Brazil

Abstract

A new class of bifunctional organocatalysts containing both thiazolidine/pyrrolidine and imidazole cycles was prepared via a readily available synthetic route.

Funder

Coordenação de Aperfeiçoamento de Pessoal de Nível Superior

Fundação de Amparo à Pesquisa do Estado do Rio Grande do Sul

Conselho Nacional de Desenvolvimento Científico e Tecnológico

Publisher

Royal Society of Chemistry (RSC)

Subject

Materials Chemistry,General Chemistry,Catalysis

Link

http://pubs.rsc.org/en/content/articlepdf/2018/NJ/C7NJ04424K

Reference46 articles.

1. The advent and development of organocatalysis

2. Asymmetric Aminocatalysis-Gold Rush in Organic Chemistry

3. Proline-Catalyzed Direct Asymmetric Aldol Reactions

4. Total synthesis of natural and pharmaceutical products powered by organocatalytic reactions

Cited by 16 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. Dipeptide-catalysed Michael reaction under physiological conditions: Examination of potential bioorthogonality;Bioorganic & Medicinal Chemistry;2024-04

2. Organocatalytic Synthesis and DNA Interactive Studies of New 1,2,3‐triazolyl‐thiazolidines Hybrids;ChemBioChem;2024-02-28

3. Pyrrolidine-oxadiazolone conjugate as new organocatalyst for asymmetric aldol condensation;Synthetic Communications;2023-04-25

4. Poly(ε-caprolactones) Initiated by Chiral Compounds: A New Protocol to Support Organocatalysts;Catalysts;2023-01-10

5. Organo-catalysis as emerging tools in organic synthesis: aldol and Michael reactions;Physical Sciences Reviews;2022-01-05