A highly enantio- and diastereoselective direct aldol reaction in aqueous medium catalyzed by thiazolidine-based compounds-Reference-Cited by-同舟云学术

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A highly enantio- and diastereoselective direct aldol reaction in aqueous medium catalyzed by thiazolidine-based compounds

Published:2015-07 Issue:12-13 Volume:26 Page:632-637
ISSN:0957-4166
Container-title:Tetrahedron: Asymmetry
language:en
Short-container-title:Tetrahedron: Asymmetry

Author:

Rambo Raoní Scheibler,Gross Jacoby Caroline,da Silva Tiago Lima,Schneider Paulo Henrique

Funder

CAPES

CNPq

INCT-CMN

FAPERGS

Publisher

Elsevier BV

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Catalysis

Reference38 articles.

1. Recent Advances in Organocatalytic Methods for Asymmetric CC Bond Formation

2. Asymmetric organocatalytic cycloadditions

3. Organocatalysis—after the gold rush

4. The advent and development of organocatalysis

5. Asymmetric Aminocatalysis-Gold Rush in Organic Chemistry

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

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

3. Recent developments in next generation (S)-proline-derived chiral organocatalysts;Tetrahedron;2021-05

4. Chiral Thiazolidine based Organocatalysts: Synthesis and Application in Asymmetric Aldol Reactions;Letters in Organic Chemistry;2020-04-28

5. Asymmetric Michael reaction promoted by chiral thiazolidine-thiourea catalyst;Tetrahedron;2020-01

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