tert-Butyl ester or benzylamide of the dipeptide Pro-Gly as organocatalysts for the asymmetric aldol reaction-Reference-Cited by-同舟云学术

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tert-Butyl ester or benzylamide of the dipeptide Pro-Gly as organocatalysts for the asymmetric aldol reaction

Published:2015-02 Issue:6 Volume:71 Page:932-940
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Triandafillidi Ierasia,Bisticha Aikaterini,Voutyritsa Errika,Galiatsatou Gerasimia,Kokotos Christoforos G.

Funder

Education and Lifelong Learning

ESF

ORCA COST Action

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference90 articles.

1. For books, see:

2. Asymmetric Organocatalysis – from Biomimetic Concepts to Powerful Methods for Asymmetric Synthesis;Berkessel,2005

3. Enantioselective Organocatalysis Reactions and Experimental Procedure;Dalko,2007

4. For selected reviews, see:

5. Enamine Catalysis

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1. Prolinamides derived from 2-aminocyclohexanols as organocatalysts for asymmetric List-Lerner-Barbas aldol reactions;Tetrahedron Letters;2024-04

2. Prolinamides containing 2-(2-aminocyclohexyl)phenols as highly enantioselective organocatalysts for aldol reactions;Organic & Biomolecular Chemistry;2023

3. Both Amide-Bearing α- and β-Amino Acids from Natural Aspartic Acid Are Efficient Organocatalysts for Enantioselective Aldol Reactions;Synthesis;2022-09-29

4. ASYMMETRIC PEPTIDE CATALYSIS;Catalytic Asymmetric Synthesis;2022-06-03

5. Pro‐Pro Dipeptide‐Thiourea Organocatalyst in the Mannich Reaction between α‐Imino Esters and Pyruvates;European Journal of Organic Chemistry;2022-05-12

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