Organocatalytic Synthesis of γ-Amino Acid Precursors via Masked Acetaldehyde under Micellar Catalysis

The development of micellar catalysis offers a sustainable alternative to organic solvents, and represents an environmental milestone in organic synthesis. Here, the first Michael addition of masked acetaldehyde under neutral, cationic and anionic micellar catalysis is reported, affording the produc...

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Main Authors: Maria Edith Casacchia, Giuliana Giorgianni, Elena Allegritti, Luisa Giansanti, Armando Carlone, Fabio Pesciaioli
Format: Article
Language:English
Published: Georg Thieme Verlag KG 2023-01-01
Series:SynOpen
Subjects:
Online Access:http://www.thieme-connect.de/DOI/DOI?10.1055/a-1996-8940
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author Maria Edith Casacchia
Giuliana Giorgianni
Elena Allegritti
Luisa Giansanti
Armando Carlone
Fabio Pesciaioli
author_facet Maria Edith Casacchia
Giuliana Giorgianni
Elena Allegritti
Luisa Giansanti
Armando Carlone
Fabio Pesciaioli
author_sort Maria Edith Casacchia
collection DOAJ
description The development of micellar catalysis offers a sustainable alternative to organic solvents, and represents an environmental milestone in organic synthesis. Here, the first Michael addition of masked acetaldehyde under neutral, cationic and anionic micellar catalysis is reported, affording the products in high yields and enantiomeric excess, despite the use of water as solvent.
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spelling doaj.art-0429bd57400546d5933b3b7da4acd3ee2023-01-31T00:21:24ZengGeorg Thieme Verlag KGSynOpen2509-93962023-01-010701293210.1055/a-1996-8940Organocatalytic Synthesis of γ-Amino Acid Precursors via Masked Acetaldehyde under Micellar CatalysisMaria Edith Casacchia0Giuliana Giorgianni1Elena Allegritti2Luisa Giansanti3Armando Carlone4Fabio Pesciaioli5Dipartimento di Scienze Fisiche e Chimiche, Università degli Studi dell’AquilaDipartimento di Scienze Fisiche e Chimiche, Università degli Studi dell’AquilaDipartimento di Scienze Fisiche e Chimiche, Università degli Studi dell’AquilaDipartimento di Scienze Fisiche e Chimiche, Università degli Studi dell’AquilaDipartimento di Scienze Fisiche e Chimiche, Università degli Studi dell’AquilaDipartimento di Scienze Fisiche e Chimiche, Università degli Studi dell’AquilaThe development of micellar catalysis offers a sustainable alternative to organic solvents, and represents an environmental milestone in organic synthesis. Here, the first Michael addition of masked acetaldehyde under neutral, cationic and anionic micellar catalysis is reported, affording the products in high yields and enantiomeric excess, despite the use of water as solvent.http://www.thieme-connect.de/DOI/DOI?10.1055/a-1996-8940micellar catalysisaminocatalysisasymmetric synthesisγ-amino acidsgreen chemistry
spellingShingle Maria Edith Casacchia
Giuliana Giorgianni
Elena Allegritti
Luisa Giansanti
Armando Carlone
Fabio Pesciaioli
Organocatalytic Synthesis of γ-Amino Acid Precursors via Masked Acetaldehyde under Micellar Catalysis
SynOpen
micellar catalysis
aminocatalysis
asymmetric synthesis
γ-amino acids
green chemistry
title Organocatalytic Synthesis of γ-Amino Acid Precursors via Masked Acetaldehyde under Micellar Catalysis
title_full Organocatalytic Synthesis of γ-Amino Acid Precursors via Masked Acetaldehyde under Micellar Catalysis
title_fullStr Organocatalytic Synthesis of γ-Amino Acid Precursors via Masked Acetaldehyde under Micellar Catalysis
title_full_unstemmed Organocatalytic Synthesis of γ-Amino Acid Precursors via Masked Acetaldehyde under Micellar Catalysis
title_short Organocatalytic Synthesis of γ-Amino Acid Precursors via Masked Acetaldehyde under Micellar Catalysis
title_sort organocatalytic synthesis of γ amino acid precursors via masked acetaldehyde under micellar catalysis
topic micellar catalysis
aminocatalysis
asymmetric synthesis
γ-amino acids
green chemistry
url http://www.thieme-connect.de/DOI/DOI?10.1055/a-1996-8940
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