Probing α‐Amino Aldehydes as Weakly Acidic Pronucleophiles: Direct Access to Quaternary α‐Amino Aldehydes by an Enantioselective Michael Addition Catalyzed by Brønsted Bases-Reference-Cited by-同舟云学术

Probing α‐Amino Aldehydes as Weakly Acidic Pronucleophiles: Direct Access to Quaternary α‐Amino Aldehydes by an Enantioselective Michael Addition Catalyzed by Brønsted Bases

Published:2020-12-23 Issue:7 Volume:27 Page:2483-2492
ISSN:0947-6539
Container-title:Chemistry – A European Journal
language:en
Short-container-title:Chem. Eur. J.

Author:

García‐Urricelqui Ane¹^ORCID,Cózar Abel¹²^ORCID,Mielgo Antonia¹^ORCID,Palomo Claudio¹^ORCID

Affiliation:

1. Departamento de Química Orgánica I Universidad del País Vasco UPV/EHU Manuel Lardizábal 3 20018 San Sebastián Spain

2. IKERBASQUE Basque Foundation for Science 48009 Bilbao Spain

Funder

Eusko Jaurlaritza

Ministerio de Ciencia, Innovación y Universidades

Euskal Herriko Unibertsitatea

Publisher

Wiley

Subject

General Chemistry,Catalysis,Organic Chemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/chem.202004468

Reference163 articles.

1. For reviews on α-amino aldehydes see:

2. Synthesis of Chiral Amines Using α‐Amino Aldehydes

3. Synthesis and reactivity ofN-protected-?-amino aldehydes

4. The Synthesis of Vicinal Amino Alcohols

5. Synthesis and Diastereoselective Reactions of N,N-Dibenzylamino Aldehydes and Related Compounds

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