Enantioselective organocatalytic syntheses of α-selenated α- and β-amino acid derivatives-Reference-Cited by-同舟云学术

Enantioselective organocatalytic syntheses of α-selenated α- and β-amino acid derivatives

Published:2022 Issue:4 Volume:20 Page:824-830
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Haider Victoria¹,Zebrowski Paul¹^ORCID,Michalke Jessica²,Monkowius Uwe³^ORCID,Waser Mario¹^ORCID

Affiliation:

1. Institute of Organic Chemistry, Johannes Kepler University Linz, Altenbergerstrasse 69, 4040 Linz, Austria

2. Institute of Catalysis, Johannes Kepler University Linz, Altenbergerstrasse 69, 4040 Linz, Austria

3. School of Education, Chemistry, Johannes Kepler University Linz, Altenbergerstrasse 69, 4040 Linz, Austria

Abstract

The enantioselective electrophilic α-selenation of masked α- and β-amino acid derivatives has been carried under organocatalytic conditions in good yields and with moderate to good enantioselectivities.

Funder

Austrian Science Fund

European Commission

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2022/OB/D1OB02235K

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4. Recent approaches towards the asymmetric synthesis of α,α-disubstituted α-amino acids

5. Recent progress on the stereoselective synthesis of cyclic quaternary α-amino acids

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