Unified Approach to the Chemoselective α-Functionalization of Amides with Heteroatom Nucleophiles-Reference-Cited by-同舟云学术

Unified Approach to the Chemoselective α-Functionalization of Amides with Heteroatom Nucleophiles

Published:2019-11-12 Issue:46 Volume:141 Page:18437-18443
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Gonçalves Carlos R.¹,Lemmerer Miran¹,Teskey Christopher J.¹,Adler Pauline¹,Kaiser Daniel¹^ORCID,Maryasin Boris¹²,González Leticia²^ORCID,Maulide Nuno¹^ORCID

Affiliation:

1. Institute of Organic Chemistry, University of Vienna, Währinger Strasse 38, 1090 Vienna, Austria

2. Institute of Theoretical Chemistry, University of Vienna, Währinger Strasse 17, 1090 Vienna, Austria

Funder

Austrian Academy of Sciences

Austrian Science Fund

Universit?t Wien

Funda??o para a Ci?ncia e a Tecnologia

H2020 European Research Council

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

http://pubs.acs.org/doi/pdf/10.1021/jacs.9b06956

Reference27 articles.

1. Asymmetric alkylation reactions of chiral imide enolates. A practical approach to the enantioselective synthesis of .alpha.-substituted carboxylic acid derivatives

2. The asymmetric synthesis of .alpha.-amino acids. Electrophilic azidation of chiral imide enolates, a practical approach to the synthesis of (R)- and (S)-.alpha.-azido carboxylic acids

3. Clarification of the mechanism of rearrangement of enol silyl ether epoxides

4. Reactions of lithium enolates with molecular oxygen α-hydroxylation of amides and other carboxylate derivatives

5. Hypervalent iodine oxidation of chromium tricarbonyl complexes of benzocycloalkanones and acetophenone

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