Extended Enolates: Versatile Intermediates for Asymmetric C‐H Functionalization via Noncovalent Catalysis-Reference-Cited by-同舟云学术

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Extended Enolates: Versatile Intermediates for Asymmetric C‐H Functionalization via Noncovalent Catalysis

Published:2021-06-10 Issue:40 Volume:27 Page:10226-10246
ISSN:0947-6539
Container-title:Chemistry – A European Journal
language:en
Short-container-title:Chem. Eur. J.

Author:

Oiarbide Mikel¹^ORCID,Palomo Claudio¹^ORCID

Affiliation:

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

Funder

Euskal Herriko Unibertsitatea

Eusko Jaurlaritza

Dirección General de Universidades e Investigación

Publisher

Wiley

Subject

General Chemistry,Catalysis,Organic Chemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/chem.202100756

Reference233 articles.

1. Modern Enolate Chemistry

2.

3. NEW ALDOL TYPE REACTION

4. Catalytic Asymmetric Aldol Reaction of Silyl Enol Ethers with Aldehydes by the Use of Chiral Diamine Coordinated Tin(II) Triflate

5. For selected reviews on Mukaiyama aldol reaction see:

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2. Catalytically generated noncovalent ammonium dienolate: a versatile platform for the development of organocatalytic asymmetric cascade reactions;Science China Chemistry;2024-06-26

3. Enantioselective Synthesis of the 1,3‐Dienyl‐5‐Alkyl‐6‐Oxy Motif: Method Development and Total Synthesis;Angewandte Chemie International Edition;2024-02-19

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