α‐Branched Ketone Dienolates: Base‐Catalysed Generation and Regio‐ and Enantioselective Addition Reactions-Reference-Cited by-同舟云学术

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α‐Branched Ketone Dienolates: Base‐Catalysed Generation and Regio‐ and Enantioselective Addition Reactions

Published:2019-07-03 Issue:41 Volume:25 Page:9701-9709
ISSN:0947-6539
Container-title:Chemistry – A European Journal
language:en
Short-container-title:Chem. Eur. J.

Author:

Urruzuno Iñaki¹,Mugica Odei¹,Zanella Giovanna¹,Vera Silvia¹,Gómez‐Bengoa Enrique¹,Oiarbide Mikel¹,Palomo Claudio¹^ORCID

Affiliation:

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

Funder

Euskal Herriko Unibertsitatea

Eusko Jaurlaritza

Secretaría de Estado de Investigación, Desarrollo e Innovación

Horizon 2020 Framework Programme

Publisher

Wiley

Subject

General Chemistry,Catalysis,Organic Chemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/chem.201901694

Reference170 articles.

1. Direct Asymmetric Alkylation of Ketones: Still Unconquered

2. Direkte asymmetrische Alkylierung von Ketonen: noch immer ein unerreichtes Ziel

3.

4. The Vinylogous Aldol and Related Addition Reactions: Ten Years of Progress

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2. Brønsted Base‐Catalyzed Enantioselective α‐Functionalization of Carbonyl Compounds Involving π‐Extended Enolates;The Chemical Record;2023-06-23

3. Sterically Hindered and Deconjugative α‐Regioselective Asymmetric Mannich Reaction of Meinwald Rearrangement‐Intermediate;Angewandte Chemie International Edition;2023-02-13

4. Sterically Hindered and Deconjugative α‐Regioselective Asymmetric Mannich Reaction of Meinwald Rearrangement‐Intermediate;Angewandte Chemie;2023-02-13

5. Progress in catalytic asymmetric α-functionalization of vinylogous nucleophilic species;Organic Chemistry Frontiers;2023

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