Light Up the Transition Metal-Catalyzed Single-Electron Allylation-Reference-Cited by-同舟云学术

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Light Up the Transition Metal-Catalyzed Single-Electron Allylation

Published:2020-08 Issue:8 Volume:2 Page:764-775
ISSN:2589-5974
Container-title:Trends in Chemistry
language:en
Short-container-title:Trends in Chemistry

Author:

Zhang Mao-Mao,Wang Ya-Ni,Lu Liang-Qiu,Xiao Wen-Jing

Funder

National Science Foundation of China

Program of Introducing Talents of Discipline to Universities of China

Natural Science Foundation of Hubei Province

Publisher

Elsevier BV

Subject

General Chemistry

Reference99 articles.

1. Organic syntheses by means of noble metal compounds XVII. Reaction of π-allylpalladium chloride with nucleophiles;Tsuji;Tetrahedron Lett.,1965

2. Carbon—carbon bond formation via palladium complexes;Tsuji;Acc. Chem. Res.,1969

3. Asymmetric induction in catalytic allylic alkylation;Trost;J. Am. Chem. Soc.,1977

4. Asymmetric transition metal-catalyzed allylic alkylations;Trost;Chem. Rev.,1996

5. Asymmetric transition-metal-catalyzed allylic alkylations: applications in total synthesis;Trost;Chem. Rev.,2003

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1. Asymmetric radical allylation of β-keto esters with vinyl cyclopropanes by dual photoredox/nickel catalysis;Science China Chemistry;2024-08-27

2. Photochemical Asymmetric Palladium-Catalyzed Allylation Reaction: Expeditious Entry to Chiral 1,2-Amino Alcohols and 1,2-Diamines;ACS Catalysis;2024-08-23

3. Rh-Catalyzed Asymmetric Allylic Substitution with Photo-Generated Alkyl Radical Species;ACS Catalysis;2024-08-05

4. Cobalt‐Catalyzed Allylic Alkylation at sp³‐Carbon Centers;Chemistry – A European Journal;2024-08-02

5. Cross-Double Deoxygenative Carbon–Carbon Bond Formation between Benzyl Benzoates and Allylic Alcohols;ACS Catalysis;2024-06-10

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