Stereospecific Decarboxylative Benzylation of Enolates: Development and Mechanistic Insight-Reference-Cited by-同舟云学术

Stereospecific Decarboxylative Benzylation of Enolates: Development and Mechanistic Insight

Published:2018-03-13 Issue:7 Volume:20 Page:1730-1734
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Li Tian-Ren¹²³,Maliszewski Mary L.¹²,Xiao Wen-Jing³^ORCID,Tunge Jon A.¹²^ORCID

Affiliation:

1. Department of Chemistry, The University of Kansas, 2010 Malott Hall, 1251 Wescoe Hall Drive, Lawrence, Kansas 66045, United States

2. The KU Chemical Methodologies and Library Development Center of Excellence, 2034 Becker Drive, Lawrence, Kansas 66047, United States

3. Key Laboratory of Pesticide & Chemical Biology Ministry of Education, College of Chemistry, Central China Normal University, 152 Luoyu Road, Wuhan, Hubei 430079, China

Funder

Division of Chemistry

Kansas Bioscience Authority

China Scholarship Council

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.8b00169

Reference74 articles.

1. Transition Metal-Catalyzed Decarboxylative Allylation and Benzylation Reactions

2. Transition metal-catalyzed decarboxylative cross-coupling reactions

3. Decarboxylative coupling reactions: a modern strategy for C–C-bond formation

4. Carboxylates as sources of carbon nucleophiles and electrophiles: comparison of decarboxylative and decarbonylative pathways

5. Facile generation of a reactive palladium(II) enolate intermediate by the decarboxylation of palladium(II) .beta.-ketocarboxylate and its utilization in allylic acylation

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