Palladium-Catalyzed Enantioselective β-C(sp<sup>3</sup>)–H Activation Reactions of Aliphatic Acids: A Retrosynthetic Surrogate for Enolate Alkylation and Conjugate Addition-Reference-Cited by-同舟云学术

Palladium-Catalyzed Enantioselective β-C(sp³)–H Activation Reactions of Aliphatic Acids: A Retrosynthetic Surrogate for Enolate Alkylation and Conjugate Addition

Published:2022-01-25 Issue:4 Volume:55 Page:537-550
ISSN:0001-4842
Container-title:Accounts of Chemical Research
language:en
Short-container-title:Acc. Chem. Res.

Author:

Lucas Erika L.¹,Lam Nelson Y. S.¹^ORCID,Zhuang Zhe¹^ORCID,Chan Hau Sun Sam¹^ORCID,Strassfeld Daniel A.¹,Yu Jin-Quan¹^ORCID

Affiliation:

1. Department of Chemistry, The Scripps Research Institute, 10550 N. Torrey Pines Road, La Jolla, California 92037, United States

Funder

Scripps Research Institute

Royal Society of Chemistry

Croucher Foundation

Center for Selective C-H Functionalization, National Science Foundation

National Institute of General Medical Sciences

Publisher

American Chemical Society (ACS)

Subject

General Medicine,General Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.accounts.1c00672

Reference74 articles.

1. Ligand-accelerated enantioselective methylene C(sp 3 )–H bond activation

2. Formation of α-chiral centers by asymmetric β-C(sp 3 )–H arylation, alkenylation, and alkynylation

3. Ligand-Enabled β-C(sp3)–H Olefination of Free Carboxylic Acids

4. Ligand-controlled divergent dehydrogenative reactions of carboxylic acids via C–H activation

5. Ueber künstliche Bildung des Harnstoffs

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