Enolate-Based Regioselective Anti-Beckmann C–C Bond Cleavage of Ketones-Reference-Cited by-同舟云学术

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Enolate-Based Regioselective Anti-Beckmann C–C Bond Cleavage of Ketones

Published:2021-08-09 Issue:17 Volume:86 Page:11608-11632
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Mašek Tomáš¹,Jahn Ullrich¹^ORCID

Affiliation:

1. Institute of Organic Chemistry and Biochemistry of the Czech Academy of Sciences, Flemingovo náměstí 542/2, 166 10 Prague 6, Czech Republic

Funder

GrantovÃ¡ Agentura Ä?eskÃ© Republiky

Univerzita Karlova v Praze

Gilead Sciences & IOCB Research Center

Institute of Organic Chemistry and Biochemistry of the Czech Academy of Sciences

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.joc.1c01169

Reference81 articles.

1. a Special issue on C-C bond cleavage in stereoselective synthesis: Chem. Rev. 2021, 121, issue 1.

2. Selective Carbon–Carbon Bond Cleavage of Cyclopropanols

3. Transition Metal-Catalyzed Selective Carbon–Carbon Bond Cleavage of Vinylcyclopropanes in Cycloaddition Reactions

4. Creating Stereocenters within Acyclic Systems by C–C Bond Cleavage of Cyclopropanes

5. Catalytic Enantioselective Ring-Opening Reactions of Cyclopropanes

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3. Water-mediated decarboxylative radical nitrosation of β-keto acids with tert-butyl nitrite: access to α-oximino ketones;New Journal of Chemistry;2022

4. Kinetic vs. thermodynamic control of β-functionalized cyclic ketones: a theoretical investigation of regioselective formation of enolates;Organic Chemistry Frontiers;2022

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