Experimental and Computational Studies on Cobalt(I)‐Catalyzed Regioselective Allylic Alkylation Reactions

Author:

Andreetta Philip1,Martin Robert T.2,Souilah Charafa1,Rentería‐Gómez Ángel3,Song Zhihui2,Khorramshahi Bayat Yas1,Ivlev Sergei1,Gutierrez Osvaldo3ORCID,Casitas Alicia1ORCID

Affiliation:

1. Fachbereich Chemie Philipps-Universität Marburg Hans-Meerwein-Straße 4 35043 Marburg Germany

2. Department of Chemistry and Biochemistry University of Maryland College Park. 8051 Regents Dr, College Park Maryland 20742 USA

3. Department of Chemistry Texas A&M University, College Station Texas 77843 USA

Abstract

AbstractHere, we report the development of cobalt(I)‐catalyzed regioselective allylic alkylation reactions of tertiary allyl carbonates with 1,3‐dicarbonyl compounds. A family of well‐defined tetrahedral cobalt(I) complexes bearing commercially available bidentate bis(phosphine) ligands [(P,P)Co(PPh3)Cl] are synthesized and explored as catalysts in allylic alkylation reactions. The catalyst [(dppp)Co(PPh3)Cl] (dppp=1,3‐Bis(diphenylphosphino)propane) enables the alkylation of a large variety of tertiary allyl carbonates with high yields and excellent regioselectivity for the branched product. Remarkably, this methodology is selective for the activation of tertiary allyl carbonates even in the presence of secondary allyl carbonates. This contrasts with the selectivity observed in cobalt‐catalyzed allylic alkylations enabled by visible light photocatalysis. Mechanistic insights by means of experimental and computational investigations support a Co(I)/Co(III) catalytic cycle.

Funder

Philipps-Universität Marburg

Camille and Henry Dreyfus Foundation

Welch Foundation

Foundation for the National Institutes of Health

Publisher

Wiley

Subject

General Medicine

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