(1,4)-Cycloaddition and C–X bond activation reactions of monovalent group 13 diyls

Group 13 diyls react with electron-rich dienes such as butadiene with (1,4)-cycloaddition, whereas oxidative addition of the C–Cl bond occurred with electron-poor hexachlorobutadienes.

Authors

T. Freese
Stephan Schulz (ORCID: https://orcid.org/0000-0003-2896-4488)
Christoph Wölper
Hanns M. Weinert (ORCID: https://orcid.org/0000-0003-1957-9430)
Pratima Dhawan

Institutions

University of Duisburg-Essen (DE)

Publication Details

Journal: Inorganic Chemistry Frontiers
Published: 2025-01-01
DOI: https://doi.org/10.1039/d5qi00660k
Primary Topic: Organic Chemistry Cycloaddition Reactions
Type: article
Field-Weighted Citation Impact: 0.00

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article

(1,4)-Cycloaddition and C–X bond activation reactions of monovalent group 13 diyls

T. Freese, Stephan Schulz, Christoph Wölper, Hanns M. Weinert et al.

Jan 1, 2025

Inorganic Chemistry Frontiers

Organic Chemistry Cycloaddition Reactions

article

(1,4)-Cycloaddition and C–X bond activation reactions of monovalent group 13 diyls

T. Freese, Stephan Schulz, Christoph Wölper, Hanns M. Weinert, Pratima Dhawan

January 1, 2025article en

Abstract

Group 13 diyls react with electron-rich dienes such as butadiene with (1,4)-cycloaddition, whereas oxidative addition of the C–Cl bond occurred with electron-poor hexachlorobutadienes.

Inorganic Chemistry FrontiersVol. 12(19)

University of Duisburg-Essen (DE)

Openalex Percentile: Top 92%

Organic Chemistry Cycloaddition Reactions

DOI Open Access PDF OpenAlex

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(1,4)-Cycloaddition and C–X bond activation reactions of monovalent group 13 diyls — T. Freese, Stephan Schulz, et al. · Inorganic Chemistry Frontiers (2025) | TGRS Research Map | TGRS