Vanadium-Mediated Carbon Isotope Exchange of Terminal Alkenes

The incorporation of carbon isotopes into bioactive compounds is of great importance in chemistry, biology, and medicine. Especially valuable are catalytic procedures that rely on a limited collection of available labeled materials. Recently we introduced a conceptually novel solution to carbon isotope exchange (CIE) for terminal olefins based on the preference of V alkylidenes for degenerate metathesis. However, the previous report utilized a V catalyst that suffered from functional group tolerance due to the high electrophilicity of the V center, making it impractical for biological compounds. Herein, we utilized V catalysts containing electron-donating groups to overcome those challenges. We utilize isotopically labeled substituted styrene as a labeled ═<sup>13</sup>CH<sub>2</sub> moiety source, prepared from <sup>13</sup>C-labeled iodomethane. The isotope source can be easily removed from the reaction mixture, recovered, and reused. A diverse range of terminal alkenes, including bioactive molecules, were tested to showcase the capabilities and limitations of the developed method.

Authors

Institutions

Publication Details

Journal
Journal of the American Chemical Society
Published
2025-06-06
DOI
https://doi.org/10.1021/jacs.5c05880
Citations
7
Primary Topic
Chemical Reactions and Isotopes
Type
article
Field-Weighted Citation Impact
5.54

Funders

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Vanadium-Mediated Carbon Isotope Exchange of Terminal Alkenes

Vasilisa Krivovicheva, Konstantin V. Bukhryakov, Leonardo B. Maya, Alexander Moiseevich Mebel et al.
7 citations
Journal of the American Chemical Society
Chemical Reactions and Isotopes
5.54
article

Vanadium-Mediated Carbon Isotope Exchange of Terminal Alkenes

Vasilisa Krivovicheva, Konstantin V. Bukhryakov, Leonardo B. Maya, Alexander Moiseevich Mebel, Anqi Liu, Madhu Sudhana Reddy Gangireddy
article en
7 citations

Abstract

The incorporation of carbon isotopes into bioactive compounds is of great importance in chemistry, biology, and medicine. Especially valuable are catalytic procedures that rely on a limited collection of available labeled materials. Recently we introduced a conceptually novel solution to carbon isotope exchange (CIE) for terminal olefins based on the preference of V alkylidenes for degenerate metathesis. However, the previous report utilized a V catalyst that suffered from functional group tolerance due to the high electrophilicity of the V center, making it impractical for biological compounds. Herein, we utilized V catalysts containing electron-donating groups to overcome those challenges. We utilize isotopically labeled substituted styrene as a labeled ═<sup>13</sup>CH<sub>2</sub> moiety source, prepared from <sup>13</sup>C-labeled iodomethane. The isotope source can be easily removed from the reaction mixture, recovered, and reused. A diverse range of terminal alkenes, including bioactive molecules, were tested to showcase the capabilities and limitations of the developed method.

Journal of the American Chemical SocietyVol. 147(24)
Florida International University (US)
National Institute of General Medical Sciences
Openalex Percentile: Top 4%
Chemical Reactions and Isotopes
5.54
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.

Vanadium-Mediated Carbon Isotope Exchange of Terminal Alkenes — Vasilisa Krivovicheva, Konstantin V. Bukhryakov, et al. · Journal of the American Chemical Society (2025) | TGRS Research Map | TGRS