What type of study is this?

September 10, 2025ACS Catalysis

Palladium-Catalyzed Aerobic Alkene Arylboration: Coupling Aryl Boronic Acids, Alkenes, and Bis(pinacol)diboron

View Full Paper

Ask AI

Bookmark

Authors

HPHoang T. P. PhamThe University of Texas at Austin SBShreeja BhattThe University of Texas at Austin KHKami L. HullThe University of Texas at Austin

Discussion

Member takes

Implication

This method demonstrates efficient alkyl boronic ester formation from aryl boronic acids and alkenes, indicating potential for streamlined synthetic processes.

Key Points

The method allows direct access to alkyl boronic esters in one step, simplifying synthesis.
Isolated yields of alkyl boronic esters ranged from 20 to 74%, showcasing synthetic utility.
Three-component reactions utilize aryl boronic acids, alkenes, and bis(pinacol)diboron effectively.
The involvement of π-benzyl intermediates highlights the complexity of the catalytic cycle.

Cite This Study

Pham et al. (2025) studied this question.

synapsesocial.com/papers/68c1bb7054b1d3bfb60ed8cf https://doi.org/10.1021/acscatal.5c03926

View Full Paper

Ask AI

Bookmark

Implication

This method demonstrates efficient alkyl boronic ester formation from aryl boronic acids and alkenes, indicating potential for streamlined synthetic processes.

Palladium-Catalyzed Aerobic Alkene Arylboration: Coupling Aryl Boronic Acids, Alkenes, and Bis(pinacol)diboron

Discussion

Member takes

Implication

Key Points

Cite This Study

Palladium-Catalyzed Aerobic Alkene Arylboration: Coupling Aryl Boronic Acids, Alkenes, and Bis(pinacol)diboron

Discussion

Member takes

Implication

Key Points

Cite This Study

Also Consider

Also Consider