What type of study is this?

This is a Experimental Study study.

A Catalyst‐Free, Transition‐Metal‐Free, and Selective Chloro‐Alkoxylation of Olefins with Alcohols and tert‐Butyl Hypochlorite

View Full Paper

Ask AI

Bookmark

Authors

This method demonstrates effective chloroalkoxylation of olefins using tert-butyl hypochlorite, indicating new prospects for organic synthesis.

A catalyst-free method achieves chloroalkoxylation with good regioselectivity in transforming olefins.
Using tert-butyl hypochlorite, the process yields a variety of β-chloroethyl ethers from alkenes.
The reaction also allows diastereoselective outcomes for α,β-unsaturated compounds, enhancing product diversity.
This approach supports the late-stage functionalization of complex substrates, indicating wide application potential.

Sun et al. (2025) studied this question.

View Full Paper

Ask AI

Bookmark

This method demonstrates effective chloroalkoxylation of olefins using tert-butyl hypochlorite, indicating new prospects for organic synthesis.