Epoxide, a cyclic ether, can be used to obtain important alcohols, pharmaceuticals, agrochemicals, and functional polymers. This transformation is facilitated by the reductive ring opening of epoxide.

This review is led by Prof. Yuchao Zhang (Key Laboratory of Photochemistry, CAS Research/Education Center for Excellence in Molecular Sciences, Institute of Chemistry, Chinese Academy of Sciences).

Rather than form the thiirane directly from an olefin or similar, List and co-workers suggest instead starting with the far more accessible epoxides. Noting that thiolactams undergo an exchange ...

This module covers synthesis and reactivity of ethers and epoxides. Students will connect these to the larger sustainability goals of UNSDG 3: Good Health and Well-being, 9: Industry, Innovation, and ...

Two studies report the first isolation of α-boryl aldehydes, bifunctional reagents that facilitate synthesis of organic compounds that were previously difficult or impossible to make. The work could ...

Can making ephemeral anti-inflammatory fatty acids stick around a little longer protect people against Alzheimer’s disease? It just might, according to a study by Hui Zheng and colleagues at the ...

Epoxides belong to a class of organic compounds called “cyclic ethers” that are characterized by a three-atom ring. They are readily available compounds found in medicinal and agrochemical agents, as ...