Efficient synthesis of isotopically pure [O-18]-epoxides using molecular oxygen

Schöttler, M.; Boland, W.

Item

ITEM ACTIONSEXPORT

Add to Basket

Local TagsRelease HistoryDetailsSummary

Released

Journal Article

Efficient synthesis of isotopically pure [O-18]-epoxides using molecular oxygen

MPS-Authors

/persons/resource/persons3812

Boland, W.
Department of Bioorganic Chemistry, MPI for Chemical Ecology, Max Planck Society;

External Resource

No external resources are shared

Fulltext (restricted access)

There are currently no full texts shared for your IP range.

Fulltext (public)

There are no public fulltexts stored in PuRe

Supplementary Material (public)

There is no public supplementary material available

Citation

Schöttler, M., & Boland, W. (1997). Efficient synthesis of isotopically pure [O-18]-epoxides using molecular oxygen. Synlett, (1), 91.

Cite as: https://hdl.handle.net/11858/00-001M-0000-0012-A343-6

Abstract

High yields of isotopically pure [O-18]-epoxides are obtained from alkenes and O-18(2) gas in the presence of isobutyraldehyde (Kaneda epoxidation). Unlike peracids, the system allows the selective epoxidation of the double bond in a keto-alkene without