ISUDR
metadata only
Free radical reactions of allylic and propargylic derivatives
Addition of tert-butyl radical, generated from t-BuHgCl, to allyl or propargyl derivatives forms adduct radicals which can undergo [beta]-elimination with substituents such as halogen, PhS, PhSO[subscript]2 to form the alkyl-substituted propene or allene and an eliminated radical which regenerate
Conceptio Open Archive
Analyze & explore related research in Conceptio
Connect this record directly into your research workflow or AI agent. Explore citations across open repositories, query full text, and export structured proof bundles.
This document is indexed with metadata only: full text is not available in the archive for this record. Open the official source ↗
Related documents
- Natural Product Synthesis Enabled by Radical-Polar Crossover Reactions#667108
- Catalytic C−C bond cleavage of propargylic alcohols to alkynes and ketones#978752
- An Introduction to Free-Radical Chemistry#1179995
- Photolysis of allene and propyne in the 7–30eV region probed by the visible fluorescence of their fragments#391891
- Urea-enabled diene functionalization reactions via palladium π-allyl complexes#1148753
Record · ID 964196
Retrieved via Conceptio: every document is proof-bundled with source, license, and retrieval metadata.
Retrieved via Conceptio: every document is proof-bundled with source, license, and retrieval metadata.
Bring this data into your agent: Connect via MCP or API · 20 free credits to start · no card required
Read the Docs → · View CLI source on GitHub · Conceptio Open Knowledge Archive
Read the Docs → · View CLI source on GitHub · Conceptio Open Knowledge Archive