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- W1968048629 abstract "Abstract The cyclization of several substituted hexynyl and heptynyl iodides proceeds stereoselectively to give either E- or Z-exocyclic double bonds depending on the type of precursor and radical chain used. In UniMolecular Chain Transfer (UMCT) reactions, the intramolecular abstraction of hydrogen by the intermediate vinyl radical leads exclusively to the E-isomer while the traditional tin hydride method usually provides the Z-isomer with good selectivity." @default.
- W1968048629 created "2016-06-24" @default.
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- W1968048629 date "2010-08-03" @default.
- W1968048629 modified "2023-09-26" @default.
- W1968048629 title "ChemInform Abstract: Stereoselective Hydrogen Transfer Reactions of Vinyl Radicals: Cyclization of Alkynyl Iodides by Unimolecular Chain Transfer from Silicon Hydrides." @default.
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- W1968048629 doi "https://doi.org/10.1002/chin.199735079" @default.
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