82959-71-5Relevant academic research and scientific papers
On the mechanism of the tetrathiafulvalene-mediated radical-polar crossover reactions
Bashir, Nadeem,Callaghan, Owen,Murphy, John A.,Ravishanker,Roome, Stephen J.
, p. 6255 - 6258 (1997)
Strong evidence supports the previously proposed mechanism of the radical-polar crossover reactions, and discounts a totally ionic mechanism.
CARBOCYCLIZATION BY HOMOLYTIC SUBSTITUTION (SH' PROCESS). A NEW ROUTE TO DIHYDROINDOLE OR DIHYDROBENZOFURAN
Ueno, Yoshio,Chino, Kunitake,Okawara, Makoto
, p. 2575 - 2576 (2007/10/02)
N-(4-Phenyltio-2-butenyl)-2-bromoaniline reacted with tributyltin hydride to give 3-vinyl-2,3-dihydroindole in 96percent yield via hitherto unknown intramolecular SH' process, some other examples and remarkable dilution effect on these homolytic carbocyclizations were described.
