4962-31-6Relevant articles and documents
Reactions of alkenes, alkynes, and alkoxyallenes with new polymer-supported electrophilic reagents
Monenschein, Holger,Sourkouni-Argirusi, Georgia,Schubothe, Katherine M.,O'Hare, Thomas,Kirschning, Andreas
, p. 2101 - 2104 (2008/02/09)
(matrix presented) Preparation of new polymer-supported electrophilic reagents that efficiently promote 1,2-haloacetoxylations of alkenes and alkoxyallenes is described. Under very mild conditions and in high yields, alkenes are transformed into α-halo acetates while alkoxyallenes lead to vinyl iodides. In contrast to these results, terminal alkynes commonly afford synthetically valuable 1-iodo-alkynes. ? Technischen Universitaet Clausthal. ? Willamette University.
STEREOCHEMISTRY AND REGIOCHEMISTRY OF THE ADDITION OF HYPOBROMOUS ACID TO β-METHYLSTYRENES
Marples, B. A.,Saint, C. G.
, p. 545 - 556 (2007/10/02)
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