1224637-00-6Relevant articles and documents
Selective reduction of amides to amines by boronic acid catalyzed hydrosilylation
Li, Yuehui,Molina De La Torre, Jesus A.,Grabow, Kathleen,Bentrup, Ursula,Junge, Kathrin,Zhou, Shaolin,Brueckner, Angelika,Beller, Matthias
, p. 11577 - 11580 (2013)
Not a 'B'ore! Benzothiophene-based boronic acids catalyze the reduction of tertiary, secondary, and primary amides in the presence of a hydrosilane. The reaction demonstrates good functional-group tolerance. Copyright
Synthesis of Lepadiformine Using a Hydroamination Transform
Tabor, M. Greg,Shenvi, Ryan A.
, p. 5776 - 5779 (2015/12/11)
Dissection of lepadiformine by a double hydroamination transform affords a simple achiral amino diene. This reaction is accomplished in the forward sense by amine-directed hydroboration and an oxidative alkyl shift to nitrogen, both of which occur with hi
