Journal
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
Volume 134, Issue 31, Pages 12924-12927Publisher
AMER CHEMICAL SOC
DOI: 10.1021/ja305694r
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Funding
- MEXT
- CREST from JST
- JSPS
- Grants-in-Aid for Scientific Research [24106701, 23850001, 24685015] Funding Source: KAKEN
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Direct C(sp(3))-H borylation of amides, ureas, and 2-aminopyridine derivatives at the position alpha to the N atom, which gives the corresponding alpha-aminoalkylboronates, has been achieved with a heterogeneous catalyst system consisting of [Rh(OMe)(cod)](2) and a silica-supported triarylphosphine ligand (Silica-TRIP) that features an immobilized triptycene-type cage structure with a bridgehead P atom. The reaction occurs not only at terminal C-H bonds but also at internal secondary C-H bonds under mild reaction conditions (25-100 degrees C, 0.1-0.5 mol % Rh).
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