180069-66-3Relevant articles and documents
N -heterocyclic carbene organocatalytic reductive β,β-coupling reactions of nitroalkenes via radical intermediates
Du, Yu,Wang, Yuhuang,Li, Xin,Shao, Yaling,Li, Guohui,Webster, Richard D.,Chi, Yonggui Robin
, p. 5678 - 5681 (2014)
An unprecedented N-heterocyclic carbene catalytic reductive β,β-carbon coupling of α,β-nitroalkenes, by using an organic substrate to mimic the one-electron oxidation role of the pyruvate ferredoxin oxidoreductase (PFOR) in living systems, has been develo
Additions of organomanganese reagents to conjugated nitroolefins
Namboothiri,Hassner, Alfred
, p. 69 - 77 (2007/10/03)
Additions of organomanganese reagents to aromatic and aliphatic conjugated nitroolefins were examined for the first time. In most cases reaction proceeded rapidly at -30°C. Unlike Mn reagents lacking β-hydrogens (Me, Ph), which lead to oxidative coupling and reductive dimerisation of nitrostyrenes, benzylmanganese chloride gives 1,4-addition in yields exceeding Grignard or Cu-assisted additions. At 0°C alkyl(Bu, Pr)-manganese reagents undergo an addition-migration-elimination process with nitrostyrenes providing a convenient and stereospecific entry into arylated trans-olefins.