Enantioselective rhodium-catalysed insertion of trifluorodiazoethanes into tin hydrides
Aryl substituted 2,2,2-trifluorodiazoethanes undergo rhodium(II)-catalysed insertion reactions with tin hydrides affording the corresponding α-(trifluoromethyl)benzyl stannanes. This reactivity contrasts with that of diazo esters which predominantly afford CH2 reduction products in the presence of t...
Үндсэн зохиолчид: | Hyde, S, Veliks, J, Ascough, D, Szpera, R, Paton, R, Gouverneur, V |
---|---|
Формат: | Journal article |
Хэл сонгох: | English |
Хэвлэсэн: |
Elsevier
2018
|
Ижил төстэй зүйлс
-
Rhodium-catalysed regio- and enantioselective Suzuki-Miyaura cross-coupling reactions
-н: Liu, K
Хэвлэсэн: (2023) -
Rhodium-catalysed intermolecular alkyne hydroacylation: the enantioselective synthesis of α- and β-substituted ketones by kinetic resolution.
-н: González-Rodríguez, C, зэрэг
Хэвлэсэн: (2010) -
New reactivity and selectivity in rhodium-catalysed hydroacylation
-н: Pal, R
Хэвлэсэн: (2020) -
New applications of rhodium-catalysed hydroacylation
-н: Iwumene, NUN
Хэвлэсэн: (2022) -
Mechanistic studies of rhodium-catalysed intermolecular hydroacylation
-н: Barwick-Silk, J
Хэвлэсэн: (2018)