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...
主要な著者: | Hyde, S, Veliks, J, Ascough, D, Szpera, R, Paton, R, Gouverneur, V |
---|---|
フォーマット: | Journal article |
言語: | English |
出版事項: |
Elsevier
2018
|
類似資料
-
Rhodium-catalysed regio- and enantioselective Suzuki-Miyaura cross-coupling reactions
著者:: Liu, K
出版事項: (2023) -
Rhodium-catalysed intermolecular alkyne hydroacylation: the enantioselective synthesis of α- and β-substituted ketones by kinetic resolution.
著者:: González-Rodríguez, C, 等
出版事項: (2010) -
New reactivity and selectivity in rhodium-catalysed hydroacylation
著者:: Pal, R
出版事項: (2020) -
New applications of rhodium-catalysed hydroacylation
著者:: Iwumene, NUN
出版事項: (2022) -
Mechanistic studies of rhodium-catalysed intermolecular hydroacylation
著者:: Barwick-Silk, J
出版事項: (2018)