Ruthenium-catalysed C–H/C–N bond activation: facile access to isoindolinones
A facile ruthenium-catalysed C–H/C–N bond activation and the subsequent annulation of readily available benzoic acids with in situ generated formaldimines are developed for the efficient synthesis of a wide range of biologically important isoindolinones.
1978 ◽
Vol 36
(1)
◽
pp. 68-69
1992 ◽
Vol 57
(1)
◽
pp. 194-203
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