Water enabled, nickel-catalyzed highly chemoselective C-allylation of (NH)-indoles employing alcohols.

The first 'in-water' nickel-catalyzed chemoselective C3-allylation of (NH)-indoles employing allylic alcohols under mild conditions is reported here. Different indoles and allylic alcohols were found compatible with excellent chemo- (C vs. N: >99%; C2vs. C3: >98%), regio- (linear vs. branch: >99%), and stereo-selectivity (E vs. Z: >99%) and functional group tolerance. The use of water not only provides sustainability by eliminating the need for organic solvent as reaction media but it also activates allylic alcohols via hydrogen bond networking and stabilizes the consequent hydroxide ion (strong solvation effect) resulting in facile oxidative addition, and thereof the formation of electrophilic π-allylNi complexes leading to C3-allyl indoles. The study further highlights the first Hydrogen-bond assisted intermolecular N → C allylic migration via π-allylNi complexation and reports the first synthesis of allyl indoles using allylamine as electrophilic precursors. [ABSTRACT FROM AUTHOR]