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Brown and coworkers [1] have reported that lithiumB-iso-2-ethylapopinocam-pheyl-9-borabicyclo[3.3.1]nonyl hydride (Eapine-Flydride), prepared by hy-droboration of 2-ethylapopinene with 9-BBN followed by treatment with tert-butyllithium, is as effective as NB-Enantride for the chiral reduction of prochiral ketones (Scheme 26.6 Table 26.21) [1]. [Pg.461]

See other pages where Eapine-hydride is mentioned: [Pg.195] [Pg.1] [Pg.461] [Pg.461] [Pg.462] [Pg.195] [Pg.1] [Pg.461] [Pg.461] [Pg.462]