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Organozinc reagents, benzylic synthesis

Nickel-catalyzed enantioselective cross-couplings of racemic secondary benzylic halides with organozinc reagents have been further extended to the synthesis of chiral indanes. Indanes are useful building blocks for the synthesis of a variety of bioactive substances. For example, (/ )-3-ethylindanone 129 has been used for the preparation of the nonsteroidal androgen receptor agonist LG 121071. Fu and co-workers have reported on the rapid preparation... [Pg.383]

See other pages where Organozinc reagents, benzylic synthesis is mentioned: [Pg.305] [Pg.574] [Pg.57] [Pg.355] [Pg.355] [Pg.181] [Pg.103] [Pg.61] [Pg.104] [Pg.103] [Pg.209] [Pg.334] [Pg.392] [Pg.291] [Pg.341] [Pg.108] [Pg.273] [Pg.289] [Pg.299]

See also in sourсe #XX -- [ Pg.212 ]

See also in sourсe #XX -- [ Pg.212 ]

See also in sourсe #XX -- [ Pg.212 ]

See also in sourсe #XX -- [ Pg.212 ]

See also in sourсe #XX -- [ Pg.212 ]

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Benzyl reagent

Organozinc

Organozinc reagents

Organozinc reagents synthesis

Organozinc reagents, benzylic

Organozinc synthesis

Organozincates

Organozincs

Organozincs reagents