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Hydrozirconation and Further Transmetalation Reactions

Bruce H. Lipshutz, Steven S. Pfeiffer, Kevin Noson, and Takashi Tomioka [Pg.110]

Patterns for addition of the Schwartz reagent to multiple C—C bonds in terms of regio-and stereochemistry are well-established for most substituents, as is the fundamental chemistry of the newly formed Csp2—Zr and Csp3—Zr bonds. Conversion to halides and [Pg.110]

Reduction of a tertiary amide with the Schwartz reagent. [Pg.111]

Lipshutz, B. H., Pfeiffer, S. S., Noson, K., Tomioka, T. Hydrozirconation and further transmetalation reactions. Titanium and Zirconium in... [Pg.671]

See other pages where Hydrozirconation and Further Transmetalation Reactions is mentioned: [Pg.110] [Pg.111] [Pg.113] [Pg.115] [Pg.117] [Pg.119] [Pg.125] [Pg.127] [Pg.129] [Pg.131] [Pg.133] [Pg.135] [Pg.137] [Pg.139] [Pg.141] [Pg.143] [Pg.145] [Pg.147] [Pg.110] [Pg.111] [Pg.113] [Pg.115] [Pg.117] [Pg.119] [Pg.121] [Pg.123] [Pg.125] [Pg.127] [Pg.129] [Pg.131] [Pg.133] [Pg.135] [Pg.137] [Pg.139] [Pg.141] [Pg.143] [Pg.145] [Pg.147]

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And transmetallation

Hydrozirconation

Transmetalation

Transmetalations

Transmetallation

Transmetallation reactions

Transmetallations