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Cp2Zr Cl

RCH2CH[B(OR)2]ZiClCp2, cat CuBr-SMe2 Cp2Zr(Cl)CH=CHR, cat CuOTf, Lil Cp2MeZrCH=CHR / Me2Cu(CN)Li2... [Pg.1602]

RC=CCH2OTf Cp2Zr(Cl)CH=CHR/MeLi/ cat Me2Cu(CN)Li2 /Me3ZnLi JACS 116 11689 (1994)... [Pg.1609]

The use of Cp2Zr(Cl)BH4 [prepared by the action of BH3 MezS on CpaZriHlCl (98) or by treating Cp ZrCU with 1 mole equivalent of LiBH4 (73)] as a selective reducing agent for converting aldehydes or ketones to alcohols has also been recently exploited (98). [Pg.292]

SCHWARTZ Hydrozirconation Hydroafconation wWi Cp2Zr(Cl)H and Michael addition of the Zr reagent... [Pg.403]

Continuing studies of the hydrozirconation system Cp2Zr(Cl)H illustrate its versatility. For example, chloro-olefins such as 4-chlorocyclohexane react to give moderate yields of bicyclo[3,l,0]hexane. Ring formation is believed to occur via Zr—X y-elimination. y5-Unsaturated aldehydes and halides have been obtained from CO insertion into the Zr—C bonds of intermediates obtained from 1,3-dienes and Cp2Zr(Cl)H.3 ... [Pg.39]

See other pages where Cp2Zr Cl is mentioned: [Pg.284]    [Pg.140]    [Pg.50]    [Pg.159]    [Pg.96]    [Pg.243]    [Pg.304]    [Pg.321]    [Pg.1602]    [Pg.1602]    [Pg.1602]    [Pg.1602]    [Pg.1602]    [Pg.1610]    [Pg.292]    [Pg.47]    [Pg.44]    [Pg.530]    [Pg.530]    [Pg.530]    [Pg.1266]    [Pg.1266]    [Pg.46]    [Pg.1602]    [Pg.1602]    [Pg.1602]    [Pg.1602]    [Pg.1602]    [Pg.1602]    [Pg.1610]    [Pg.69]    [Pg.1266]    [Pg.1266]    [Pg.336]    [Pg.29]    [Pg.746]    [Pg.884]    [Pg.907]    [Pg.911]    [Pg.912]    [Pg.917]    [Pg.923]    [Pg.976]    [Pg.96]    [Pg.243]   
See also in sourсe #XX -- [ Pg.192 ]

See also in sourсe #XX -- [ Pg.368 ]

See also in sourсe #XX -- [ Pg.138 , Pg.196 ]



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Cp2Zr

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