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Imines reaction with allyl organometallic compounds

Yamamoto and coworkers [3], however, have reported that reactions of al-lyl-9-BBN with certain chiral imines give the corresponding allylation products with very high enantiomeric excess, in essentially, the quantitative yields (Eq. 12.2). Table 12.1 summarizes these very high 1,2-asymmetric inductions. The main reason for poor selectivity of imine is the complex reactivity of imines toward other organometallic compounds [4-6]. [Pg.261]


See other pages where Imines reaction with allyl organometallic compounds is mentioned: [Pg.15]    [Pg.15]    [Pg.46]    [Pg.425]    [Pg.46]    [Pg.78]    [Pg.2]    [Pg.3]    [Pg.46]    [Pg.980]    [Pg.2]    [Pg.3]    [Pg.46]    [Pg.980]    [Pg.840]    [Pg.133]    [Pg.3]    [Pg.46]    [Pg.980]    [Pg.649]    [Pg.1336]    [Pg.2]    [Pg.247]    [Pg.216]   
See also in sourсe #XX -- [ Pg.2 ]




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Allyl compounds

Allyl organometallic compounds

Allyl organometallics

Allylations imines

Allylic compounds

Allylic organometallic compounds

Imine compounds

Imine reaction

Imines allylation

Imines allylation reactions

Imines compounds

Imines organometallics

Imines with organometallic

Imines, reactions

Organometallic compounds reaction

Organometallic compounds with

Reaction with imines

Reaction with organometallics

Reactions with organometallic compounds

With imines

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