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Binaphthyl phosphines

Hayashi showed that binaphthyl phosphine oxides such as 193 undergo phosphorus-lithium exchange with BuLi to generate binaphthylllithiums such as 194.162... [Pg.142]

R)-2-DIPHENYLPHOSPHINO-2 -METHOXY-1,1 -BINAPHTHYL (Phosphine, (2 -methoxy[1,1l-binaphthaien]-2-yl)diphenyl-, (R)-)... [Pg.146]

The asymmetric hydrosilylation of 1-alkenes giving highly optically active 2-tri-chlorosilylalkanes is catalyzed by palladium complexes with chiral monodentate binaphthyl phosphine (MOP) ligands. ... [Pg.320]

This research group also investigated the intramolecular arene epoxidation of binaphthyl phosphine derivatives. Singlet oxygen reacts with l,l -binaphthyl-2-di-tert-butylphosphine to form the corresponding phosphine oxide-epoxide intermediate with complete retention of stereochemistry. This then undergoes a slow NIH-rearrangement to form the 1-phosphinoxido-l -hydroxy binaphthyl derivative (Scheme 9). °... [Pg.74]

In the course of developing an easy access to chiral y-butenolides, Shi et al. have established an efficient multifunctional chiral binaphthyl phosphine-catalysed allylic substitution of Morita-Baylis-Hillman acetate with 2-tri-methylsiloxy furan. The regjospecific allylic substitution occurred to provide the xyra-y-butenolide in good to excellent yield, high regjoselectivity and excellent enantioselectivity by using water as an additive. The scope of this reaction could be successfully extended to a variety of Morita Baylis Hillman acetates, as shown in Scheme 5.10. [Pg.164]


See other pages where Binaphthyl phosphines is mentioned: [Pg.143]    [Pg.196]    [Pg.11]    [Pg.13]    [Pg.499]    [Pg.153]    [Pg.192]    [Pg.282]    [Pg.138]    [Pg.178]    [Pg.85]    [Pg.13]    [Pg.313]    [Pg.313]    [Pg.153]    [Pg.986]   


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Binaphthyl phosphine reaction with

Binaphthyls

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