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Phosphines carbohydrate-functionalized

In numerous synthetic studies it has been demonstrated that DMP can be used for a selective oxidation of alcohols containing sensitive functional groups, such as unsaturated alcohols [297,1215-1218], carbohydrates and polyhydroxy derivatives [1216, 1219-1221], silyl ethers [1222,1223], amines and amides [1224-1227], various nucleoside derivatives [1228-1231], selenides [1232], tellurides [1233], phosphine oxides [1234], homoallylic and homopropargylic alcohols [1235], fluoroalcohols [1236-1239] and boronate esters [1240]. Several representative examples of these oxidations are shown below in Schemes 3.349-3.354. Specifically, the functionalized allylic alcohols 870, the Baylis-Hillman adducts of aryl aldehydes and alkyl acrylates, are efficiently oxidized with DMP to the corresponding a-methylene-p-keto esters 871 (Scheme 3.349) [1217]. The attempted Swern oxidation of the same adducts 870 resulted in substitution of the allylic hydroxyl group by chloride. [Pg.297]

Nickel-catalyzed ketone and aldehyde hydrosilylations have been developed with well-defined Ni(II) hydrides using phosphine anilide ligands (Scheme 3-84). This process is tolerant of a variety of functional groups including aryl halides. In mechanistically distinct processes, nickel(O) complexes of NHCs were shown to catalyze ketone hydrosilylations using carbohydrate-derived silanes in a process that allows reductive glycosylations of ketones. Chemoselectivity of the latter method was optimal in the presence of Ti(OR)4 additives. [Pg.396]

The compounds shown in Fig. 1.1 are hazardous to work with and require special procedures for their handling phosphine 1 is used in an industrial safety demonstration and the heterocyclic derivatives 2 and 3 [24] are extremely malodorous and sensitive to oxygen, igniting on the tip of a syringe whilst 4 is explosive [25]. For this reason, despite the fact that they are readily functionalized as a result of the two reactive P-H bonds, and have applications in fields as diverse as medicinal chemistry [3], polymer science [26, 27], carbohydrate modification [28] and macrocychc research [29], they remain underused and poorly understood as a compound class. [Pg.2]


See other pages where Phosphines carbohydrate-functionalized is mentioned: [Pg.641]    [Pg.973]    [Pg.120]    [Pg.346]    [Pg.2173]    [Pg.41]    [Pg.48]    [Pg.135]    [Pg.29]    [Pg.3230]    [Pg.544]    [Pg.71]    [Pg.13]   
See also in sourсe #XX -- [ Pg.149 ]




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Phosphines functionalized

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