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Silylformylation epoxides

Silylformylation, defined as the addition of RsSi- and -CHO across various types of bonds using a silane R3SiH, CO, and a transition metal catalyst, was discovered by Murai and co-workers, who developed the Co2(CO)8-catalyzed silylformylation of aldehydes, epoxides, and cyclic ethers [26]. More recently, as described in detail in Section 5.3.1, below, alkynes and alkenes have been successfully developed as silylformylation substrates. These reactions represent a powerful variation on hydroformylation, in that a C-Si bond is produced instead of a C-H bond. Given that C-Si groups are subject to, among other reactions, oxidation to C-OH groups, silylformylation could represent an oxidative carbonylation of the type described in Scheme 5.1. [Pg.103]

In sharp contrast to silylformylation of alkynes, specific combination [Rh(GOD)Gl]2/THF of catalyst precursor and solvent is quite important for selective silylformylation of aldehydes. Go-use of A-methylpyrazole is crucial to perform silylformylation of epoxides ( [Rh(GO)2Gl]/GH2Cl2 " and oxetanes [Rh(GO)2Gl]2/toluene. ... [Pg.475]

Ring-opening silylformylation has been observed by Murai and coworkers in reactions of cyclic ethers. When the cobalt complex Co2(CO)8 is used as the catalyst in reactions of epoxides, an excess of substrate is required to prevent further reaction of the product siloxy aldehyde.1192 Further investigation led to the discovery of [RhCl(CO)2]2/l-methyl-pyrazole as an effective catalyst combination for the reaction of oxi-ranes119b and oxetanes.J19c For example, oxetane undergoes silylformylation to give 4-(dimethylphenylsiloxy)butanal in 81% yield [Eq. (45)]. [Pg.236]

Rh catalyses the hydrosilylation of alkenes and the dehydrogenative silylation of 1,5-dienes and alkynes, and the silylcarbonylation of alkynes to give p-silylacrylaldehydes with exceptional stereocontrol , ketones and enones give silyl enol ethers, 1,3-cyclobutane dione gives 3-hydroxycyclobutanone, and assists in the silylformylation of ethynyl pyirolidone derivatives to give pyrrolizidine alkaloids, and epoxides to give p-siloxy aldehydes, and... [Pg.98]


See other pages where Silylformylation epoxides is mentioned: [Pg.239]    [Pg.473]    [Pg.488]    [Pg.489]    [Pg.490]    [Pg.1772]    [Pg.234]    [Pg.615]    [Pg.302]   
See also in sourсe #XX -- [ Pg.11 ]




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Silylformylation

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