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2- - 1 -alkoxy- 1-silyloxy-1 -alkene

Alkyl and silyl nitronates are, in principle, /V-alkoxy and /V-silyloxynitrones, and they can react with alkenes in 1,3-dipolar cycloadditions to form /V-alkoxy- or /V-silyloxyisoxaz.olidine (see Scheme 8.25). The alkoxy and silyloxy groups can be eliminated from the adduct on heating or by acid treatment to form 2-isoxazolines. It should be noticed that isoxazolines are also obtained by the reaction of nitrile oxides with alkenes thus, nitronates can be considered as synthetic equivalents of nitrile oxides. Since the pioneering work by Torssell et al. on the development of silyl nitronates, this type of reaction has become a useful synthetic tool. Recent development for generation of cyclic nitronates by hetero Diels-Alder reactions of nitroalkenes is discussed in Section 8.3. [Pg.267]


See other pages where 2- - 1 -alkoxy- 1-silyloxy-1 -alkene is mentioned: [Pg.2153]    [Pg.2155]    [Pg.2155]    [Pg.2156]    [Pg.2181]    [Pg.2182]    [Pg.2014]    [Pg.2153]    [Pg.2155]    [Pg.2156]    [Pg.2182]    [Pg.1029]    [Pg.1078]    [Pg.2398]    [Pg.2410]    [Pg.75]    [Pg.267]    [Pg.398]    [Pg.2001]    [Pg.2005]    [Pg.2013]    [Pg.2044]    [Pg.2044]    [Pg.2057]    [Pg.2061]    [Pg.2099]    [Pg.2099]    [Pg.2101]    [Pg.2104]    [Pg.2104]    [Pg.2107]    [Pg.2112]    [Pg.2143]    [Pg.2146]    [Pg.2146]    [Pg.2149]    [Pg.2149]    [Pg.2150]    [Pg.2157]    [Pg.2158]    [Pg.2158]    [Pg.2165]    [Pg.2168]    [Pg.2168]   
See also in sourсe #XX -- [ Pg.1746 ]




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1 - -1- 1 -silyloxy-1 -alkene

2- alkanoate ester 1 -alkoxy-1 -silyloxy-1 -alkene

5- silyloxy-1-alkene 4-alken

Alkenes alkoxy

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