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Claisen rearrangements charge-accelerated

Nubbemeyer U (2001) Synthesis of Medium-Sized Ring Lactams. 216 125-196 Nubbemeyer U (2005) Recent Advances in Charge-Accelerated Aza-Claisen Rearrangements. 244 149-213... [Pg.264]

Recent Advances in Charge-Accelerated Aza-Claisen Rearrangements... [Pg.149]

Keywords Aza-Claisen rearrangement 3-Aza-Cope rearrangement Chirality transfer Asymmetric induction Charge acceleration... [Pg.150]

Simple aromatic aza-Claisen rearrangement without charge acceleration by addition of an acid required other activating factors to enable the reaction to be run at acceptable temperatures. The reduction of ring strain was found to serve as a useful promoter to induce aromatic aza-Claisen rearrangement [21]. [Pg.165]

Nuhhemeyer, U. (2005) Recent advances in charge-accelerated aza-Claisen rearrangements. Top. Curr. Chem., 244, 149-213. [Pg.195]

See other pages where Claisen rearrangements charge-accelerated is mentioned: [Pg.151]    [Pg.611]    [Pg.461]    [Pg.1452]    [Pg.166]    [Pg.149]    [Pg.152]    [Pg.159]    [Pg.173]    [Pg.449]    [Pg.1140]    [Pg.356]    [Pg.197]    [Pg.107]   
See also in sourсe #XX -- [ Pg.847 , Pg.848 , Pg.849 ]

See also in sourсe #XX -- [ Pg.847 , Pg.848 , Pg.849 ]



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