79249-72-2Relevant academic research and scientific papers
Base Catalysed Rearrangements involving Ylide Intermediates. Part 13. Further Rearrangements of 2-Oxidoanilinium Ylides
Ollis, W. David,Somanathan, Ratnasamy,Sutherland, Ian O.
, p. 2930 - 2942 (2007/10/02)
The 2-oxidoanilinium ylides (7) rearrange on heating to give the ethers (10) together with the dienones (8) and the phenols (11) for cases where the aromatic ring has a 5-alkyl substituent or a mixture of the dienones (8) and (12) for cases where the aromatic ring is 3,5-disubstituted.A study of the deuteriated ylides (25) shows that these reactions involve competing concerted and radical-pair processes.The base-catalysed rearrangements of the 2-hydroxy-N-pentadienylanilinium salts (33) give the ethers (34) and the phenols (35): these products result from competing concerted and rearrangements of the ylides (36) corresponding to the salts (33).
The Role of Cyclohexadienones in the Thermal Sigmatropic Rearrangements of 2-Oxidoanilinium Ylides
Ollis, W. David,Somanathan, Ratnasamy,Sutherland, Ian O.
, p. 573 - 575 (2007/10/02)
Thermal isomerization of N-allyl-2-oxidoanilinium ylides under mild conditions yields three products which are each formed by two types of competitive pathways; the minor pathway involves a radical pair intermediate and three modes of coupling, and the ma
