73676-95-6Relevant articles and documents
Regularities of the amino-Claisen rearrangement mechanism
Abdrakhmanov,Borisov,Ismagilov,Nigmatullin,Khusnitdinov,Tolstikov
, p. 83 - 87 (2013/11/19)
The synthetic and kinetic regularities of the amino-Claisen rearrangement (ACR) were studied for the transformation of 2,5-dimethyl-N-(pent-3-en-2-yl) aniline. The ACR products are formed due to the conversion of a binary π-complex formed by the reaction of N-alkenylaniline hydrochloride with hydrochloride of the solvent (2,5-dimethylaniline).
CLAISEN REARRANGEMENT OF STERICALLY HINDERED N-ALKENYLINDOLINES
Abdrakhmanov, I. B.,Mustafin, A. G.,Tolstikov, G. A.,Spirikhin, L. V.,Khalikov, L. M.
, p. 561 - 565 (2007/10/02)
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