85680-36-0Relevant articles and documents
Synthesis, molecular structure, conformation and biological activity of Ad-substituted N-aryl-tetraoxaspiroalkanes
Tyumkina, Tatyana V.,Makhmudiyarova, Nataliya N.,Kiyamutdinova, Guzeliya M.,Meshcheryakova, Ekaterina S.,Bikmukhametov, Kamil Sh.,Abdullin, Marat F.,Khalilov, Leonard M.,Ibragimov, Askhat G.,Dzhemilev, Usein M.
, p. 1749 - 1758 (2018/03/07)
An efficient method has been developed for the synthesis of 7′-arylspiro{adamantane-[2,3′]-(1′,2′,4′,5′,7′-tetraoxazocanes)} by the ring transformation reaction of spiro{adamantane-[2,3’]-(1′,2′,4′,5′,7′-pentaoxacane)} with arylamines in the presence of S
Synthesis of N-substituted 1,3,5-triazacyclohexanes catalyzed by starch sulfuric acid
Wu, Hui,Yuan, Rui,Wan, Yu,Yin, Wei,Pang, Li-Ling
experimental part, p. 1097 - 1102 (2012/03/11)
N-substituted 1,3,5-triazacyclohexanes were simply synthesized from the reaction of aromatic or fatty amines and formaldehyde catalyzed by recyclable starch sulfuric acid with good yields at room temperature.
Conformational Study of 1,3,5-Tris(o-methoxyphenyl)-1,3,5-triazacyclohexane and 1,3,5-Tris(p-methoxyphenyl)-1,3,5-triazacyclohexane
Adam, David,McCabe, Peter H.,Sim, George A.,Bouchemma, Ahcene
, p. 246 - 249 (2007/10/02)
The triazacyclohexane ring in both title compounds, C24H27N3O3 (1a) and C24H27N3O3 (1b), adopts a chair conformation with an equatorial-diaxial orientation of the aryl groups.The repulsion between axial groups is relieved by the displacement of the N-C(ar
