Synthesis of 2-phenyl-4,5,6,7-tetrahydro-1H-indoles with a chiral substituent at the nitrogen atom
An efficient method has been developed for the enantioselective synthesis of 2-phenyl-4,5,6,7-tetra-hydro-1H-indoles containing chiral substituents at the nitrogen atom. It is based on opening of the epoxide fragment of 1-phenylethynyl-7-oxabicyclo[4.1.0]
Andreev, I. A.,Ryzhkov, I. O.,Kurkin, A. V.,Yurovskaya, M. A.
p. 715 - 719,5
(2020/09/09)
More Articles about upstream products of 1401465-26-6