308086-53-5Relevant academic research and scientific papers
Synthesis of conformationally constrained spirohydantoins with a dibenzo[a,d]heptadiene ring
Tao,Timberlake
, p. 1449 - 1453 (2007/10/03)
Conformationally constrained dibenzo[a,d]cycloheptadiene-based spirohydantoins were prepared from dibenzosuberone via the transformation of the α-hydroxy ester to the azido ester, followed by its reduction to the amino ester, and cyclization of the carbomethoxy N,N'-asymmetric ureas, derived from the amino ester with triphosgene and a variety of amines. A novel ring expansion reaction was also observed in the process.
