352000-78-3Relevant academic research and scientific papers
Lanthanide triflate catalyzed 1,3-dipolar cycloaddition reactions: Stereoselective synthesis of indenoisoxazolidines
Nugiel, David A.
, p. 3545 - 3547 (2001)
Substituted indenones reacted smoothly with a variety of in situ generated nitrones in the presence of lanthanide triflates to give exclusive exo 1,3-dipolar cycloaddition products in high yield. Judicious choice of the nitrone substituents allowed for further modification of the indenoisoxazolidine core to the corresponding indenoisoxazoline and indenoisoxazole analogs in high yield.
Efficient synthesis of 7-amino-3-hydroxyindan-1-one
Rajur, Raj,Rao, Venugopal N.,Kim, Hwa-Ok,Nagafuji, Pamela,Hearult, Xavier,Williams, John D.,Peet, Norton P.
experimental part, p. 626 - 635 (2009/08/15)
An efficient and reliable three-step synthesis of 7-amino-3-hydroxyindan-1- one (7) is described. Compound 7 is a versatile, three-dimensional, three-point scaffold that is useful for the construction of focused compound libraries. Copyright Taylor & Fran
