863423-85-2Relevant academic research and scientific papers
Regio- and stereocontrolled total synthesis of benanomicin B
Ohmori, Ken,Tamiya, Minoru,Kitamura, Mitsuru,Kato, Hirohisa,Oorui, Mami,Suzuki, Keisuke
, p. 3871 - 3874 (2007/10/03)
(Chemical Equation Presented) Fully controlled total synthesis of benanomicin B was achieved by exploiting two key steps : a stereocontrolled ring-opening of a lactone (see scheme, step A), and a semipinacol cyclization of an acetal-aldehyde derivative discriminating the two hydroxy groups of the pseudo-C2-symmetric 1,2-diol moiety (step B).
