934831-76-2Relevant academic research and scientific papers
Enantioselective synthesis of a potential key intermediate for the total synthesis of fumagillin
Ciampini, Marisa,Perlmutter, Patrick,Watson, Keith
, p. 243 - 250 (2007/10/03)
Key intermediate, 7, of a projected total synthesis of the anti-angiogenesis compound Fumagillin 1 and the semi-synthetic analogue TNP-470 2, has been prepared in enantiomerically pure form by employing an early nucleophilic addition ring closure [NARC] s
