685077-49-0Relevant articles and documents
Taxane diterpene synthesis studies. Part 2: Towards taxinine - enantiospecific construction of an AB-ring substructure incorporating both quaternary carbon centres and attempts to annulate the C-ring
Banwell, Martin G.,McLeod, Malcolm D.,Riches, Andrew G.
, p. 53 - 66 (2007/10/03)
In connection with efforts to develop an efficient total synthesis of the biologically active natural product taxinine 1, the enzymatically-derived and monochiral cis-1,2-dihydrocatechol 7 was converted, over several steps including a Diels-Alder cycloadd