329788-96-7Relevant articles and documents
Total synthesis of jadomycins B, S, T, and ILEVS1080
Yang, Xiaoyu,Yu, Biao
supporting information, p. 8431 - 8434 (2013/07/19)
Sweetening up jadomycin A: The first total synthesis of jadomycins B, S, T, and ILEVS1080 has been achieved, featuring construction of the unique 8H-benz[b]oxazolo[3,3-f]phenanthridine skeleton by biomimetic condensation of a quinone aldehyde with amino acid sodium salts and elaboration of the glycosides by Mitsunobu condensation (see figure). Copyright
Synthesis of benzo[b]phenanthridines and related naturally occurring 2-aryl-1,4-naphthoquinones by palladium- and copper-catalyzed coupling of organostannanes with bromoquinones
De Frutos, Oscar,Atienza, Carmen,Echavarren, Antonio M.
, p. 163 - 171 (2007/10/03)
Syntheses of phenanthroviridone, gilvocarcin BE-12406X2, antibiotic WS 5995B, and a key intermediate for the synthesis of jadomycin are described, based on palladium- and copper-catalyzed coupling reactions of sterically hindered arylstannanes