678149-59-2Relevant academic research and scientific papers
Total synthesis of enokipodins A-D and cuparene-1 ,4-diol
Srikrishna,Rao, M. Srinivasa
experimental part, p. 1363 - 1371 (2011/01/13)
A Claisen rearrangement and RCM reaction based sequence has been developed for total synthesis of the antifungal sesquiterpenes enokipodins A-D and cuparene-1 ,4-diol starting from 2,5-dimethoxy-4-methythydroquinone. Copyright
The First Total Synthesis of the Antimicrobial Sesquiterpenes (±)-Enokipodins A and B
Srikrishna,Rao, M. Srinivasa
, p. 374 - 376 (2007/10/03)
Efficient first total synthesis of antimicrobial sesquiterpenes enokipodins A and B (1 and 2, respectively) and formal total synthesis of cuparene-1,4-diol (5) and cuparene-1,4-quinone (7) have been accomplished starting from 2,5-dimethoxy-4-methyl-acetop
