478314-18-0Relevant articles and documents
Total synthesis and absolute configuration of marine bisnor-diterpenoid elisabethin C
Miyaoka, Hiroaki,Honda, Daichi,Mitome, Hidemichi,Yamada, Yasuji
, p. 7773 - 7775 (2007/10/03)
Total synthesis of marine bisnor-diterpenoid elisabethin C was successfully carried out by stereoselective construction of bicyclo[4.3.0]nonane ring system with Dieckmann cyclization as the key step. The absolute configuration of elisabethin C was determined based on this total synthesis.