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Total synthesis and absolute configuration of marine bisnor-diterpenoid elisabethin C

✍ Scribed by Hiroaki Miyaoka; Daichi Honda; Hidemichi Mitome; Yasuji Yamada

Publisher
Elsevier Science
Year
2002
Tongue
French
Weight
203 KB
Volume
43
Category
Article
ISSN
0040-4039

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✦ Synopsis

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.

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