Total synthesis and absolute configuration of marine bisnor-diterpenoid elisabethin C
Author/Authors :
Miyaoka، نويسنده , , Hiroaki and Honda، نويسنده , , Daichi and Mitome، نويسنده , , Hidemichi and Yamada، نويسنده , , Yasuji، نويسنده ,
Issue Information :
هفته نامه با شماره پیاپی سال 2002
Pages :
3
From page :
7773
To page :
7775
Abstract :
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.
Keywords :
Biologically active compounds , terpenes and terpenoids , Marine metabolites
