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Isolation and Bioinspired Total Synthesis of Rugosiformisin A, A Skeleton-Rearranged Abietane-Type Diterpenoid from Isodon rugosiformis .

Bin WangHua-Yi JiangJin YangJun LiBing-Chao YanXi ChenKun HuXing-Ren LiHan-Dong SunJun DengPema-Tenzin Puno
Published in: Organic letters (2022)
Rugosiformisin A, a skeleton-rearranged abietane-type diterpenoid with a spiro[4.5]decane motif, was isolated from Isodon rugosiformis . Its structure was unambiguously established via NMR spectroscopic analysis and single-crystal X-ray diffraction. A bioinspired asymmetric synthesis of rugosiformisin A was achieved in 15 steps with 2.7% overall yield. The synthesis features an iridium-catalyzed asymmetric polyene cyclization and a semipinacol rearrangement.
Keyphrases
  • solid state
  • high resolution
  • magnetic resonance
  • room temperature
  • electron microscopy
  • computed tomography
  • magnetic resonance imaging
  • dual energy
  • crystal structure
  • molecular dynamics simulations