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Catalytic Asymmetric Total Synthesis of (+)- and (-)-Paeoveitol via a Hetero-Diels-Alder Reaction.

Tian-Ze LiChang-An GengXiu-Juan YinTong-Hua YangXing-Long ChenXiao-Yan HuangYun-Bao MaXue-Mei ZhangJi-Jun Chen
Published in: Organic letters (2017)
The first catalytic asymmetric total synthesis of (+)- and (-)-paeoveitol has been accomplished in 42% overall yield via a biomimetic hetero-Diels-Alder reaction. The chiral phosphoric acid catalyzed hetero-Diels-Alder reaction showed excellent diastereo- and enantioselectivity (>99:1 dr and 90% ee); two rings and three stereocenters were constructed in a single step to produce (-)-paeoveitol on a scale of 452 mg. This strategy enabled us to selectively synthesize both paeoveitol enantiomers from the same substrates by simply changing the enantiomer of the catalyst.
Keyphrases
  • room temperature
  • ionic liquid
  • electron transfer
  • crystal structure