## Abstract The studied tetrahydroisoquinolines 1, 2 and 3 were synthesized from a common intermediate 6, which was prepared by addition of the lithium salt of dithiane 5 to hydrastinine chloride (4).
Total synthesis of kadsurenone and its analogs
✍ Scribed by M.M. Ponpipom; B.Z. Yue; R.L. Bugianesi; D.R. Brooker; M.N. Chang; T.Y. Shen
- Publisher
- Elsevier Science
- Year
- 1986
- Tongue
- French
- Weight
- 278 KB
- Volume
- 27
- Category
- Article
- ISSN
- 0040-4039
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✦ Synopsis
Kadsurenone, a specific receptor antagonist of platelet-activating factor and a natural product isolated from Piper futokadsura was prepared in three steps from 3,4-dimethoxycinnamyl alcohol and allyloxyphenol via rac_(2S,3S)-5-allyl-6-hydroxy-2_(3,4-dimethoxyphenyl)-3-methyl-2,3-dihydrobenzofuran. -
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