1,4-Diarylbutanes undergo intramolecular oxidation with vanadium oxytrifluoride to yield dibenzo[a, c]cyclooctenes. Two short synthetic routes to the lignan, (±)-deoxyschizandrin have been developed from 3,4,5-trimethoxypropiophenone.
Synthesis of diarylbutanes from cordigerines and reinvestigation of their oxidative couplings in deoxyschizandrins. - An unusual formation of phenyltetralin lignans -
作者:Y. Landais、A. Lebrun、V. Lenain、J.-P. Robin
DOI:10.1016/s0040-4039(00)95617-x
日期:——
Dibenzylbutanolide lignans including cordigerines were synthetized and transformed in the corresponding diarylbutane lignans which were submitted to non-phenolic oxidativecoupling conditions by using RuO2 or Tl2O3 in trifluoroacetic medium to give deoxyschizandrins. A concurrently aryl-benzylcoupling leads to the formation of the corresponding phenyltetralin of which the structure was confirmed by
通过在三氟乙酸介质中使用RuO 2或Tl 2 O 3合成包括相应的二芳基丁烷木脂素在内的二苄基丁醇木脂素并在相应的二芳基丁烷木脂素中转化,将其转化为非酚类氧化偶联条件。同时发生的芳基-苄基偶联导致形成相应的苯基四氢萘,其结构已通过全合成得到证实。
Ruthenium dioxide in fluoro acid medium V. Application to the non phenolic oxidative coupling of diarylbutanes. Conformational studies of and deoxyschizandrins.
作者:R. Dhal、Y. Landais、A. Lebrun、V. Lenain、J.-P. Robin
DOI:10.1016/s0040-4020(01)80826-7
日期:1994.1
Ruthenium (IV) dioxide dihydrate in fluoro acidic medium was found to be a very efficient agent for the non phenolic oxidativecoupling of diarylbutanes. We observed along with the expected aryl-aryl coupling, an unusual aryl-benzylcoupling, leading to a known class of lignans, the aryltetralins. Conformational studies of resultant and deoxyschizandrins were performed using high resolution NMR and
Highly Selective Formation of Eight-Membered-Ring Systems by Oxidative Cyclization with Molybdenum PentachlorideâAn Environmentally Friendly and Inexpensive Access to 2,2â²-Cyclolignans The work was supported by the Deutschen Forschungsgemeinschaft and H. C. Starck (Goslar, Germany) by a donation of MoCl5. We particularly thank Prof. Dr. Dieter Hoppe for fruitful discussions and support in this project.
作者:Beate Kramer、Anne Averhoff、Siegfried R. Waldvogel