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- A new integrated method of magnetic separation of isoquinoline alkaloids from Coptis chinensis based on their magnetized derivatives and key physical properties. Lirong Nie, Xueting Feng, Hang Song, Zicheng Li, Shun Yao
, New J. Chem.
, 2020
, 44
, 7105
- Opium alkaloids. Part XVI. The biosynthesis of 1-benzylisoquinolines in Papaver somniferum. Preferred and secondary pathways; stereochemical aspects. Einar Brochmann-Hanssen, Chung-hsiung Chen, C. Rolland Chen, Hsüch-ching Chiang, Albert Y. Leung, Kenneth McMurtrey
, J. Chem. Soc., Perkin Trans. 1
, 1975
, 1531
- LXXXIX.—The resolution of tetrahydropapaverine into its optically active components. Constitution of papaverine. William Jackson Pope, Stanley John Peachey
, J. Chem. Soc., Trans.
, 1898
, 73
, 893
- XC.—The non-resolution of racemic tetrahydropapaverine by tartaric acid. William Jackson Pope, Stanley John Peachey
, J. Chem. Soc., Trans.
, 1898
, 73
, 902
- 281. Synthetic neuromuscular blocking agents. Part IV. Compounds related to both laudexium and suxamethonium. J. M. Z. Gladych, E. P. Taylor
, J. Chem. Soc.
, 1962
, 1481
- CLXXXII.—isoQuinoline derivatives. Part II. The constitution of the reduction products of papaverine. Frank Lee Pyman
, J. Chem. Soc., Trans.
, 1909
, 95
, 1610
- 697. Alkaloid biosynthesis. Part IV. 1-Benzylisoquinolines as precursors of thebaine, codeine, and morphine. A. R. Battersby, R. Binks, R. J. Francis, D. J. McCaldin, H. Ramuz
, J. Chem. Soc.
, 1964
, 3600
- Electrochemical oxidation of aromatic ethers. Part 8. Evidence of homogeneous electron transfer during the ‘low potential’ oxidation of laudanosine. Michael Hutchins, Malcolm Sainsbury, David I. C. Scopes
, J. Chem. Soc., Perkin Trans. 1
, 1983
, 2059
- 30. Synthetic neuromuscular blocking agents. Part II. Bis(quaternary ammonium salts) derived from laudanosine. E. P. Taylor
, J. Chem. Soc.
, 1952
, 142
- XIX.—isoQuinoline derivatives. Part VIII. The constitution of the reduction products of papaverine (continued). The constitution of pavine. Frank Lee Pyman
, J. Chem. Soc., Trans.
, 1915
, 107
, 176