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- A multi-omics strategy resolves the elusive nature of alkaloids in Podophyllum species. Joaquim V. Marques, Doralyn S. Dalisay, Hong Yang, Choonseok Lee, Laurence B. Davin, Norman G. Lewis
, Mol. BioSyst.
, 2014
, 10
, 2838
- Alkaloid formation through N-oxide intermediates; regioselective synthesis of (±)-corytuberine by redox reaction. Tetsuji Kametani, Masataka Ihara
, J. Chem. Soc., Perkin Trans. 1
, 1980
, 629
- CCXXXVII.—Synthetical experiments on the aporphine alkaloids. Part III. A synthesis of corytuberine dimethyl ether. John Masson Gulland, Robert Downs Haworth
, J. Chem. Soc.
, 1928
, 1834
- III.—The alkaloïds of Corydalis cava—corybulbine. James J. Dobbie, Alexander Lauder
, J. Chem. Soc., Trans.
, 1895
, 67
, 25
- XXXIII.—A new alkaloïd from Corydalis cava. James J. Dobbie, Alexander Lauder
, J. Chem. Soc., Trans.
, 1893
, 63
, 485
- β-Phenylethylamines and the isoquinoline alkaloids. K. W. Bentley
, Nat. Prod. Rep.
, 1989
, 6
, 405
- Organic chemistry
, J. Chem. Soc., Abstr.
, 1912
, 102
, i1
- Organic chemistry
, J. Chem. Soc., Abstr.
, 1911
, 100
, i937
- β-Phenylethylamines and the isoquinoline alkaloids. K. W. Bentley
, Nat. Prod. Rep.
, 1991
, 8
, 339
- Biosynthesis and synthetic biology of psychoactive natural products. Cooper S. Jamieson, Joshua Misa, Yi Tang, John M. Billingsley
, Chem. Soc. Rev.
, 2021
, 50
, 6950