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- Ergot alkaloids: synthetic approaches to lysergic acid and clavine alkaloids. Haichao Liu, Yanxing Jia
, Nat. Prod. Rep.
, 2017
, 34
, 411
- Ergot alkaloids: structure diversity, biosynthetic gene clusters and functional proof of biosynthetic genes. Christiane Wallwey, Shu-Ming Li
, Nat. Prod. Rep.
, 2011
, 28
, 496
- Chemistry of Indoles carrying a Basic Function. Part 5. Some Observations while Constructing an Ergoline Ring by Stobbe Reaction. István Moldvai, Eszter Temesvári-Major, Mihály Balázs, Eszter Gács-Baitz, Orsolya Egyed, Csaba Szántay
, J. Chem. Res. (S)
, 1999
, 687
- The structure of the ergot alkaloids. A. L. Glenn
, Q. Rev. Chem. Soc.
, 1954
, 8
, 192
- Biosynthesis of the ergot alkaloids. Dorota Jakubczyk, Johnathan Z. Cheng, Sarah E. O'Connor
, Nat. Prod. Rep.
, 2014
, 31
, 1328
- A novel electrochemical sensor for non-ergoline dopamine agonist pramipexole based on electrochemically reduced graphene oxide nanoribbons. Prashanth S. Narayana, Nagappa L. Teradal, J. Seetharamappa, Ashis K. Satpati
, Anal. Methods
, 2015
, 7
, 3912
- The synthesis of 9,10-dimethyl-4,6,6a,7,8,9,10,10a-octahydroindolo[3,4-gh]isoquinoline, the 8,9-dimethyl-8-aza analogue of ergoline. William H. Hunter, David E. Tupper
, J. Chem. Soc., Perkin Trans. 1
, 1987
, 707
- Synthetic entry into N(5)-ergolines. Jack E. Baldwin, Andrew K. Forrest, Sam Monaco, Robert J. Young
, J. Chem. Soc., Chem. Commun.
, 1985
, 1586
- The synthesis of 8-methyl-4,6,6a,7,8,9-hexahydroindolo[4,3-fg]isoquinoline, the 9,10-didehydro-7-methyl-7-aza analogue of ergoline. David C. Horwell, David E. Tupper, William H. Hunter
, J. Chem. Soc., Perkin Trans. 1
, 1983
, 1545
- Outlining migrainous through dihydroergotamine–serotonin receptor interactions using quantum biochemistry. José X. Lima Neto, Vanessa P. Soares-Rachetti, Eudenilson L. Albuquerque, Vinicius Manzoni, Umberto L. Fulco
, New J. Chem.
, 2018
, 42
, 2401