Streamlined Stereoselective Entry to (−)-Quinagolide and to 3-Substituted Octahydrobenzo[g]-Quinolines
Author:
Affiliation:
1. Department of Pharmacy, University of Pisa, Via Bonanno 33, 56126 Pisa, Italy
2. Chemical Development, Global Pharmaceutical R&D, Ferring Pharmaceuticals A/S, Amager Strandvej 405, DK 2770 Kastrup, Denmark
Funder
Ferring
Publisher
American Chemical Society (ACS)
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.joc.3c02681
Reference22 articles.
1. Octahydrobenzo[g]quinolines: potent dopamine agonists which show the relationship between ergolines and apomorphine
2. P-Dimethoxy-substituted trans-octahydrobenzo[f]- and -[g]quinolines: synthesis and assessment of dopaminergic agonist effects
3. N-(Iodopropenyl)-octahydrobenzo[f]- and -[g]quinolines: Synthesis and Adrenergic and Dopaminergic Activity Studies
4. A New Practical Route for the Manufacture of (4aR,10aR)-9-Methoxy-1-methyl-6-trimethylsilanyl- 1,2,3,4,4a,5,10,10a-octahydrobenzo[g]quinoline
5. Synthesis of the Dopamine Agonist (-)-Quinpirole
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