A new synthesis of 2-amino-6-7-dihydroxy tetrahydronaphthalene (ADTN) via functionalized aryl-lithium reagents and methyl 2-trimethylsilylacrylate - a new annulation sequence
- 31 December 1981
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 22 (38) , 3707-3710
- https://doi.org/10.1016/s0040-4039(01)81999-7
Abstract
No abstract availableKeywords
This publication has 23 references indexed in Scilit:
- Six-membered-ring annulation via a conjugate addition-alkylation sequence using functionalized aryllithium reagents and vinyl sulfonesThe Journal of Organic Chemistry, 1981
- 2-Amino-6,7-dihydroxytetrahydronaphthalene and the receptor-site preferred conformation of dopamine—a commentaryJournal of Pharmacy and Pharmacology, 1980
- Elevation of brain neuroleptic/dopamine receptors in schizophreniaAmerican Journal of Psychiatry, 1980
- At Issue: An Un-Dopamine Hypothesis of SchizophreniaSchizophrenia Bulletin, 1980
- AN EFFICIENT SYNTHESIS OF 4,5-DIMETHOXYBENZOCYCLOBUTENEviaTHE PARHAM CYCLIALKYLATION REACTIONOrganic Preparations and Procedures International, 1978
- Facile syntheses of potent dopaminergic agonists and their effects on neurotransmitter releaseJournal of Medicinal Chemistry, 1978
- Effects of some derivatives of 2-aminotetralin on dopamine-sensitive adenylate cyclase and on the binding of [3H]haloperidol to neuro-leptic receptors in the rat striatumBiochemical Pharmacology, 1978
- Cerebral dopamine agonist properties of some 2-aminotetralin derivatives after peripheral and intracerebral administrationJournal of Medicinal Chemistry, 1977
- Functionalized aryllithium intermediates a new route to 3,4-dihydroisoquinolines.Tetrahedron Letters, 1977
- Derivatives of 2-aminoetetralinJournal of the Chemical Society C: Organic, 1967