Synthesis of Novel trans-4-(Substituted-benzamido)-3,4-dihydro-2H-benzo[b]pyran-3-ol Derivatives as Potential Anticonvulsant Agents with a Distinctive Binding Profile
- 1 January 1996
- journal article
- letter
- Published by American Chemical Society (ACS) in Journal of Medicinal Chemistry
- Vol. 39 (23) , 4537-4539
- https://doi.org/10.1021/jm960535w
Abstract
No abstract availableThis publication has 7 references indexed in Scilit:
- Potassium Channels And Their ModulatorsPublished by Taylor & Francis ,1996
- Stereochemical preferences and requirement for the 3-hydroxyl group in novel anticonvulsant 4-fluorobenzoylamino benzopyransBioorganic & Medicinal Chemistry Letters, 1995
- Mechanisms of action of new antiepileptic drugs: rational design and serendipitous findingsTrends in Pharmacological Sciences, 1994
- Enantioselective catalytic epoxidation of cinnamate estersTetrahedron, 1994
- Rational design of Mn-salen catalyst (2): Highly enantioselective epoxidation of conjugated cis olefinsTetrahedron, 1994
- Synthesis and antihypertensive activity of 4-(substituted-carbonylamino)-2H-1-benzopyransJournal of Medicinal Chemistry, 1990
- Synthesis and antihypertensive activity of 4-(cyclic amido)-2H-1-benzopyransJournal of Medicinal Chemistry, 1986