Conformationally rigid analogs of aldose reductase inhibitor, tolrestat. Novel syntheses of naphthalene-fused .gamma.-, .delta.-, and .epsilon.-lactams
- 1 April 1990
- journal article
- research article
- Published by American Chemical Society (ACS) in The Journal of Organic Chemistry
- Vol. 55 (9) , 2694-2702
- https://doi.org/10.1021/jo00296a028
Abstract
No abstract availableThis publication has 4 references indexed in Scilit:
- Orally active aldose reductase inhibitors derived from bioisosteric substitutions on tolrestatJournal of Medicinal Chemistry, 1989
- Syntheses of 1-trifluoromethyl-2-naphthalenols via a novel construction of the naphthalene nucleusCanadian Journal of Chemistry, 1983
- PHARMACOPHORE REQUIREMENTS OF THE ALDOSE REDUCTASE INHIBITOR SITE1983
- Preparation of 4-aryl-1,2,3,4-tetrahydro-3,3-dimethylisoquinolines and 1,2,3,4-tetrahydro-3,3-dimethyl-4-phenylbenz[h]isoquinolinesJournal of Heterocyclic Chemistry, 1980