Regioselectivity in the acid-catalyzed isomerization of 2-substituted 1, 4-dihydro-1, 4-epoxynaphthalenes
DG Batt, DG Jones, S La Greca
Index: Batt, Douglas G.; Jones, David G.; Greca, Susan La Journal of Organic Chemistry, 1991 , vol. 56, # 23 p. 6704 - 6708
Full Text: HTML
Citation Number: 40
Abstract
In the course of examining the structure-activity relationships of a series of 5-lipoxygenase- inhibitory 2-(arylmethyl)-1-naphthols,'we wanted to prepare 8-substituted analogues, hoping that greater metabolic stability would result from steric hinderance near the hydroxyl group. Synthetic approaches involving elaboration of preexisting 2-or 8-substituted naphthols were excluded because of potential difficulties arising from peri interactions, which can induce ...
Related Articles:
[Stoner, Eric J.; Cothron, Darlene A.; Balmer, Mary K.; Roden, Brian A. Tetrahedron, 1995 , vol. 51, # 41 p. 11043 - 11062]
[Craig, Donald; Etheridge, Christopher J. Tetrahedron, 1996 , vol. 52, # 48 p. 15289 - 15310]
[Craig, Donald; Etheridge, Christopher J. Tetrahedron, 1996 , vol. 52, # 48 p. 15289 - 15310]
[Stoner, Eric J.; Cothron, Darlene A.; Balmer, Mary K.; Roden, Brian A. Tetrahedron, 1995 , vol. 51, # 41 p. 11043 - 11062]