Synthesis and redox-enzyme modulation by amino-1,4-dihydro-benzo[d][1,2]dithiine derivatives
✍ Scribed by Sandraliz Espinosa; Melissa Solivan; Cornelis P. Vlaar
- Publisher
- Elsevier Science
- Year
- 2009
- Tongue
- French
- Weight
- 948 KB
- Volume
- 50
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
✦ Synopsis
A convenient method to prepare a series of benzodithiine derivatives was developed, via the synthesis of cyclic disulfide building blocks containing an amino-group linker. Some of the novel cyclic disulfide compounds are shown to modulate the activity of the redox-enzyme glutathione reductase.
📜 SIMILAR VOLUMES
## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable v
## Abstract 1‐Mono‐ and previously unknown 1,2‐disubstituted 1,2‐dihydro‐3,1‐benzoxazin‐4‐ones 7 and 9, potential prodrugs of flufenamic acid (6) and mefenamic acid (8), and 4__H__‐1,2‐dihydro‐pyrido‐[2,3‐__d__]‐[1,3]‐oxazin‐4‐ones 11, potential prodrugs of niflumic acid (10), were prepared; the st
## Abstract Two new structurally isomeric, 2‐(2,4,4‐trimethyl‐3,4‐dihydro‐2__H__‐benzo[__h__]chromen‐2‐yl)‐1‐naphthol (**1****)** and 3‐(2,4,4‐trimethyl‐3,4‐dihydro‐2__H__‐benzo[__g__]chromen‐2‐yl)‐2‐naphthol (**3**) have been synthesized from 2‐acetyl‐1‐naphthol and ethyl‐3‐hydroxy‐2‐naphthoate, r