ChemInform Abstract: A Synthetic Approach to Methyl Thieno[2,3-d][1,2,3]thiadiazole Carboxylates via Diazotation.
β Scribed by Peter Stanetty; Marko D. Mihovilovic
- Publisher
- John Wiley and Sons
- Year
- 2010
- Weight
- 30 KB
- Volume
- 30
- Category
- Article
- ISSN
- 0931-7597
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β¦ Synopsis
A Synthetic Approach to Methyl Thieno [2,3-d][1,2,3]thiadiazole Carboxylates via Diazotation.
-A route to title compounds (VII) as highly potent inducers of systemic acquired resistance is reported. Cyclization towards the thiadiazole ring system is carried out using diazotation techniques. An alternative approach via nitration of the benzylthio-substituted thiophene (VIII) only gives the sulfur-oxidized product (IX).
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## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a βFull Textβ option. The original article is trackable v
## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a βFull Textβ option. The original article is trackable v
Synthesis of Thieno[2,3d] [1,2,3]thiadiazole-6-carboxylic Acid Derivatives via Hurd-Mori Cyclization. -A short and efficient procedure for the large-scale synthesis of the title compound (VIII) from cheap and readily available diacid (I) and thioacetic acid is reported. A modified mechanism for the