Synthesis of N-substituted 1,2,5-thiadiazolidine and 1,2,6-thiadiazinane 1,1-dioxides from primary amines
โ Scribed by Paul D. Johnson; Sarah A. Jewell; Donna L. Romero
- Publisher
- Elsevier Science
- Year
- 2003
- Tongue
- French
- Weight
- 147 KB
- Volume
- 44
- Category
- Article
- ISSN
- 0040-4039
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โฆ Synopsis
Alkyl and aryl N-substituted 1,2,5-thiadiazolidine and 1,2,6-thiadiazinane 1,1-dioxides 6 were synthesized in good yields from the reaction of sulfuryl chloride with 2-chloroethylamine or 3-chloropropylamine hydrochlorides, respectively, followed by treatment with a primary amine and triethylamine, and ring closure with K 2 CO 3 in DMSO.
๐ 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, please click on HTML or PDF.
A sulfahydantoin (3-oxo-1,2,5-thiadiazolidine 1,1-dioxides) absolute configuration of the chiral centers for the derivative L-Phe-D-Ala, a congener of the series, was established by X-motif is used as a new type of peptidic constraint to lock two consecutive amide nitrogens by a sulfonyl bridge. The