ملخص
An efficient regio- and stereoselective method for the synthesis of cyclic trithiocarbonates on carbohydrate skeleton is described. A freshly prepared solution of sodium trithiocarbonate reacts with cis-oriented epoxytriflate pentoses 7-11 to yield the corresponding cyclic trithiocarbonates 12-16. Structures of all new compounds are established through MS, 1H and 13C NMR techniques.
اللغة الأصلية | English |
---|---|
الصفحات (من إلى) | 315-317 |
عدد الصفحات | 3 |
دورية | Tetrahedron Letters |
مستوى الصوت | 44 |
رقم الإصدار | 2 |
المعرِّفات الرقمية للأشياء | |
حالة النشر | Published - يناير 6 2003 |
منشور خارجيًا | نعم |
ASJC Scopus subject areas
- ???subjectarea.asjc.1300.1303???
- ???subjectarea.asjc.3000.3002???
- ???subjectarea.asjc.1600.1605???