## 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 “Full Text” option. The original article is trackable v
Stereoselective synthesis of s-(2-deoxy-α-D-glycosyl)- phosphorodithioates1 and of their (2R)-2-deoxy-2-deuterio- analogues. Novel route to C-2 d
✍ Scribed by Joanna Borowiecka; Paweł Lipka; Maria Michalska
- Publisher
- Elsevier Science
- Year
- 1988
- Tongue
- French
- Weight
- 623 KB
- Volume
- 44
- Category
- Article
- ISSN
- 0040-4020
No coin nor oath required. For personal study only.
✦ Synopsis
Addition oP C,F'-dialkylphosphorodithioic acids to fully protected 1,2-unsaturated hsxo-and pentopyranoses gives S-(2-deoxy-glycosyl)-phosphorodithioates 'P -OH RO' 'SH -# H /OR HS-l'OR 2 2 Scheme I 2oa the &_-adducte. The observed Oc'/s ratio was 89:ll and 92:8, respectively. pllso in these cases isolation oP the &-isomers 3f and 3 was readily accomplished by crystallization.
📜 SIMILAR VOLUMES
## Abstract The 1,3,4,6‐tetra‐__O__‐acetyl‐2‐azido‐2‐deoxy‐__β__‐D‐mannopyranose (**4**) or the mixture of 1,3,6‐tri‐__O__‐acetyl‐2‐azido‐2‐deoxy‐4‐__O__‐(2,3,4,6‐tetra‐__O__‐acetyl‐__β__‐D‐galactopyranosyl)‐__β__‐D‐mannopyranose (**10**) and the corresponding __α__‐D‐glucopyranose‐type glycosyl do
The glycosylation of pyrimidine bases with 2-deoxy-3,5-di-O-(p-toluoy1)-a-D-erythro-pentofuranosyl chloride (7) yields mixtures of This confirmed earlier observations that O/N transformation is not stereospecific in that caseI4'. However, the reac-
## Abstract For Abstract see ChemInform Abstract in Full Text.