N.m.r. spectroscopic studies (iH, 13C) have shown that hydroxylamine and hydrazine react with 2,3-O-isopropylidene-D-ribofuranose (1) and D-ribose (2) to give primarily the acyclic oxime and hydrazone, respectively, whereas thiosemicarbazide affords mainly the cyclic pyranosyl and furanosyl derivat
✦ LIBER ✦
N.m.r. studies of d-ribosylamines in solution: Derivatives of primary amines
✍ Scribed by Claude Chavis; Chantal de Gourcy; Françoise Dumont; Jean-Louis Imbach
- Book ID
- 107725319
- Publisher
- Elsevier Science
- Year
- 1983
- Tongue
- English
- Weight
- 983 KB
- Volume
- 113
- Category
- Article
- ISSN
- 0008-6215
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
N.m.r. studies of d-ribosylamines in sol
✍
Claude Chavis; Chantal De Gourcy; Jean-Louis Imbach
📂
Article
📅
1984
🏛
Elsevier Science
🌐
English
⚖ 790 KB
N.m.r. and c.d. studies of the DNA fragm
✍
Vladimir Sklenář; Jaroslav Kypr; Ad Bax; Gerald Zon; Michaela Vorličkova
📂
Article
📅
1989
🏛
Elsevier Science
🌐
English
⚖ 411 KB
N.m.r. Studies of Pyrimidine, Imidazole
✍
Reddy, G. S.; Hobgood, R. T.; Goldstein, J. H.
📂
Article
📅
1962
🏛
American Chemical Society
🌐
English
⚖ 557 KB
Proton-n.m.r. studies of some N-acetylgl
✍
Alberto B. Zanlungo; Alberto S. Cerezo
📂
Article
📅
1981
🏛
Elsevier Science
🌐
English
⚖ 203 KB
Crystalline furanose derivatives of 3-de
✍
Cecile du Mortier; Rosa M. de Lederkremer
📂
Article
📅
1985
🏛
Elsevier Science
🌐
English
⚖ 539 KB
Debenzoylation of 2,4,6-tri-O-benzoyl-3-deoxy-D-arabino-hexono-l,S-lactone (1) followed by heating in vacua and rebenzoylation afforded 2,5,6-tri-o-benzoyl-3-deoxy-D-arubino-hexono-1,Clactone (2). Reduction of 2 with disiamylborane gave 2,5,6-tri-O-benzoyl-3-deoxy-D-arabino-hexofuranose (3) a conven
Near-infrared N-H bands of primary aroma
✍
Kermit B. Whetsel
📂
Article
📅
1961
🏛
Elsevier Science
⚖ 990 KB