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Syntheses with partially benzylated sugars. XI. Studies on the synthesis of the anomeric 5,6-dimethyl-1-D-ribofuranosylbenzimidazoles (ribazoles). Comparison of the condensation of 2,3,5-tri-O)-benzoyl-D-ribofuranosyl bromide and 2,3,5-tri-O-benzyl-D-ribofuranosyl chloride with 5,6-dimethylbenzimidazole.

作者信息

Stevens J D, Ness R K, Fletcher H G

出版信息

J Org Chem. 1968 May;33(5):1806-10. doi: 10.1021/jo01269a022.

DOI:10.1021/jo01269a022
PMID:5655928
Abstract
摘要

相似文献

1
Syntheses with partially benzylated sugars. XI. Studies on the synthesis of the anomeric 5,6-dimethyl-1-D-ribofuranosylbenzimidazoles (ribazoles). Comparison of the condensation of 2,3,5-tri-O)-benzoyl-D-ribofuranosyl bromide and 2,3,5-tri-O-benzyl-D-ribofuranosyl chloride with 5,6-dimethylbenzimidazole.部分苄基化糖的合成。十一。异头5,6-二甲基-1-D-呋喃核糖基苯并咪唑(利巴唑)合成的研究。2,3,5-三-O-苯甲酰基-D-呋喃核糖基溴和2,3,5-三-O-苄基-D-呋喃核糖基氯与5,6-二甲基苯并咪唑缩合反应的比较。
J Org Chem. 1968 May;33(5):1806-10. doi: 10.1021/jo01269a022.
2
Syntheses with partially benzylated sugars. XII. 3,5,-Di-O-benzyl-beta-D-ribofuranose and its use as an intermediate in the synthesis of partially substituted ribo nucleosides.部分苄基化糖的合成。十二。3,5-二-O-苄基-β-D-呋喃核糖及其作为合成部分取代核糖核苷中间体的用途。
J Org Chem. 1968 May;33(5):1810-5. doi: 10.1021/jo01269a023.
3
2,3,5-Tri-O-benzoyl-1-O-(p-nitrobenzoyl)- -D-ribofuranose, a convenient reagent for the preparation of 2,3,5-tri-O-benzoyl-D-ribofuranosyl chloride and bromide.2,3,5-三-O-苯甲酰基-1-O-(对硝基苯甲酰基)-β-D-呋喃核糖,一种用于制备2,3,5-三-O-苯甲酰基-D-核糖基氯和溴的便捷试剂。
Carbohydr Res. 1971 Oct;19(3):423-9. doi: 10.1016/s0008-6215(00)86177-7.
4
The synthesis of D-ribofuranosyl derivatives of methyl propiolate and a study of the activating influence of the ester group in cycloaddition reactions.
Carbohydr Res. 1977 May;55:225-38. doi: 10.1016/s0008-6215(00)84457-2.
5
C-nucleoside studies. Part 6. Synthesis of 3-[2,3,5-tri-O-benzyl-beta-(and alpha)-D-ribofuranosyl]prop-2-yn-1-ol and related compounds; a new synthesis of 3(5)-(2,3,5-tri-O-benzyl-beta-D-ribofuranosyl)pyrazole.C-核苷研究。第6部分。3-[2,3,5-三-O-苄基-β-(和α)-D-呋喃核糖基]丙-2-炔-1-醇及相关化合物的合成;3(5)-(2,3,5-三-O-苄基-β-D-呋喃核糖基)吡唑的新合成方法。
J Chem Soc Perkin 1. 1977 Aug;15:1786-91.
6
Syntheses with partially benzylated surgars. 13. Unsatur0td derivatives from 2,3,4,6-tetra-O-benzyl-N,N-dimethyl-5-O-(methylsulfonyl)-D-gluconamide by a novel type of elimination reaction.部分苄基化糖类的合成。13. 通过新型消除反应由2,3,4,6-四-O-苄基-N,N-二甲基-5-O-(甲基磺酰基)-D-葡糖酰胺制备的不饱和衍生物。
J Org Chem. 1968 May;33(5):1816-9. doi: 10.1021/jo01269a024.
7
Chemical modification of aminocyclitol antibiotics.
Carbohydr Res. 1976 Dec;52:187-96. doi: 10.1016/s0008-6215(00)85959-5.
8
A new synthesis of certain 7-(beta-D-ribofuranosyl) and 7-(2-deoxy-beta-D-ribofuranosyl) derivatives of 3-deazaguanine via the sodium salt glycosylation procedure.通过钠盐糖基化方法对某些3-脱氮鸟嘌呤的7-(β-D-呋喃核糖基)和7-(2-脱氧-β-D-呋喃核糖基)衍生物进行新的合成。
Nucleic Acids Res. 1985 Jul 25;13(14):5341-52. doi: 10.1093/nar/13.14.5341.
9
C-nucleoside studies. I. Synthesis of (2,3,5-tri-O-benzyl-alpha(and beta)-D-ribofuranosyl)ethyne.C-核苷研究。I. (2,3,5-三-O-苄基-α(和β)-D-核糖呋喃糖基)乙炔的合成。
J Chem Soc Perkin 1. 1974;0(16):1943-9.
10
Synthesis of Poly(ADP-ribose) Monomer Containing 2'-O-α-D-Ribofuranosyl Adenosine.含2'-O-α-D-呋喃核糖基腺苷的聚(ADP-核糖)单体的合成
Curr Protoc Nucleic Acid Chem. 2019 Sep;78(1):e92. doi: 10.1002/cpnc.92.

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Vitamin B(12) and alpha-Ribonucleosides.维生素B12与α-核糖核苷
Tetrahedron. 2008 Jan 1;64(1):9-38. doi: 10.1016/j.tet.2007.08.061.
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Regioselective glycosylation: synthesis of alpha-indoline nucleosides.区域选择性糖基化:α-吲哚啉核苷的合成
Nucleosides Nucleotides Nucleic Acids. 2005;24(8):1147-65. doi: 10.1081/NCN-200067398.
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Total synthesis of certain 2-, 6-mono- and 2,6-disubstituted-tubercidin derivatives. Synthesis of tubercidin via the sodium salt glycosylation procedure.某些2-、6-单取代和2,6-二取代杀结核菌素衍生物的全合成。通过钠盐糖基化方法合成杀结核菌素。
Nucleic Acids Res. 1984 Jan 25;12(2):1179-92. doi: 10.1093/nar/12.2.1179.
4
A new synthesis of certain 7-(beta-D-ribofuranosyl) and 7-(2-deoxy-beta-D-ribofuranosyl) derivatives of 3-deazaguanine via the sodium salt glycosylation procedure.通过钠盐糖基化方法对某些3-脱氮鸟嘌呤的7-(β-D-呋喃核糖基)和7-(2-脱氧-β-D-呋喃核糖基)衍生物进行新的合成。
Nucleic Acids Res. 1985 Jul 25;13(14):5341-52. doi: 10.1093/nar/13.14.5341.