Cellulose Oligomers: Preparation from Cellulose Triacetate, Chemical Transformations and Reactions

被引:0
作者
P. Arndt
K. Bockholt
R. Gerdes
S. Huschens
J. Pyplo
H. Redlich
K. Samm
机构
[1] Westfälische Wilhelms-Universität Münster,Organisch
来源
Cellulose | 2003年 / 10卷
关键词
Acylysis; Pivaloylysis; Unidisperse and branched cellulose units;
D O I
暂无
中图分类号
学科分类号
摘要
Cellulose oligomers obtained by a new degradation method (pivaloylysis) are used as starting materials in organic synthesis. On the one hand these oligomers are functionalized to potent glycosyl donors, on the other hand several methods are shown to generate different types of hydroxy compounds (glycosyl acceptors). Glycosidation reactions performed with these two types of building blocks allow an access to linear products (unidisperse celluloses) as well as to new branched cellulose units.
引用
收藏
页码:75 / 83
页数:8
相关论文
共 50 条
[1]  
Arasappan A.(1996)n-Pentenyl glycoside methodology in the stereoselective construction of the tetrasaccharyl cap portion of J. Org. Chem. 61 2401-2406
[2]  
Fraser-Reid B.(1998) lipophosphoglycan Chem. Lett. 12 1273-1275
[3]  
Chandrasekhar S.(1988)Regioselective reductive ring opening of cyclic benzylidene acetals Indian J. Chem. Sect. B 27B 527-529
[4]  
Ravinda Reddy Y.(1995)A method for the selective reduction of carbohydrate 4,6- Tetrahedron Lett. 36 669-672
[5]  
Raji Reddy C.(1963)-benzylidene acetals Meth. Carbohydr. Chem. II 307-308
[6]  
Dasgupta F.(1879)Cyclic acetals derivatives: benzylidene acetals Ber. Dtsch. Chem. Ges. 12 1938-1942
[7]  
Singh P.(1982)Ñber Kohlehydrate Carbohydr. Res. 108 97-101
[8]  
Srivastava H.(1980)A novel reductive ringopening of carbohydrate benzylidene acetals Carbohydr. Res. 80 C17-C22
[9]  
DeNinno M.P.(1960)Chemistry of the glycosidic linkage: exceptionally fast and efficient formation of glycosides by remote activation Acta Chem. Scand. 14 877-881
[10]  
Etienne J.B.(1991)Action of strong acids on acetylated glycosides J. Am. Chem. Soc. 113 3079-3084