Exclusive and complete introduction of amino groups and their N-sulfo and N-carboxymethyl groups into the 6-position of cellulose without the use of protecting groups
Authors:
- Hanno BaumannHBHanno Baumann
- 1 August 2002
- journal article
- Published by Elsevier in Carbohydrate Research
- Vol. 337 (14) , 1297-1307
Abstract
No abstract availableKeywords
This publication has 34 references indexed in Scilit:
- Concepts for preparation of novel regioselective modified cellulose derivatives sulfated, aminated, carboxylated and acetylated for hemocompatible ultrathin coatings on biomaterialsMacromolecular Chemistry and Physics, 2000
- Effect of Substituents on Dielectric β-Relaxation in CellulosePolymer International, 1997
- Cationic Ring-Opening Polymerization of 3,6-Di-O-benzyl-α-d-glucose 1,2,4-Orthopivalate and the First Chemical Synthesis of CelluloseJournal of the American Chemical Society, 1996
- Facile synthesis of chiral glycine from D-riboseThe Journal of Organic Chemistry, 1985
- Synthesis of cis- and trans-1,3,5,7-tetranitro-1,3,5,7-tetraazadecalinThe Journal of Organic Chemistry, 1984
- SYNTHESIS OF 6-AMINO-6-DEOXYCELLULOSESen'i Gakkaishi, 1979
- Reduction of Organic Azides to Primary Amines with Lithium Aluminum HydrideJournal of the American Chemical Society, 1951
- The Rate of Esterification of Primary and Secondary Hydroxyls of Cellulose with p-Toluenesulfonyl (Tosyl) Chloride1Journal of the American Chemical Society, 1950
- The Unesterified Primary Hydroxyls in Acetone Soluble Cellulose AcetateJournal of the American Chemical Society, 1939
- A METHOD FOR THE IDENTIFICATION AND ESTIMATION OF THE 6-HYDROXYL GROUP IN GLUCOSEJournal of the American Chemical Society, 1932