Syntheses of 6-O-ethyl/methyl-celluloses via ring-opening copolymerization of 3-O-benzyl-6-O-ethyl/methyl-α-d-glucopyranose 1,2,4-orthopivalates and their structure-property relationships
Preparation and characterization of monolayer and multilayer Langmuir-Blodgett films of a series of 6-O-alkylcelluloses
DOI 10.1021/bm0500603
S Ifuku S Nakai H Kamitakahara T Takano Y Tsujii F Nakatsubo 2005 Preparation and characterization of monolayer and multilayer langmuir-blodgett films of a series of 6-O-alkylcelluloses Biomacromolecules 6 4 2067 2073 10.1021/bm0500603 1:CAS:528:DC%2BD2MXkslOmsrw%3D (Pubitemid 41052200)
Substituent effect on ring-opening polymerization of regioselectively acylated α-D-glucopyranose 1,2,4-orthopivalate derivatives
H Kamitakahara M Hori F Nakatsubo 1996 Substituent effect on ring-opening polymerization of regioselectively acylated α-d-glucopyranose 1, 2, 4-orthopivalate derivatives Macromolecules 29 19 6126 6131 10.1021/ma960488h 1:CAS:528:DyaK28XltVWms7g%3D (Pubitemid 126544814)
Block co-oligomers of tri-O-methylated and unmodified cello-oligosaccharides as model compounds for methylcellulose and its dissolution/gelation behavior
DOI 10.1007/s10570-005-9003-6
H Kamitakahara F Nakatsubo D Klemm 2006 Block co-oligomers of tri-O-methylated and unmodified cello-oligosaccharides as model compounds for methylcellulose and its dissolution/gelation behavior Cellulose 13 4 375 392 10.1007/s10570-005-9003-6 1:CAS:528:DC%2BD28Xot1ahurs%3D (Pubitemid 44236467)
New class of carbohydrate-based nonionic surfactants: Diblock co-oligomers of tri-O-methylated and unmodified cello-oligosaccharides
DOI 10.1007/s10570-007-9128-x
H Kamitakahara F Nakatsubo D Klemm 2007 New class of carbohydrate-based nonionic surfactants: diblock co-oligomers of tri-O-methylated and unmodified cello-oligosaccharides Cellulose 14 5 513 528 10.1007/s10570-007-9128-x 1:CAS:528:DC%2BD2sXps1Gqsrk%3D (Pubitemid 47343236)
H Kamitakahara A Koschella Y Mikawa F Nakatsubo T Heinze D Klemm 2008 Syntheses and comparison of 2, 6-di-O-methyl celluloses from natural and synthetic celluloses Macromol Biosci 8 7 690 700 10.1002/mabi.200700291 1:CAS:528:DC%2BD1cXovFWgsL0%3D
Syntheses of 2,6-O-alkyl celluloses: Influence of methyl and ethyl groups regioselectively introduced at O-2 and O-6 positions on their solubility
doi: 10.1007/s10570-009-9332-y
Kamitakahara H, Funakoshi T, Takano T, Nakatsubo F (2009) Syntheses of 2,6-O-alkyl celluloses: influence of methyl and ethyl groups regioselectively introduced at O-2 and O-6 positions on their solubility. Cellulose. doi: 10.1007/s10570-009-9332-y
Karakawa M (2003) Chemical synthesis of high-regioselectively methylated celluloses by a cationic ring-opening polymerization (Kyoto). Ph.D. Thesis, Kyoto University
Cationic ring-opening polymerization of 3,6-di-O-benzyl-α-D-glucose 1,2,4-orthopivalate and the first chemical synthesis of cellulose
DOI 10.1021/ja953286u
F Nakatsubo H Kamitakahara M Hori 1996 Cationic ring-opening polymerization of 3, 6-di-O-benzyl-α-d-glucose 1, 2, 4-orthopivalate and the first chemical synthesis of cellulose J Am Chem Soc 118 7 1677 1681 10.1021/ja953286u 1:CAS:528:DyaK28XnvFCjug%3D%3D (Pubitemid 26092309)