STUDY ON CATIONIC RING-OPENING COPOLYMERIZATION OF 1,4-ANHYDRO-2,3-DI-O-BENZYL-α-D-RIBOPYRANOSE WITH 1,4-ANHYDRO-2,3-O-ISOPROPYLIDENE-α-D-RIBOPYRANOSE
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STUDY ON CATIONIC RING-OPENING COPOLYMERIZATION OF 1,4-ANHYDRO-2,3-DI-O-BENZYL-α-D-RIBOPYRANOSE WITH 1,4-ANHYDRO-2,3-O-ISOPROPYLIDENE-α-D-RIBOPYRANOSE
STUDY ON CATIONIC RING-OPENING COPOLYMERIZATION OF 1,4-ANHYDRO-2,3-DI-O-BENZYL-α-D-RIBOPYRANOSE WITH 1,4-ANHYDRO-2,3-O-ISOPROPYLIDENE-α-D-RIBOPYRANOSE
高分子科学(英文版)1997年15卷第3期 页码:282-288
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纸质出版:1997-09-20
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WU Chengpei, PAN Caiyuan, Toshiyuki Uryu. STUDY ON CATIONIC RING-OPENING COPOLYMERIZATION OF 1,4-ANHYDRO-2,3-DI-O-BENZYL-α-D-RIBOPYRANOSE WITH 1,4-ANHYDRO-2,3-O-ISOPROPYLIDENE-α-D-RIBOPYRANOSE[J]. 高分子科学(英文版), 1997,15(3):282-288.
WU Chengpei, PAN Caiyuan, Toshiyuki Uryu. STUDY ON CATIONIC RING-OPENING COPOLYMERIZATION OF 1,4-ANHYDRO-2,3-DI-O-BENZYL-α-D-RIBOPYRANOSE WITH 1,4-ANHYDRO-2,3-O-ISOPROPYLIDENE-α-D-RIBOPYRANOSE[J]. 1997, 15(3): 282-288.
WU Chengpei, PAN Caiyuan, Toshiyuki Uryu. STUDY ON CATIONIC RING-OPENING COPOLYMERIZATION OF 1,4-ANHYDRO-2,3-DI-O-BENZYL-α-D-RIBOPYRANOSE WITH 1,4-ANHYDRO-2,3-O-ISOPROPYLIDENE-α-D-RIBOPYRANOSE[J]. 高分子科学(英文版), 1997,15(3):282-288.DOI:
WU Chengpei, PAN Caiyuan, Toshiyuki Uryu. STUDY ON CATIONIC RING-OPENING COPOLYMERIZATION OF 1,4-ANHYDRO-2,3-DI-O-BENZYL-α-D-RIBOPYRANOSE WITH 1,4-ANHYDRO-2,3-O-ISOPROPYLIDENE-α-D-RIBOPYRANOSE[J]. 1997, 15(3): 282-288.DOI:
STUDY ON CATIONIC RING-OPENING COPOLYMERIZATION OF 1,4-ANHYDRO-2,3-DI-O-BENZYL-α-D-RIBOPYRANOSE WITH 1,4-ANHYDRO-2,3-O-ISOPROPYLIDENE-α-D-RIBOPYRANOSE
3-O-isopropylidene-α-D-ribo-pyranose (AIRP) with 1
4-anhydro-2
3-di-O-benzyl-α-D-ribopyranose (ADBR) preparedfrom D-ribose was studied. Copolymerization using SbCl5 or BF3 OEt2 as catalyst atlow temperature gave stereoregular (1→4)β-D-ribofuranan (C-1 and C-4 ring cleavagesee Scheme 1) or (1→5) α-D-ribofuranan (C-1 and C-5 ring cleavage) respectively. Theeffects of catalysts
reaction time and temperatures on yield and stereoregularity of the ob-tained polymers were studied.Polymers were charaterized by molecular weight
1H NMR
13C NMR and optical rotation.
Abstract
Cationic ring-opening copolymerization of 1
4-anhydro-2
3-O-isopropylidene-α-D-ribo-pyranose (AIRP) with 1
4-anhydro-2
3-di-O-benzyl-α-D-ribopyranose (ADBR) preparedfrom D-ribose was studied. Copolymerization using SbCl5 or BF3 OEt2 as catalyst atlow temperature gave stereoregular (1→4)β-D-ribofuranan (C-1 and C-4 ring cleavagesee Scheme 1) or (1→5) α-D-ribofuranan (C-1 and C-5 ring cleavage) respectively. Theeffects of catalysts
reaction time and temperatures on yield and stereoregularity of the ob-tained polymers were studied.Polymers were charaterized by molecular weight
1H NMR
13C NMR and optical rotation.
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