Synthesis of dextran derivatives by ring‐opening polymerization, 1. Synthetic dextran derivatives having partially primary hydroxyl groups

Ikeda, Yuko; Yonezawa, Takaki; Kimura, Hiroyuki; Kohjiya, Shinzo; Okada, Masahiko

doi:10.1002/marc.1993.030140904

Cited by 1 publication

(2 citation statements)

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“…[95] Copolymerization of monomers with different substituents (Bn, C 2 H 5 OBn) gave polymers that could be reduced via the Birch reduction to produce dextran derivatives with primary hydroxyl groups. The stereocontrol of the anomeric carbon atom was perfectly a-isomeric.…”

Section: Synthesismentioning

confidence: 99%

“…Dextran derivatives having partially primary hydroxyl groups were synthesized by ring‐opening polymerization of bicyclic acetals (Scheme ) 95. Copolymerization of monomers with different substituents (Bn, C 2 H 5 OBn) gave polymers that could be reduced via the Birch reduction to produce dextran derivatives with primary hydroxyl groups.…”

Section: Polysaccharidesmentioning

confidence: 99%

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Biomacromolecules and Bio‐Related Macromolecules

Kobayashi

Uyama

2003

Macro Chemistry & Physics

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The present article briefly reviews research developments in the area of biomacromolecules and bio‐related macromolecules, whose research papers have been published for several decades preferably in the Macromolecular Journals. The area covers the important classes of macromolecules, polysaccharides (cellulose, amylose, chitin, etc.), polyesters (poly(lactic acid), poly(hydroxyalkanoate)s, etc.), and phenolic polymers (lignin, urushi, etc.). These polymers and their derivatives are very important for scientific interests as well as for industrial applications. Their synthesis, structure, reactions, and properties are mainly mentioned, and important topics of the target polymers are selected and mostly chronologically reviewed.

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Section: Synthesismentioning

confidence: 99%

Section: Polysaccharidesmentioning

confidence: 99%