818. The chemical synthesis of polysaccharides. Part III. Positions of alkylation in a partly methylated amylose

B. J. Bines; W. J. Whelan

doi:10.1039/jr9620004232

818. The chemical synthesis of polysaccharides. Part III. Positions of alkylation in a partly methylated amylose

B. J. Bines, W. J. Whelan

Biochemistry & Molecular Biology

Research output: Contribution to journal › Article

1 Scopus citations

Abstract

A "mono-O-methylamylose," prepared by a method claimed to secure selective methylation of the 2-hydroxyl group, is proved to be rather randomly methylated, with only a limited excess of methyl at C-2. A new derivative of 2-O-methyl-D-glucose is reported.

Original language	English (US)
Pages (from-to)	4232-4233
Number of pages	2
Journal	Journal of the Chemical Society (Resumed)
DOIs	https://doi.org/10.1039/jr9620004232
State	Published - 1962

ASJC Scopus subject areas

Chemistry(all)

Access to Document

10.1039/jr9620004232

Fingerprint Dive into the research topics of '818. The chemical synthesis of polysaccharides. Part III. Positions of alkylation in a partly methylated amylose'. Together they form a unique fingerprint.

Cite this

@article{fc9be36e2f354e559d085b0da60c0bf9,

title = "818. The chemical synthesis of polysaccharides. Part III. Positions of alkylation in a partly methylated amylose",

abstract = "A {"}mono-O-methylamylose,{"} prepared by a method claimed to secure selective methylation of the 2-hydroxyl group, is proved to be rather randomly methylated, with only a limited excess of methyl at C-2. A new derivative of 2-O-methyl-D-glucose is reported.",

author = "Bines, {B. J.} and Whelan, {W. J.}",

year = "1962",

doi = "10.1039/jr9620004232",

language = "English (US)",

pages = "4232--4233",

journal = "Journal of the Chemical Society",

issn = "0577-6171",

publisher = "Chemical Society",

}

TY - JOUR

T1 - 818. The chemical synthesis of polysaccharides. Part III. Positions of alkylation in a partly methylated amylose

AU - Bines, B. J.

AU - Whelan, W. J.

PY - 1962

Y1 - 1962

N2 - A "mono-O-methylamylose," prepared by a method claimed to secure selective methylation of the 2-hydroxyl group, is proved to be rather randomly methylated, with only a limited excess of methyl at C-2. A new derivative of 2-O-methyl-D-glucose is reported.

AB - A "mono-O-methylamylose," prepared by a method claimed to secure selective methylation of the 2-hydroxyl group, is proved to be rather randomly methylated, with only a limited excess of methyl at C-2. A new derivative of 2-O-methyl-D-glucose is reported.

UR - http://www.scopus.com/inward/record.url?scp=37049063808&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=37049063808&partnerID=8YFLogxK

U2 - 10.1039/jr9620004232

DO - 10.1039/jr9620004232

M3 - Article

AN - SCOPUS:37049063808

SP - 4232

EP - 4233

JO - Journal of the Chemical Society

JF - Journal of the Chemical Society

SN - 0577-6171

ER -