Scholarly article on 1,2,3,4-TETRA-O-ACETYL-ALPHA-D-ARABINOPYRANOSE 108646-05-5 from Journal of the American Chemical Society p. 3012,3014

DOI: 10.1021/ja01266a008

Source and publish data:

Journal of the American Chemical Society p. 3012,3014 (1939)

Update date:2022-08-17

Topics:

Authors:

Klingensmith

Evans Evans

Read Full Text PDF DownLoad Join now for total 90,000,000 free articles

Article abstract of DOI:10.1021/ja01266a008

Full text of DOI:10.1021/ja01266a008

Products guided by the article

Product name:1,2,3,4-TETRA-O-ACETYL-ALPHA-D-ARABINOPYRANOSE

Cas No:108646-05-5

R&D Labs maybe for 108646-05-5

GUANGZHOU MEDCAN PHARMATECH LTD

website:http://www.gzmedcan.com

Contact:+86-20-82519649

Address:Building J,Room 101,1 JiangtashanRd,Guang Zhou Science City,Guang Zhou ,China
ZiBO KuoDing Trade company Ltd

website:http://www.sdzbkd.com

Contact:86-13361591822

Address:GongQingTuan road
Nantong Auxin Electronic Technology Co., LTD

Contact:86-513-88760026

Address:NO.5-1, Aoxin Road, Haian Hi-tech Development Zone, Jiangsu Province, China
Aqua Chem Industry Co., Ltd

Contact:+86-515-88356562

Address:No.2, West Daqing Road, Yancheng, Jiangsu, China
Zhejiang Golden-Shell Pharmaceutical Co.,Ltd.

Contact:+86-576-87501888 / 87501988

Address:No.89 Zhongxing Road. Li'ao, Yuhuan, Zhejiang, China

Relevant to this article

A long-range emissive mega-Stokes inorganic-organic hybrid material with peripheral carboxyl functionality for As(v) recognition and its application in bioimaging

Doi:10.1039/c7dt02387a
(2017)
Facile Preparation of Nitrones by Electrochemical Oxidation of N-Hydroxy Secondary Amines Using Halogen Ions as Mediators

Doi:10.1021/jo00354a031
(1986)
Catalysis by methyltrioxorhenium(VII): Reduction of hydronium ions by europium(II) and reduction of perchlorate ions by europium(II) and chromium(II)

Doi:10.1021/ic048669k
(2005)
RhNPs supported onN-functionalized mesoporous silica: effect on catalyst stabilization and catalytic activity

Doi:10.1039/d0dt04213g
(2021)
Efficient catalytic racemization of secondary alcohols

Doi:10.1016/S0040-4039(98)01116-2
(1998)
Doi:10.1016/0039-128X(63)90014-X
(1963)

Article Doi

DOI: 10.1021/ja01266a008