Scholarly article on 1,6-Anhydro-β-D-gulopyranose tribenzoate 33297-50-6 from Journal of the American Chemical Society p. 1021,1023

DOI: 10.1021/ja01609a067

Source and publish data:

Journal of the American Chemical Society p. 1021,1023 (1955)

Update date:2022-08-03

Topics:

Authors:

Stewart Stewart

Richtmyer

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

Article abstract of DOI:10.1021/ja01609a067

Full text of DOI:10.1021/ja01609a067

Products guided by the article

Product name:1,6-Anhydro-β-D-gulopyranose tribenzoate

Cas No:33297-50-6

R&D Labs maybe for 33297-50-6

Shanghai Cheerchem Co., Ltd.

Contact:86-21-50966856

Address:Building 5,300 Chuanzhan Road,Pudong New District,Shanghai
Shaanxi HuaTai Bio-fine chemical company Ltd

Contact:86-029-87862197

Address:No. 5, 3rd Floor, 29 Yanta North Road, Beilin Dist.
Xinjiang Zhongtai Chemical Co., Ltd.

Contact:+86-991-8788172

Address:NO.78 XISHAN RD.URUMQI，CHINA
Taizhou Chemedir Biopharm-tech Co., Ltd

Contact:+86 523 86200218

Address:G09, No. 1 Avenue China Medical City, Taizhou,Jiangsu, China
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

Relevant to this article

Pyridoindole derivative as electron transporting host material for efficient deep-blue phosphorescent organic light-emitting diodes

Doi:10.1002/adma.201001221
(2010)
Reaction of rhenium alkynyl carbene complexes with tertiary phosphines produces dihydrophospholium rhenium complexes by a formal CH insertion process

Doi:10.1016/S0022-328X(00)00733-6
(2001)
Syntheses of palladated aryldithioacetals. Unexpected rearrangement involving C-S and C-Pd bonds

Doi:10.1021/om0008981
(2001)
Synthesis and biological evaluation of salicylic acid conjugated isoxazoline analogues on immune cell proliferation and angiogenesis

Doi:10.1016/j.ejmech.2016.02.052
(2016)
Synthesis of enantiomerically enriched β,γ-unsaturated-α-amino acids

Doi:10.1016/S0040-4020(00)01146-7
(2001)
Revisit to the reduction of allylic chlorides to less substituted olefins by a low-valent chromium species in the presence of a proton source

Doi:10.1016/S0040-4039(00)02140-7
(2001)

Article Doi

DOI: 10.1021/ja01609a067