The synthesis of purpurosamine B derivatives

DOI: 10.1246/bcsj.54.2825

Source and publish data:

Bulletin of the Chemical Society of Japan p. 2825 - 2826 (1981)

Update date:2022-08-03

Topics:

Authors:

Honda Honda

Suami Suami

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

Article abstract of DOI:10.1246/bcsj.54.2825

Full text of DOI:10.1246/bcsj.54.2825

Products guided by the article

Product name:Methanesulfonic acid 1-((2S,5R,6S)-5-acetylamino-6-methoxy-tetrahydro-pyran-2-yl)-2-benzyloxycarbonylamino-ethyl ester

Cas No:79952-88-8

R&D Labs maybe for 79952-88-8

Shenyang Xingzhenghe Chemical Co., Ltd.

Contact:024-23509232

Address:No. 33, Naner Road, Heping Dist.
NANCHANG QINZHI SCI&TEC.CO.,LTD(expird)

Contact:+86-13687004106

Address:Hero South Road,Hero Zone,Nanchang,Jiangxi,China
Taizhou Chemedir Biopharm-tech Co., Ltd

Contact:+86 523 86200218

Address:G09, No. 1 Avenue China Medical City, Taizhou,Jiangsu, China
ClickChem Technology Co., Limited

Contact:+86-0310-6519966/0531-52893837

Address:No.750 Shunhua Road, High-Tech Zone, Jinan city, Shandong China
Jiangsu Cale New Material Co.ltd

Contact:+86-515-88334667/88203550

Address:Zhongshan 3rd Road, Coastal Chemical Industry Park, Yancheng, Jiangsu, China

Relevant to this article

Design, synthesis, and antiviral activity of certain 3-substituted 2,5,6-trichloroindole nucleosides

Doi:10.1021/jm0400146
(2004)
An effective and safe enkephalin analog for antinociception

Doi:10.3390/pharmaceutics13070927
(2021)
Doi:10.1021/ja01630a038
(1954)
OXIDATION-REDUCTION MECHANISMS - INNER-SPHERE AND OUTER-SPHERE ELECTRON TRANSFER IN THE REDUCTION OF IRON(III), RUTHENIUM(III), AND OSMIUM(III) COMPLEXES BY ALKYL RADICALS. MECHANISMS -

Doi:10.1021/ja00369a030
(1982)
Thermochemistry for the Gas-Phase Ion-Molecule Clustering of CO2⁺CO2, SO2⁺CO2, N2O⁺N2O, O2⁺CO2, NO⁺CO2, O2⁺N2O, and NO⁺N2O: Description of a New Hybrid Drift Tube/Ion Scoure with Coaxial Electron Beam and Ion Exit Apertures

Doi:10.1021/j100321a037
(1988)
Adriamycin analogues. Preparation and biological evaluation of some N-perfluoroacyl analogues of daunorubicin, adriamycin, and N-(trifluoroacetyl)adriamycin 14-valerate and their 9,10-anhydro derivatives

Doi:10.1021/jm00344a019
(1982)

Article Doi