Total synthesis of C-glycoside fragment of nogalamycin

DOI: 10.1039/c39830000896

Source and publish data:

Journal of the Chemical Society. Chemical communications p. 896 - 898 (1983)

Update date:2022-08-05

Topics:

Authors:

Bates Bates

Sammes Sammes

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

Article abstract of DOI:10.1039/c39830000896

Full text of DOI:10.1039/c39830000896

View Article Online / Journal Homepage / Table of Contents for this issue

View Article Online

Products guided by the article

Product name:8-benzyloxy-9-bromo-2,6-epoxy-4-dimethylamino-3,5-dihydroxy-6-methyl-3,4,5,6-tetrahydro-2H-1-benzoxecane

Cas No:88278-19-7

R&D Labs maybe for 88278-19-7

Chengda Pharmaceuticals Co., Ltd.

Contact:+86-573-84601188

Address:hengshan Road 5# in Jiashan, zhejiang
Jiangsu Cale New Material Co.ltd

Contact:+86-515-88334667/88203550

Address:Zhongshan 3rd Road, Coastal Chemical Industry Park, Yancheng, Jiangsu, China
Binzhou Holly Pharmaceutical Co.,Ltd.

Contact:74517

Address:No.15 Dapu Road,Huangpu District Shanghai,P.R.China
Hotechem Shanghai Co., Ltd

Contact:13120882795；+86-21-34621078;+86-021-31122318

Address:Suite 2,No.2715 Longwu Road
zhangjiagang bonded areas banggao co;ltd

website:http://www.shunchangchem.com

Contact:0086-13921972933

Address:Dongsha Chemical Zone.Zhangjiagang, Jiangsu Province

Relevant to this article

Mixed-ligand copper complexes with 8-methylthioquinoline and triphenylphosphane or the o-semiquinone/catecholate redox system

Doi:10.1002/ejic.200500567
(2005)
Doi:10.1021/ja01170a027
(1949)
Synthesis of metal dithiolene complexes by Si-S bond cleavage of a bis(silanylsulfanyl)alkene

Doi:10.1016/j.ica.2005.09.067
(2006)
Anomalous face-selectivity in sharpless asymmetric dihydroxylation of o-allylbenzamides

Doi:10.1021/jo9607323
(1996)
An efficient synthesis of ferrocenyl substituted 3-cyanopyridine derivatives under ultrasound irradiation

Doi:10.1016/j.jorganchem.2005.09.046
(2006)
Synthesis of a phosphorylated disaccharide fragment of the O-specific polysaccharide of Vibrio cholerae O139, functionalized for conjugation

Doi:10.1002/hlca.200690036
(2006)

Article Doi