Regioselective Bromination of O-β-Glycosylated Aromatics

DOI: 10.1016/0040-4039(95)00050-M

Source and publish data:

Tetrahedron Letters p. 1705 - 1708 (1995)

Update date:2022-09-26

Topics: Isolation Regioisomers Reaction mixture Bromination Protecting group Regioselective NMR Analysis Aromatics

Authors:

Mabic, Stephane

Lepoittevin, Jean-Pierre

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

Article abstract of DOI:10.1016/0040-4039(95)00050-M

The quasi quantitative and regioselective bromination of O-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl)phenols is described.The orientating effect of the glycoside group is compared with those of other oxygenated groups and its usefulness illustrated with

Full text of DOI:10.1016/0040-4039(95)00050-M

Products guided by the article

Product name:Acetic acid (2S,3R,4S,5R,6R)-4,5-diacetoxy-6-acetoxymethyl-2-(5-bromo-2-methoxy-phenoxy)-tetrahydro-pyran-3-yl ester

Cas No:163852-97-9

R&D Labs maybe for 163852-97-9

Lyrin Industrial Corporation Limited

Contact:86-731-82571800

Address:Rm 2408,Asia Economy International Building,Shaoshan Road South,Yuhua District,Changsha,Hunan,China
Hongyi Import & Export CO.,LTD

Contact:86-13319649499

Address:Nanzheng Neighborhood Commitees, Chongwen Office, Yongding District
HUNAN CHEMAPI BIOLOGICAL TECHNOLOGY CO.,LTD.

Contact:+86-186-02659358

Address:1004, building 3, Wanke Jinsemaitianyuan, 498 Guitang Road, Yuhua District, Changsha City, Hunan Province, China
Beijing Top Science biological technology co., LTD

Contact:+86-13439059536

Address:15-1705 jre three mile, Beijing 100000,CHINA
Hefei TNJ chemical industry co.,ltd

website:https://www.tnjchem.com

Contact:+86-551-65418695

Address:B911 Xincheng Business Center, Qianshan Road, Hefei Anhui China

Relevant to this article

Utilization of Solid Acid SO₄²^?/TiO₂ as Catalyst to the Three-Component Mannich Reaction at Ambient Temperature

Doi:10.1002/jhet.2825
(2017)
Direct C-H trifluoromethylation of di- and trisubstituted alkenes by photoredox catalysis

Doi:10.3762/bjoc.10.108
(2014)
Visible light mediated intermolecular [3 + 2] annulation of cyclopropylanilines with alkynes

Doi:10.3762/bjoc.10.96
(2014)
An efficient method for the synthesis of aromatic C-nucleosides

Doi:10.1016/0040-4039(95)00145-3
(1995)
Synthesis of spirocyclic enones by rhodium-catalyzed dearomatizing oxidative annulation of 2-alkenylphenols with alkynes and enynes

Doi:10.1002/chem.201403454
(2014)
(Trifluoromethyl)thiolation of 2-alkynylbenzoates: An efficient route to 4-[(trifluoromethyl)thio]-1H-isochromen-1-ones

Doi:10.1002/ejoc.201402629
(2014)

Article Doi