"UMPOLUNG" OF REACTIVITY AT THE C-6 POSITION OF URIDINE: A SIMPLE AND GENERAL METHOD FOR 6-SUBSTITUTED URIDINES

DOI: 10.1016/0040-4020(82)80016-1

Source and publish data:

Tetrahedron p. 2635 - 2642 (1982)

Update date:2022-08-03

Topics:

Authors:

Tanaka, Hiromichi

Hayakawa, Hiroyuki

Miyasaka, Tadashi

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

Article abstract of DOI:10.1016/0040-4020(82)80016-1

Lithiated 2',3'-O-isopropylidene-5'-O-methoxymethyl-uridine was found to react with a variety of electrophilic reagents regiospecifically at the C-6 position.The protecting groups of the ribose moiety in the 6-functionalized products were concurrently rem

Full text of DOI:10.1016/0040-4020(82)80016-1

Products guided by the article

Product name:6-(1-hydroxycyclohexyl)-2',3'-O-isopropylidene-5'-O-methoxymethyluridine

Cas No:80614-88-6

R&D Labs maybe for 80614-88-6

HuiFeiChem PharmaTech Co.Ltd

Contact:0510-85393305

Address:1619 Huishan Avenue, Huishan District, Wuxi,
Dalian Synco Chemical Co., Ltd.

Contact:+86-411-83635150

Address:Rm 1004, 24, Tangshan Street, Dalian
Jiangxi Lanqi Fine Chemical S&T Co., Ltd.

Contact:+86-21-64891143

Address:XinJiShan Industrial Area, Zhangshu City, JiangXi Province, China
Hotechem Shanghai Co., Ltd

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

Address:Suite 2,No.2715 Longwu Road
Weifang Dongxing Chitosan Factory

website:http://dxchitosan.lookchem.com/

Contact:13475651157

Address:Weifang city ,shandong province

Relevant to this article

Synthesis of 2′,3′-dideoxy-6′,6′- difluorocarbocyclic nucleosides

Doi:10.1021/ol0482947
(2004)
Doi:10.1002/hlca.19520350526
(1952)
Fluorine-Containing Amino Acids and Their Derivatives. 3. Stereoselective Synthesis and Unusual Conformational Features of threo- and erythro-3-Fluorophenylalanine

Doi:10.1021/jo00181a003
(1984)
Doi:10.1093/gerona/56.12.B510
(1936)
On the Palladium-Catalyzed Alkylation of Silyl-Substituted Allyl Acetates with Enolates

Doi:10.1021/jo00177a016
(1984)
Synthesis of carbamates and ureas using Zr(IV)-catalyzed exchange processes

Doi:10.1021/ol0702728
(2007)

Article Doi