4-Aidobutyryl Group for Temporary Protection of Hydroxyl Functions

DOI: 10.1246/bcsj.59.1296

Source and publish data:

Bulletin of the Chemical Society of Japan p. 1296 - 1298 (1986)

Update date:2022-08-03

Topics:

Authors:

Kusumoto, Shoichi

Sakai, Keiichiro

Shiba, Tetsuo

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

Article abstract of DOI:10.1246/bcsj.59.1296

4-Azidobutyryl esters formed from hydroxyl compounds and 4-azidobutyryl chloride were shown to be cleaved via reduction to 4-aminobutyrate followed by intramolecular O->N-acyl migrations to regenerate the free hydroxyl groups.High susceptibility of aide g

Full text of DOI:10.1246/bcsj.59.1296

Products guided by the article

Product name:allyl 2-acetamido-4-O-(4-azidobutyryl)-3,6-di-O-benzoyl-2-deoxy-β-D-glucopyranoside

Cas No:102689-59-8

R&D Labs maybe for 102689-59-8

Hunan Haili Chemical Industry Co.,Ltd.

Contact:+86-731-85521860

Address:No.251, 2nd Section, Furong Road, Changsha,Hunan,China
Nanjing distinctions Medical Technology Co., Ltd.(expird)

Contact:+86-15996203785 13914714059

Address:nanjing,jiangsu , China
Antaeus Bio-technology Co., LTD(expird)

Contact:021-31252569

Address:shanghai pudong
Xiamen Huasing Chemicals Co.Ltd.

Contact:0086-592-6228397

Address:NO.24, Xinglin North 2nd Road,Jimei district
Guangzhou Shiny Co., Ltd.

website:https://www.sinoshiny.com/products

Contact:+86-20-62802632;62802633

Address:Room 330 GIGCAS Building,No.511 Kehua Street,Tianhe District

Relevant to this article

Ruthenium-catalyzed 1,3-dipolar cycloaddition of trifluoromethylated propargylic alcohols with azides

Doi:10.1016/j.tetlet.2008.04.065
(2008)
Stereospecific synthesis of functionalized C5-unsaturated hydantoin derivatives via a three-component reaction

Doi:10.1055/s-2008-1066993
(2008)
An efficient glycosylation protocol with glycosyl ortho-alkynylbenzoates as donors under the catalysis of Ph₃PAuOTf

Doi:10.1016/j.tetlet.2008.04.017
(2008)
Studies related to cephalosporins. Part 2 [1a]. Displacement reactions on 3-bromomethylcephems with salts of carboxylic acids

Doi:10.1002/jhet.5570220414
(1985)
Design, synthesis, and pharmacological evaluation of 2-(4-sulfonylphenyl)-2-[(E)-pyrrolidin-1-ylimino]-N-thiazoleacetamides as glucokinase activators

Doi:10.1016/j.bmcl.2020.127249
(2020)
Comparative pharmacology in the rat of ketamine and its two principal metabolites, norketamine and (Z)-6-hydroxynorketamine

Doi:10.1021/jm00161a043
(1986)

Article Doi