Scholarly article on 4-hydroxy-3-iodo-quinoline-2-carboxylic acid ethyl ester 855633-99-7 from Journal of the American Chemical Society p. 2570,2573

DOI: 10.1021/ja01216a044

Source and publish data:

Journal of the American Chemical Society p. 2570,2573 (1946)

Update date:2022-08-04

Topics:

Authors:

Surrey Surrey

Cutler Cutler

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

Article abstract of DOI:10.1021/ja01216a044

Full text of DOI:10.1021/ja01216a044

Products guided by the article

Product name:4-hydroxy-3-iodo-quinoline-2-carboxylic acid ethyl ester

Cas No:855633-99-7

R&D Labs maybe for 855633-99-7

Lyan Limited

Contact:86-021-52418058

Address:8/F, Building 6, Guiping Road No.333, Shanghai, 200233, China
Shanghai shibo Chemical Co., Ltd

Contact:+86-021-60753516

Address:688 Qiushi Road, Jinshan High-tech Park, Shanghai, China,201512
wuxi huabin bio-tech Co.,Ltd(expird)

Contact:86-0510-85133006

Address:hubin road NO157
Xi'an yuanfar international trade company

website:https://www.yuanfarchemical.com

Contact:86-029-88745613 ext 828

Address:Floor19th ,B Building, Oak Block,No.36 South Fenghui Road, Dev. Zone of High-Tech Ind.,Xi’an, China
Sarchem Laboratories, Inc.

Contact:732.938.2777

Address:5012 Industrial Road Farmingdale, NJ 07727

Relevant to this article

Doi:10.1139/v63-202
(1963)
Palladium(II)-catalyzed oxidative Heck coupling of thiazole-4-carboxylates

Doi:10.1016/j.tetlet.2011.08.088
(2011)
SYNTHESIS OF NUCLEOSIDE SULFONATES AND SULFONES

Doi:10.1016/S0040-4039(00)79642-0
(1991)
Synthesis and pharmacological evaluations of novel 2H-benzo[b][1,4]oxazin- 3(4H)-one derivatives as a new class of anti-cancer agents

Doi:10.1016/j.ejmech.2011.07.045
(2011)
Two-step conversion of carboxylic esters into distally fluorinated ketones: Via ring cleavage of cyclopropanol intermediates: Application of sulfinate salts as fluoroalkylating reagents

Doi:10.1039/c7ob00680b
(2017)
Design, synthesis, and polymerase-catalyzed incorporation of click-modified boronic acid-TTP analogues

Doi:10.1002/asia.201100229
(2011)

Article Doi

DOI: 10.1021/ja01216a044

Source and publish data: