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

TIANJIN DONGRUXIANG MINERALS MARKETING CO.,LTD(expird)

Contact:22-58516360

Address:tianjin
shanghai hekang chemical co.ltd

Contact:021-54173790

Address:328 WuHe Road, Building #A, 2nd Floor, Minhang, Shanghai 201109, China
FOSHAN NANHAI ZHONGNAN PHARMACEUTICAL FACTORY

Contact:0086-0757-85609331

Address:XIAHENGTIAN INDUSTRIAL ZONE,SHAYONG VILLAGE,LISHUI TOWN
Tianjin Ji Ping Jia Chemical Co., Ltd.

Contact:18622448868

Address:tianjin
Shanghai Sunwise Chemical Co., Ltd

website:http://www.sunwisechem.com

Contact:86-021-33883180

Address:Room 10E, Building G, Westlink Center, No. 2337 Gudai Road, Minhang District, Shanghai, China PC: 201100

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