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

Shanghai doly chemical Co.,Ltd

Contact:+86-21-34716221

Address:No.328,WuHe Roard,MinHang,ShangHai China
Yancheng Smiling Imp & Exp Co., Ltd.

Contact:+86-515-83173586

Address:Rm1207, BLD#03, Phoenix Plaza, Juheng Road, Yancheng, Jiangsu, P.R. China
Hangzhou Ocean Chemical Co., Ltd.

website:http://www.hzoceanchem.com

Contact:+86-571-88025872, 28272092, 28272096

Address:Room 623 ,Building No 1 , COFCO Radius Commercial Center Xiwen Road, Xiacheng District, Hangzhou, Zhejiang Province, China
HANGZHOU ZHONGCHANG SCIENTIFIC CO.,LTD

Contact:+86-571-88932183

Address:Hangzhou
Nanjing Fred Technology Co.,Ltd.

website:http://www.fredbio.com

Contact:+86-25-84696168

Address:Nanjing

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