Scholarly article on 2-(2-hydroxyimino-propionyl)-benzoic acid methyl ester 118836-67-2 from Journal of the American Chemical Society p. 542,544

DOI: 10.1021/ja01182a033

Source and publish data:

Journal of the American Chemical Society p. 542,544 (1948)

Update date:2022-07-31

Topics:

Authors:

Ullyot Ullyot

Taylor Taylor

Dawson Dawson

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

Article abstract of DOI:10.1021/ja01182a033

Full text of DOI:10.1021/ja01182a033

Products guided by the article

Product name:2-(2-hydroxyimino-propionyl)-benzoic acid methyl ester

Cas No:118836-67-2

R&D Labs maybe for 118836-67-2

Huludao Tianqi Shengye Chemical Co.,Ltd.

Contact:0086 429 2075777

Address:Area B,Shipbuilding Industry Park,Beigang District,Huludao City,Liaoning prov.,China
Jiangsu Chiatai Qingjiang Pharmaceutical Co.,Ltd

Contact:+86-517-86283327

Address:9 North Hantai Road, Huaian, China
NOVASYNCS CO., LTD

Contact:0512-63006287

Address:no.88.YISHENG Road,etdz-WUJIANG,SUZHOU,CHINA
Nanjing Qirui Material Co., Ltd.

Contact:+86-25-52320053

Address:F4-5, #17 Building, Chuang Yi Yuan, No.6 Guanghua East Street, Nanjing, 210007 P.R.China
JinTan Pingsheng Chemical Co.,Ltd

Contact:+86-519-82828200

Address:NO.11Danfengxilu Road,Jintan City,Jiangsu,China

Relevant to this article

1-Alkyl-2,3-dihydro-4(1H)-quinolinones by a tandem Michael-S_NAr annulation reaction

Doi:10.1002/jhet.70
(2009)
Nucleosides and nucleotides. 96. Synthesis and antitumor activity of 5-ethynyl-1-β-D-ribofuranosylimidazole-4-carboxamide (EICAR) and its derivatives

Doi:10.1021/jm00106a045
(1991)
Iron-catalyzed carbonylation: Selective and efficient synthesis of succinimides

Doi:10.1002/anie.200902078
()
Highly regio- and enantioselective copper-catalyzed hydroboration of styrenes

Doi:10.1002/anie.200902015
(2009)
Reagent-controlled enantioselectivity switch for the asymmetric fluorination of β-ketocarbonyls by chiral primary amine catalysis

Doi:10.1039/c6sc03109a
(2016)
Synthesis of 4-mercapto-l-lysine derivatives: Potential building blocks for sequential native chemical ligation

Doi:10.1016/j.bmcl.2009.09.107
(2009)

Article Doi

DOI: 10.1021/ja01182a033