Scholarly article on Naphthyl-2-sulfonsaeure- 7394-28-7 from Journal of the Chemical Society C: Organic p. 1390 - 1394

DOI: 10.1039/j39660001390

Source and publish data:

Journal of the Chemical Society C: Organic p. 1390 - 1394 (1966)

Update date:2022-08-03

Topics:

Authors:

Brown,E.J.D.

Harley-Mason,J.

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

Article abstract of DOI:10.1039/j39660001390

Full text of DOI:10.1039/j39660001390

View Article Online / Journal Homepage / Table of Contents for this issue

View Article Online

Products guided by the article

Product name:Naphthyl-2-sulfonsaeure-<2,2-diaethoxycarbonyl-1-(o-nitro-benzoyl)-vinylester>

Cas No:7394-28-7

R&D Labs maybe for 7394-28-7

Xinjiang Zhongtai Chemical Co., Ltd.

Contact:+86-991-8788172

Address:NO.78 XISHAN RD.URUMQI，CHINA
QINGDAO DEVELOP chemistry Co.,Limited

Contact:+86-532-85807910

Address:98#Nanjing Road, Qingdao, China 266071
MS( MAOSHENG )Chemical CO.,LTD

Contact:+86-519-82726678.82726378

Address:TAOXI INDUSTRY ZONE JINTAN
Shanghai agrotree chemical co.,ltd.

Contact:+86-21-50117563

Address:Room 8A,liangfeng building,No.8 dongfang RD.pudong,shanghai,China
Jinan Jinguilin Chemical Co.,Ltd

Contact:+86-531-81188412

Address:3rd floor of Torch Building, Huanyuan Rd, City of Jinan

Relevant to this article

Doi:10.1021/ja01497a028
(1960)
A tungsten-mediated closed cycle of reactivity for the reduction of CO ₂ to CO

Doi:10.1039/c0dt00489h
(2010)
Total synthesis of tricyclic azaspirane derivatives of tyrosine: FR901483 and TAN1251C

Doi:10.1021/ja016030z
(2001)
FeCl₃-Mediated Synthesis of 2-(Trifluoromethyl)quinazolin-4(3 H)-ones from Isatins and Trifluoroacetimidoyl Chlorides

Doi:10.1021/acs.orglett.0c01927
(2020)
New approach to the formation of azepine ring: Synthesis of 2-methyl-6-(5-methyl-2-thienyl)-3H-azepine from 2-methyl-5-propargylthiophene and isothiocyanate

Doi:10.1007/s10593-008-0161-y
(2008)
Biosynthesis of acaterin: Coupling of C₅ unit with octanoate

Doi:10.1021/jo015614g
(2001)

Article Doi

DOI: 10.1039/j39660001390