Scholarly article on N-phenyl-selenobenzamide 57767-71-2 from Journal of the Chemical Society. Chemical communications p. 617 - 618

DOI: 10.1039/c39750000617

Source and publish data:

Journal of the Chemical Society. Chemical communications p. 617 - 618 (1975)

Update date:2022-08-16

Topics:

Authors:

Cava,M.P.

Saris,L.E.

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

Article abstract of DOI:10.1039/c39750000617

Full text of DOI:10.1039/c39750000617

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

View Article Online

Products guided by the article

Product name:N-phenyl-selenobenzamide

Cas No:57767-71-2

R&D Labs maybe for 57767-71-2

Beijing Century Richap Chemistry Co.,Ltd

Contact:+86- 010-64455497

Address:Guannan County, Lianyungang City, Jiangsu Province, China
Hefei Highzone Fine Chemical S&T CO.,LTD

Contact:86-0551-63663560

Address:room 1801 NO. 24 Shuguang RD.
Xi'an North Information Industry Co., Ltd. Weilv Chemical Department

Contact:+86-29-88156413

Address:Jixiang Road 99 Xi'an Shaanxi Province
TIANJIN DONGRUXIANG MINERALS MARKETING CO.,LTD(expird)

Contact:22-58516360

Address:tianjin
TAIXING BEST NEW MATERIALS CO., LTD

Contact:0523-87998158;

Address:No.18 Zhonggang Road，Taixing City ，Jiangsu , China

Relevant to this article

Synthesis of Cyclopropane Fatty Acids by C(sp³)?C(sp³) Cross-Coupling Reaction and Formal Synthesis of α-Mycolic Acid

Doi:10.1002/adsc.201800901
(2018)
Efficient enantioselective total synthesis of (-)-epipodophyllotoxin

Doi:10.1002/anie.200351086
(2003)
Synthesis of N-acetyl-DL-glutamic acid 5-dimethylaminoethyl ester.

Doi:10.1002/jps.2600580729
(1969)
Design and synthesis of dihydrofolate reductase inhibitors encompassing a bridging ester group. Evaluation in a mouse colitis model

Doi:10.1021/jm021062y
(2003)
Discovery of 5-(3-bromo-2-(2,3-dibromo-4,5-dimethoxybenzyl)-4,5-dimethoxybenzylidene)thiazolidine-2,4-dione as a novel potent protein tyrosine phosphatase 1B inhibitor with antidiabetic properties

Doi:10.1016/j.bioorg.2021.104648
(2021)
New β lactam antibiotics. Functionalisation of the cephem 3 position with sulfur or nitrogen bearing substituents

Doi:10.1002/hlca.19750580824
(1975)

Article Doi

DOI: 10.1039/c39750000617