Scholarly article on 3309-53-3 from Journal of the American Chemical Society p. 4686,4689

DOI: 10.1021/ja01574a029

Source and publish data:

Journal of the American Chemical Society p. 4686,4689 (1957)

Update date:2022-08-02

Topics:

Authors:

McKay McKay

Albertson

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

Article abstract of DOI:10.1021/ja01574a029

Full text of DOI:10.1021/ja01574a029

Products guided by the article

Product name:

Cas No:3309-53-3

R&D Labs maybe for 3309-53-3

Hubei Onward Bio-Development Co., Ltd.

Contact:+86-718-8417012

Address:No.517,Shizhou Avenue,Enshi City,Hubei Province,China,445002
MTT Pharma & Bio-technology Co.,Ltd(expird)

Contact:+86-21-58407925

Address:Room2019, Building C, Tomson Center, No.158, Zhang Yang Road, Shanghai, China
Improve Medical Technology(Nanxiong) Co., Ltd

Contact:86-751-3836997

Address:No.33, Pingan First Road, Fine Chemical Industry Base, Nanxiong City, Shaoguan, Guangdong, China
Zhenjiang Huayu I/E Co.,LTD

Contact:86-511-85210668 0511-85210668, 85210818, 85210898

Address:Yihai Garden E-902,NO.99 Daxi RD., Zhenjiang Jiiangsu ,China
enantiotech corporation ltd

Contact:+86-0760-85282375

Address:zhongjing road,zhongshan torch hi-tech industrial development zone

Relevant to this article

Synthesis, characterisation and electrochemical behaviour of rhodium(III) complexes containing 1,2-naphthoquiaone-2-oxime and formation of imine complexes through N - O bond cleavage

Doi:10.1002/1099-0682(200102)2001:2<511::AID-EJIC511>3.0.CO;2-U
(2001)
A simple and efficient route to substituted 2-alkylsulfanyl-6-oxo-1,4,5,6- tetrahydropyridine-3-carbonitriles

Doi:10.1134/S1070428006120256
(2006)
An electron rich porous extended framework as a heterogeneous catalyst for Diels-Alder reactions

Doi:10.1039/c3cc43681k
(2013)
Novel 3',5'-cyclic nucleotide analogue: adenosine 3',5'-cyclic boranomonophosphate.

Doi:10.1021/ol0003230
(2001)
Synthesis and insecticidal evaluation of tetrahydroimidazo[1,2-a]pyridin-5(1H)-one derivatives

Doi:10.1016/j.cclet.2015.10.002
(2016)
Mizoroki–Heck reaction of 1,2-disubstituted aryl alkenes: Variables of synthesis, solvent and ligand modulation of reactivity

Doi:10.1080/00397911.2020.1811986
(2020)

Article Doi

DOI: 10.1021/ja01574a029