The Reductive Potential of Dodecacarbonyltri-iron on Basic Alumina

DOI: 10.1039/c39800000821

Source and publish data:

Journal of the Chemical Society. Chemical communications p. 821 (1980)

Update date:2022-08-16

Topics:

Authors:

Alper, Howard

Gopal, Madhuban

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

Article abstract of DOI:10.1039/c39800000821

Dodecacarbonyltri-iron on basic alumina constitutes a simple, mild, and convenient method for reducing nitroarenes to aromatic amines.

Full text of DOI:10.1039/c39800000821

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

Products guided by the article

Product name:p-Anisidine

Cas No:104-94-9

R&D Labs maybe for 104-94-9

Taizhou Elitechemie MediPharma Technology Co.,Ltd.

Contact:+86-523-86810021

Address:Building G14,NO.1 Avenue,China Medical City, Taizhou, Jiangsu,China
Jiaxing Barton Chemicals

website:http://www.chinabarton.com

Contact:+86-573-82719618

Address:No. 162 Fumin Road, Honghe Town,
TAIXING BEST NEW MATERIALS CO., LTD

Contact:0523-87998158;

Address:No.18 Zhonggang Road，Taixing City ，Jiangsu , China
Wuhan Better Organic Technology Inc.

Contact:13307163183

Address:Wuhan Economic&Technology Development Zone, Hubei
Shenyang Xingzhenghe Chemical Co., Ltd.

Contact:024-23509232

Address:No. 33, Naner Road, Heping Dist.

Relevant to this article

Visible light-controlled carbon monoxide delivery combined with the inhibitory activity of histone deacetylases from a manganese complex for an enhanced antitumor therapy

Doi:10.1016/j.jinorgbio.2021.111354
(2021)
A new synthetic methodology for tiazofurin

Doi:10.1081/NCN-100002548
(2001)
Easy Access to Crystalline Indolines via Hydrogen Bond Transfer

Doi:10.1002/jhet.3516
(2019)
Batch to flow deoxygenation using visible light photoredox catalysis

Doi:10.1039/c2cc37206a
(2013)
Doi:10.1021/ja01160a010
(1950)
Pseudomonas cepacia lipase immobilized onto chitosan-coated activated carbon: An efficient catalyst for transesterification enantiomer resolution of (R,S)-1-Phenyl-3-buten-1-ol

Doi:10.14233/ajchem.2014.18170
(2014)

Article Doi