REACTION OF o-PHTHALONITRILE WITH ANILINE

DOI: 10.1007/BF00954275

Source and publish data:

Bulletin of the Academy of Sciences of the USSR Division of Chemical Science p. 1588 - 1595 (1983)

Update date:2022-08-04

Topics:

Authors:

Siling, S. A.

Ponomarev, I. I.

Kuznetsov, V. V.

Lokshin, B. V.

Korshak, V. V.

Vinogradova, S. V.

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

Article abstract of DOI:10.1007/BF00954275

Full text of DOI:10.1007/BF00954275

Products guided by the article

Product name:1H-Isoindol-1-imine, 3-phenoxy-

Cas No:60460-27-7

R&D Labs maybe for 60460-27-7

Nanjing distinctions Medical Technology Co., Ltd.(expird)

Contact:+86-15996203785 13914714059

Address:nanjing,jiangsu , China
AllyChem Co., Ltd., Dalian, China（BBChem）

Contact:+86-411-62313318/62313328

Address:No.5 of Jinbin Road, Jinzhou New District, Dalian City, Liaoning Province, P.R.China
Shijiazhuang Frontierchem Co., Ltd.

Contact:+86-311-89271196

Address:4-4-202 No.15 Biandian Street,Shijiazhuang
Yicheng Goto Pharmaceuticals Co.,Ltd.

Contact:+86 710 3423122

Address:5th Floor,East Gate of Building #2,Servo-Industrial Park,1st Qilin Road,Xiangyang,Hubei,China
HANGZHOU PANYU CHEMICAL CO.,LIMITED

Contact:+86-571-86578491

Address:Rm 605, NO.1870 Binsheng Road,Binjiang Dist, Hangzhou, China

Relevant to this article

Doi:10.1246/bcsj.49.779
(1976)
KO^tBu-Promoted Transition-Metal-Free Transamidation of Primary and Tertiary Amides with Amines

Doi:10.1021/acs.orglett.9b02306
(2019)
Kinetics and mechanism of oxidation of aliphatic secondary alcohols by benzyltrimethylammonium chlorobromate

Doi:10.14233/ajchem.2014.16081
(2014)
An efficient TiCl₄-catalysed method for the synthesis of para-substituted aromatic aldehydes

Doi:10.3184/174751915X14408762827272
(2015)
A Concise Synthesis of rac-Ambrox via the Palladium(0)-Catalyzed Carboalkoxylation of an Allylic Ammonium Salt, as Compared to a Formaldehyde Hetero Diels–Alder Approach

Doi:10.1002/hlca.201900097
(2019)
Isolation of enantiomers of a range of tris(bidentate)ruthenium(II) species using chromatographic resolution and stereoretentive synthetic methods

Doi:10.1002/(SICI)1099-0682(199811)1998:11<1677::AID-EJIC1677>3.0.CO;2-S
(1998)

Article Doi