Aminomethylation in system of phenylacetonitril

DOI: 10.1002/ardp.19683011202

Source and publish data:

Archiv der Pharmazie und Berichte der Deutschen Pharmazeutischen Gesellschaft p. 881 - 896 (1968)

Update date:2022-08-16

Topics:

Authors:

Kreutzberger

Abel Abel

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

Article abstract of DOI:10.1002/ardp.19683011202

Full text of DOI:10.1002/ardp.19683011202

Products guided by the article

Product name:1.1.3.3-Tetra-(4-nitro-phenyl)-propen-⁽¹⁾

Cas No:21419-04-5

R&D Labs maybe for 21419-04-5

Jingzhou TianHe Sci&Tech Chemical Co., Ltd.

Contact:86-716-8331612

Address:Jiangjin Road, #18, High-grade technology industries development district, Jingzhou city, Hubei province
Zipont chem(wuhan）Tech co.，Ltd

Contact:+86-27-87587198

Address:wuhan
ORCHID CHEMICAL SUPPLIES LTD

website:http://www.orchid-chem.com

Contact:+86-571-85395792

Address:607, North Zhongshan Road, Hangzhou 310000 China
Liaoyang Xinyou Chemical Products Co.,Ltd.

Contact:+86-419-5165433 13604191870

Address:Huishang Road6-1, Hongwei District, Liaoyang, Liaoning, China
Wuhan Chemchemical Co., Ltd.(expird)

Contact:15973022782

Address:7-5-6218,Incubation Centre,Guandong Industry Park, East Lake High-Tech Development Zone,Wuhan City.

Relevant to this article

Synthesis of N-methyl secondary amines

Doi:10.1081/SCC-120018703
(2003)
Synthesis of 4-aryl-5-nitro-1,2,3-triazoles

Doi:10.1023/B:RUJO.0000036090.61432.18
(2004)
Steric and Conformational Effects in Nicotine Chemistry

Doi:10.1021/jo00328a010
(1981)
Use of acid-labile protective groups for carbohydrate moieties in synthesis of glycopeptides related to type II collagen

Doi:10.1016/S0040-4020(98)83057-3
(1998)
An efficient and large-scale enantioselective synthesis of PNP405: A purine nucleoside phosphorylase inhibitor

Doi:10.1021/jo020256i
(2002)
Ligand-, base-, co-catalyst-free copper fluorapatite (CuFAP) as a versatile, ecofriendly, heterogeneous and reusable catalyst for an efficient homocoupling of arylboronic acid at ambient reaction conditions

Doi:10.1039/c4ra16760k
(2015)

Article Doi