INDOLE DERIVATIVES. 133. SYNTHESIS OF 5-(2-PYRIDYL)INDOLE

DOI: 10.1007/BF00633499

Source and publish data:

Chemistry of Heterocyclic Compounds p. 1221 - 1225 (1988)

Update date:2022-08-05

Topics:

Authors:

Akhvlediani, R. N.

Khazhidze, M. M.

Eraksina, V. N.

Suvorov, N. N.

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

Article abstract of DOI:10.1007/BF00633499

Starting from 2-(4-nitrophenyl)pyridine, the product of the Gomberg arylation of pyridine, 5-(2-pyridyl)indole was prepared by the Japp-Klingman reaction. 13C NMR indicated an inductively transmitted interaction between the pyridine and indole rings.

Full text of DOI:10.1007/BF00633499

Products guided by the article

Product name:4-(2-pyridyl)phenylhydrazone ethyl pyruvate anti-isomer

Cas No:121217-71-8

R&D Labs maybe for 121217-71-8

Shanghai Kefu Chemical Co.,Ltd.

Contact:+86-21-34616196

Address:Room601-602, Xuhui Business Building, No.168, Yude Road, Shanghai
Anhui Dexinjia Biopharm Co., Ltd

Contact:+86-531-82375818

Address:9 Hexie Road, kaifaqu, Taihe
Huangshan Violet Biological Technology Co., Ltd

Contact:+86-559-2335676

Address:16-201 JinShanYuan,JiangNan New City,TunXi District,HuangShan City,AnHui Province,China
Beijing ZhongDaXinHe Chemical Product Co.,Ltd(expird)

Contact:010-52876516

Address:tongzhoubeiyuan
Xinxiang Junlong Biological Technology Co., Ltd.

website:https://junlongbio.lookchem.com/

Contact:86-13525059581

Address:Xinxiang City, Henan Province

Relevant to this article

A facile regio- and stereo-selective synthesis of alpha-glycosides of N-acetylneuraminic acid.

Doi:10.1016/0008-6215(88)80035-1
(1988)
A novel method for activation of thioglycosides, combination of N-bromosuccinimide and triflic acid salts

Doi:10.1016/S0040-4039(00)60378-7
(1993)
Production of Adipic Acid from Sugar Beet Residue by Combined Biological and Chemical Catalysis

Doi:10.1002/cctc.201600069
(2016)
Aziridine based electrophilic handle for aspartic acid ligation

Doi:10.1039/c8ob00676h
(2018)
Synthesis, cytotoxic, and carbonic anhydrase inhibitory effects of new 2-(3-(4-methoxyphenyl)-5-(aryl)-4,5-dihydro-1H-pyrazol-1-yl)benzo[d]thiazole derivatives

Doi:10.1002/jhet.3985
(2020)
Quick access to diverse polymerizable molecules (a monomer library) by catalytic [2 + 2 + 2] cycloaddition reactions of functionalized alkynes

Doi:10.1021/ma902792a
(2010)

Article Doi