Studies on 1,2,3,4-tetrahydroisoquinolines. II. A one-pot synthesis of 1-arylmethyl-1,2,3,4-tetrahydroisoquinolines from an isoquinolinium salt

DOI: 10.1248/cpb.29.1848

Source and publish data:

Chemical and Pharmaceutical Bulletin p. 1848 - 1853 (1981)

Update date:2022-08-02

Topics:

Authors:

Yamada Yamada

Itoh Itoh

Ikezawa Ikezawa

Kiyomoto

Iwakuma Iwakuma

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

Article abstract of DOI:10.1248/cpb.29.1848

Full text of DOI:10.1248/cpb.29.1848

NII-Electronic Library Service

Products guided by the article

Product name:2-benzyl-5,7-dibenzyloxyisoquinolinium bromide

Cas No:76992-46-6

R&D Labs maybe for 76992-46-6

Huangshan Violet Biological Technology Co., Ltd

Contact:+86-559-2335676

Address:16-201 JinShanYuan,JiangNan New City,TunXi District,HuangShan City,AnHui Province,China
Du-Hope International Group

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

Contact:0086-25-52346877

Address:199, Jian Ye Road, Nanjing, China
TC CHEMICALS CO.,LTD

Contact:0550-7041128 0550-7090578

Address:Wangdian Street,Xinjie Town
taicang liyuan chemical co,.ltd

website:http://www.tcliyuanchem.com/productse.php

Contact:86-512-53539583

Address:Room 804,Huaxu Building,No.95,Renmin South Road,Taicang city,Jiangsu Province,China
shanghai meicheng chemical co .,ltd(expird)

Contact:+86-21-50677091

Address:Room 302, Building 7, No.1000, Jinhai Road

Relevant to this article

Substituent Effects on Vinyl Radical Cyclizations onto Aryl Rings

Doi:10.1021/jo971399l
(1998)
Diastereoselective Synthesis of Nitroaldol Derivatives

Doi:10.1002/hlca.19820650402
(1982)
Highly stereoselective radical carbonylations of gem-dihalocyclopropane derivatives with CO

Doi:10.1021/ol062673d
(2007)
NEIGHBOURING GROUP PARTICIPATION IN REACTIONS BETWEEN IODINE AND Ph3Sn(CH2)nS(O)mC6H4Me-p

Doi:10.1016/S0022-328X(00)82446-8
(1981)
REACTION OF 10-FORMYL-3-METHYL-1,2,3,4-TETRAHYDROPYRIMIDO<1,2-a>INDOLE AND ITS DIMETHYLIMINIUM SALT WITH NUCLEOPHILIC AGENTS

Doi:10.1007/BF00514459
(1983)
Alkyl aryl ether bond formation with phenofluor

Doi:10.1002/anie.201500902
(2015)

Article Doi