Studies on quinoline and isoquinoline derivatives. I. Condensation of quinoline and isoquinoline N-oxides with isoxazoles

DOI: 10.1248/cpb.26.2759

Source and publish data:

Chemical and Pharmaceutical Bulletin p. 2759 - 2764 (1978)

Update date:2022-08-04

Topics:

Authors:

Yamanaka

Egawa Egawa

Sakamoto

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

Article abstract of DOI:10.1248/cpb.26.2759

Full text of DOI:10.1248/cpb.26.2759

NII-Electronic Library Service

Products guided by the article

Product name:N-(2-isoquinolin-1-yl-1-methyl-ethyl)-benzamide

Cas No:68764-51-2

R&D Labs maybe for 68764-51-2

Laohekou Jinghong Chemical Co.,Ltd

Contact:+86-0710-3702747

Address:163.East，Huagong Road，Laohekou
Shouguang Nuomeng Chemical Co., Ltd.

Contact:+86-536-5119508/18363669993

Address:Hou Zhen Industrial Park, Shouguang, Shandong, China
Guangzhou PI & PI Biotech Inc. Ltd.

Contact:+86-20-81716320

Address:13th Floor, Xinbao Technology Industrial Park, No. 2 Ruixiang Road, Huangpu District, Guangzhou,Guangdong,China
ZHEJIANG CHEMICAL INDUSTRY INSTITUTE TECHNOLOGY CO.,LTD(expird)

Contact:86-575-82730298

Address:shangyu
ShangHai Ruiyi Medical Technology Co.,Ltd.

Contact:+86-21-54718086

Address:No951 Jianchuan RD，Minhang District

Relevant to this article

Substituted tetralins VI: Tentative assignment of absolute stereochemistry of 1-methyl-1-phenyl-1,2,3,4-tetrahydro-3-naphthoic acid and N,N,1-trimethyl-1-phenyl-1,2,3,4-tetrahydro-3-naphthylamine isomers

Doi:10.1002/jps.2600671009
(1978)
A Surface-Modified Dendrimer Set for Potential Application as Drug Delivery Vehicles: Synthesis, In Vitro Toxicity, and Intracellular Localization

Doi:10.1002/chem.200305386
(2004)
STEREOSELECTIVE SYNTHESIS OF(-)-α-MULTISTRIATIN FROM D-GLUCOSE

Doi:10.1139/v82-050
(1982)
Synthesis, antibacterial activity and docking of 14-membered 9-O-(3-arylalkyl) oxime 11,12-cyclic carbonate ketolides

Doi:10.1016/j.ejmech.2012.10.054
(2013)
Cu-Catalyzed Enantioselective Boron Addition to N-Heteroaryl-Substituted Alkenes

Doi:10.1021/acs.orglett.7b03327
(2017)
Development of unsymmetrical dyads as potent noncarbohydrate-based inhibitors against human β-N-acetyl-D-hexosaminidase

Doi:10.1021/ml300475m
(2013)

Article Doi