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

Anqing World Chemical Co., Ltd.

Contact:+86-556-5800026

Address:Daguan Economic Development Zone of circular economy industrial park Anqing City Anhui province
Shanghai SMEC Trading Co., Ltd.

website:http://www.shanghaismec.com

Contact:+86-21-68811293

Address:ROOM 1101,NO.800 SHANGCHENG RD,SHANGHAI,CHINA
Xi'an caijing Opto-Electrical Science & Technology Co., LTD

Contact:+86-29-88294447

Address:NO.168 Zhangba Rd. East, Xi'an, P.R.China
CHENGDU CHENLV HERB CO.,LTD

Contact:+86-28-88523492

Address:714rooms of Time Square, Pujiang County
Jiangsu Haian Petro chemical Plant

Contact:+86-513-88902723

Address:99, Changjiang West Road, Haian County, Jiangsu

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