Synthesis of 4-amino[1]benzofuro[3,2-g]cinnolines

DOI: 10.1002/jhet.5570170607

Source and publish data:

Journal of Heterocyclic Chemistry p. 1189 - 1193 (1980)

Update date:2022-08-04

Topics:

Authors:

Laduree Laduree

Florentin

Robba Robba

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

Article abstract of DOI:10.1002/jhet.5570170607

Full text of DOI:10.1002/jhet.5570170607

Products guided by the article

Product name:3-(propan-2-yl)[1]benzofuro[3,2-g]cinnolin-4-amine

Cas No:76795-58-9

R&D Labs maybe for 76795-58-9

Shandong united-rising pharmaceutical cooperation.,ltd.

Contact:008653187965009

Address:171No., Jing5 Road, Shizhong District, Jinan, China
Shenzhen Feiming Science and Technology Co,. Ltd

Contact:+86-755-85232577

Address:#B2309, Fenglin International Center ,Jixiang Road, Longcheng street, LongGang District, Shenzhen city, Guangdong province, China.
Beijing Wisdom Chemicals Co., Ltd.

Contact:+86-10-52350335

Address:F2, BLDG 19, Liando Valley U, Majuqiao, Tongzhou District, Beijing, China
Beijing Green Guardee Technology CO,.LTD

Contact:+86-10-69706062

Address:F2 BLdj,5 No.37 Chaoqian Road
Wuxi Olite Chemical Co., Ltd.

Contact:86-510-82853889

Address:Rm.3732, No.18-2,Yonghe Rd.,Wuxi,Jiangsu,214023,China

Relevant to this article

A supramolecular optic sensor for selective recognition AMP

Doi:10.1016/j.inoche.2010.04.006
(2010)
A practical formal synthesis of camptothecin

Doi:10.1016/j.tetlet.2007.07.017
(2007)
DIRECT CONVERSION OF D-GLUCOSAMINE INTO D-GULOSAMINE

Doi:10.1016/S0008-6215(00)90783-3
(1984)
Synthesis of γ-Lactams by Formal Cycloadditions with Ketenes

Doi:10.1021/acs.orglett.1c00335
(2021)
A convenient procedure for the synthesis of nonsymmetrical bivalent selective serotonin reuptake inhibitors using polymer-supported reagents

Doi:10.1016/S0960-894X(00)00576-X
(2000)
Imidazolium chloride-Co(iii) complex immobilized on Fe₃O₄@SiO₂ as a highly active bifunctional nanocatalyst for the copper-, phosphine-, and base-free Heck and Sonogashira reactions

Doi:10.1039/c8gc03919d
(2019)

Article Doi