Quino[1,2-c]quinazolines. I. Synthesis of quino[1,2-c]quinazolinium derivatives and the related indazolo[2,3-a]quinoline derivatives as analogs of the antitumor benzo[c]phenanthridine alkaloids

DOI: 10.1002/jhet.5570170726

Source and publish data:

Journal of Heterocyclic Chemistry p. 1489 - 1495 (1980)

Update date:2022-08-03

Topics:

Authors:

Phillips

Castle Castle

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

Article abstract of DOI:10.1002/jhet.5570170726

Full text of DOI:10.1002/jhet.5570170726

Products guided by the article

Product name:6-(2-nitro-4,5-dimethoxyphenyl)<1,3>dioxolo<4,5-g>quinoline

Cas No:76787-29-6

R&D Labs maybe for 76787-29-6

TC CHEMICALS CO.,LTD

Contact:0550-7041128 0550-7090578

Address:Wangdian Street,Xinjie Town
XI'AN CHUKANG BIOTECHNOLOGY CO.,LTD

Contact:29-63685658 63685359

Address:Room 3-1202,Building 1,Oriental oasis,East of Xianning Road,Xi'an,Shaanxi 710043 P.R.China
TAIZHOU XINGCHENG CHEMPHARM CO.,LTD.

Contact:0086-0576-88551200,88886292 ,88880039

Address:B Area. 10 Floor.Yaodadasha. 289#.Shifu Road.Taizhou.Zhejiang.China
Shijiazhuang City Xiehe Pharmaceutical Co., Ltd

Contact:+86-311-80817929

Address:Shangzhuang,Shijiazhuang,China
Hangzhou yi lu biont technology Co., LTD

Contact:+86-571-88152630

Address:Hangzhoushi HuafengRoad Yicheng3Building1001room.

Relevant to this article

Short microwave-assisted modular synthesis of naturally occurring oxygenated bibenzyls

Doi:10.1515/znb-2015-0047
(2015)
The relationship between Hirshfeld potential and cytotoxic activity: A study along a series of flavonoid and chromanone derivatives

Doi:10.1107/S205322962000813X
(2020)
Stereoelectronic Influence on the NaBH4 Reduction Stereoselectivity of Alicyclic β-ketoesters

Doi:10.1016/S0040-4039(00)79562-1
(1992)
Transition-State Geometry in the Ene Reactions of Mesoxalic Esters

Doi:10.1021/jo00138a039
(1982)
Mechanistic studies on the biomimetic reduction of tetrahydroxynaphthalene, a key intermediate in melanin biosynthesis

Doi:10.1248/cpb.49.192
(2001)
Doi:10.1021/jo01265a033
(1968)

Article Doi