Formation of 6,13dimethyl-5,12-diazachrysene by oxidative coupling of 2- methylindole followed by base-induced ring-expansion

DOI: 10.1016/S0040-4039(98)00670-4

Source and publish data:

Tetrahedron Letters p. 4119 - 4122 (1998)

Update date:2022-08-31

Topics:

Authors:

Bergman Bergman

Lindstroem

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

Article abstract of DOI:10.1016/S0040-4039(98)00670-4

Oxidative coupling of 2-methylindole with FeCl₃ gave, in addition to a trimeric coupling product, also the ring-expanded product 6,13-dimethyl- 5,12-diazachrysene.

Full text of DOI:10.1016/S0040-4039(98)00670-4

Products guided by the article

Product name:Dibenzo[c,h][2,6]naphthyridine

Cas No:218-30-4

R&D Labs maybe for 218-30-4

Hangzhou innopharma technology Co,.Ltd.(expird)

Contact:+86-13388601988

Address:Room845,lixin building, moganshan road, hangzhou, china
shanghai meicheng chemical co .,ltd(expird)

Contact:+86-21-50677091

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

Contact:(1) 206-3550089

Address:5115 NE 8TH PL, Renton, WA 98059 USA
LIDE PHARMACEUTICALS LIMITED

website:http://www.lidepharma.com

Contact:+86-25-58409506

Address:11F, Building A1, No.288 North Zhongshan Road, Gulou District, Nanjing,210003, P.R.China.
MOKESI TECHNOLOGY CO., LIMITED

Contact:000000000000

Address:NO.168 ,Weisi Road, Zhengzhou City,Henan,China

Relevant to this article

Doi:10.1007/BF00781204
()
Facile Fabrication of Ultrasmall Copper Species Confined in Mesoporous Silica for Chemo-Selective and Stable Hydrogenation Ethylene Carbonate Derived from CO₂

Doi:10.1002/cctc.201800828
(2018)
Palladium(II)/Cationic 2,2'-Bipyridyl system as a highly efficient and reusable catalyst for the Mizoroki-Heck reaction in water

Doi:10.3390/molecules15010315
(2010)
Elastic and inelastic electron tunneling spectroscopy of a new rectifying monolayer

Doi:10.1021/ja068729g
(2007)
Mono- and dialkylborane reagents from silylamine-boranes

Doi:10.1016/S0040-4039(98)01262-3
(1998)
A Diels-Alder/retro-Diels-Alder approach for the enantioselective synthesis of microbial butenolides

Doi:10.1002/ejoc.201200991
(2012)

Article Doi