
Tetrahedron Letters p. 5253 - 5256 (1985)
Update date:2022-07-30
Topics:
Vice, Susan F.
Copeland, Catherine R.
Forsey, Steven P.
Dmitrienko, Gary I.
Selective side-chain modification of N-acyl-2,3-dialkylindoles at C-2, effected by bromination with NBS, and at C-3, effected via SN' type reactions of 2,3-dialkyl-2-methoxy-3-methylene indolines generated by low temperature bromination-methanolysis of N-acylindoles, can be usefully applied to the synthesis of substituted pyrrolo<1,2-a> indoles of potential value in the synthesis of mitosene analogs.
View Morewebsite:http://www.alwaychem.com
Contact:+86-532-8586-4000, 8586-5000
Address:NO.51, TAIPING ROAD, QINGDAO, CHINA. 266001
Contact:(86) 731 88718666
Address:Room 1222, Unit 4, Building B, Shangcheng, No.47, Kaiyuan East Road.
Tianjin Te-An Chemtech Co., Ltd.(expird)
Contact:+86-22-65378638
Address:A5-8, No.80 Haiyun Street, TEDA
Shanghai Synmedia Chemical Co., Ltd
Contact:+86-21-38681880
Address:6th Floor, 11A Building, No.528 Ruiqing Road, Heqing town, Pudong new district, Shanghai China
ClickChem Technology Co., Limited
Contact:+86-0310-6519966/0531-52893837
Address:No.750 Shunhua Road, High-Tech Zone, Jinan city, Shandong China
Doi:10.1039/jr9600000473
(1960)Doi:10.1021/jo035100c
(2004)Doi:10.1016/j.tetlet.2011.09.066
(2011)Doi:10.1055/s-1986-31494
(1986)Doi:10.1016/j.jcat.2008.06.028
(2008)Doi:10.1039/jr9620000480
(1962)