
Journal of Organic Chemistry p. 1471 - 1475 (1990)
Update date:2022-08-05
Topics: Synthesis Characterization Yield Novel Purification Reaction Conditions Preparation 4-substituted
Khanapure, Subhash P.
Biehl, Edward R.
The title compounds 20, 21, and 22 have been prepared in modest yields by a two-step reaction involving first the reaction of bromoarenes 3, 7, and 8 with lithioalkyl- and lithioarylacetonitriles under aryne-forming conditions.The cyano products 10, 14, and 16 so formed were then converted to the corresponding isochroman-3-ones by acidic hydrolysis.
View MoreJIAXING SUNS INTERNATIONAL TRADE CO LTD
Contact:18367306858
Address:No.123,Huixin Avenue,Huimin Dist
Shanghai Coupling Pharmaceutical R&D Co., Ltd.(expird)
Contact:+86 021 50106671
Address:403 Room No.4 Buiding, No. 526 Ruiqing Road, Shanghai Zhangjiang Hi-Tech Park
Shanghai ZaiQi Bio-Tech Co., Ltd.,
Contact:+86-21-5482 4098
Address:Bldg. No.7, No.201 MinYi Rd,Songjiang CaoHeJing High-Tech Park Shanghai 201516 P,R,China
taicang liyuan chemical co,.ltd
website:http://www.tcliyuanchem.com/productse.php
Contact:86-512-53539583
Address:Room 804,Huaxu Building,No.95,Renmin South Road,Taicang city,Jiangsu Province,China
Shandong Topscience Biotech Co., Ltd.
Contact:0633-2619278
Address:No. 98 Lanshan West Road, Lanshan District, Rizhao, Shandong Province, P.R. of China
Doi:10.3184/030823410X12747104952034
(2010)Doi:10.1016/j.tet.2010.06.081
(2010)Doi:10.1016/j.bmcl.2010.07.001
(2010)Doi:10.1002/ejoc.201000558
(2010)Doi:10.1021/om030629l
(2004)Doi:10.1055/s-1994-25609
(1994)