Journal of Organic Chemistry p. 731 - 733 (1984)
Update date:2022-08-05
Topics:
Kurth, Mark J.
Burns, Dennis H.
O'Brien, Michael J.
An efficient , stereoselective synthesis of octahydro-as-indacenone 2 , the carbocycle fragment of the antibiotic ikarugamycin , is described.The prominent step in the sequence is an intramolecular Diels-Alder reaction, which establishes the relative stereochemistry of 2.
View MoreShanghai Dano Pharmaceutical Co.,Ld.(expird)
Contact:+86-592-6266840
Address:Building 1 Room 512, 720 Cailun Rd, Zhangjiang High-Tech Park, Shanghai 201203, China
TIANJIN FESTO CHEMICAL CO.,LTD(expird)
Contact:86-22-25814570
Address:No.12th,5th Ave.,TEDA,Tianjin,China
Contact:0086-27-83607103/83642615
Address:No.498, Jianshe Ave, Wuhan, China
Contact:+86-20-32051076
Address:1105,Building A, International Business Incubator,Science City
Shanghai PengMo Biotechnology Co.,Ltd
website:http://www.pengmobio.lookchem.com
Contact:86-13052359378
Address:No.218 Hai Qu Road.Shanghai.China
Doi:10.1021/ja0609708
(2006)Doi:10.1055/s-2006-926283
(2006)Doi:10.1016/j.ica.2005.12.077
(2006)Doi:10.1055/s-0033-1338860
(2013)Doi:10.1016/0008-6215(83)84006-3
(1983)Doi:10.1039/b513944a
(2006)
