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 MoreChemsky（shanghai）International Co.,Ltd.
Contact:0
Address:0
Contact:+86-533-3112891
Address:zibo
Lishui Nanming Chemical Co., Ltd(expird)
Contact:+86-0578-2134101，2697830
Address:No.19 Tongji Road Shuige Industrial zone
Contact:0571-
Address:zhejing
Shanghai shibo Chemical Co., Ltd
Contact:+86-021-60753516
Address:688 Qiushi Road, Jinshan High-tech Park, Shanghai, China,201512
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)
