
Helvetica Chimica Acta p. 2512 - 2518 (1983)
Update date:2022-08-04
Topics:
Fehr, Charles
Intramolecular Grignard-type reaction of the bromolactones 3 and 8 affords the macrocycles 10, 11, 12 and 13, 14, 15, respectively.More efficiently, 10 and 13 are obtaine by intramolecular nucleophilic attack of the carbanions derived from the sulfonyl lactones 20 and 22 and in situ reduction of the intermediate sulfones 21 and 23.The macrocyclic hydroxy ketones 10 and 13 are converted into ExaltoneR (2) muscone(1), respectively.
View Morewebsite:http://www.easchem.com
Contact:+86-731-89722861 89722891
Address:2/F-4/Bld Colorful Palace, No.605 Changsha Ave, Yuhua Area Changsha Hunan China.
Tianjin Tongde Biological Technology Co., Ltd.
Contact:86-22-23309138
Address:Room 402, bulidingE3 Detection certification park, XiQingDistrict, Tianjin City
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
Guangxi Bonger Pharmaceutical Co., Ltd
website:http://napo.lookchem.com/
Contact:+86-18817331185
Address:Donghai Industrial Zone, Tiandong Country,Guangxi,China
Jiaxing Taixin Pharmaceutical Chemical Co., Ltd
Contact:0573-82613601
Address:Chemical Park, Jiaxing, Zhejiang, China
Doi:10.1007/s00044-019-02320-w
(2019)Doi:10.1016/j.bmc.2005.07.024
(2005)Doi:10.1002/1521-3773(20010817)40:16<3012::AID-ANIE3012>3.0.CO;2-Y
(2001)Doi:10.1002/ejic.200400328
(2004)Doi:10.1002/cjoc.201800334
(2018)Doi:10.1021/ol050105c
(2005)