Tetrahedron Letters p. 491 - 494 (1996)
Update date:2022-08-03
Topics:
Dai, Jian-Ping
Sodeoka, Mikiko
Shibasaki, Masakatsu
Syntheses of the degradation product 3 of tautomycetin (1) and its diastereoisomers have been achieved. Comparison of the spectral data of these diastereoisomers with those of the degradation product of natural 1 indicates that tautomycetin has the 7R,9S,12S,13S,17S,18R stereochemistry.
View MoreZhuhai Jiacheng Biological Technology Co., Ltd
Contact:0756-8800233
Address:room 222, Lianhua road , Gongbei ,Zhuhai, Guangdong ,China
Wuhan Better Organic Technology Inc.
Contact:13307163183
Address:Wuhan Economic&Technology Development Zone, Hubei
Suqian Ruixing Chemical Co., Ltd.
Contact:+86-527-80805666(总机);84836008(销售)
Address:3 Jingsilu, Zone north, Hubin Xincheng Development Park, Suqian, China
Heliosense Biotechnologies, Inc.
Contact:+86-592-5667290
Address:Xiamen Torch Hi-tech Zone Venture Weiye Building S506
Changsha Nutritopper Bio Technology Co.,Ltd.
Contact:+86-731-87803543
Address:East 1st Street, Baima Road, Ningxiang County
Doi:10.1016/S0040-4039(01)01823-8
(2001)Doi:10.1002/chem.202005438
(2021)Doi:10.1016/S0957-4166(02)00655-9
(2002)Doi:10.1039/jr9520004713
(1952)Doi:10.1080/15533174.2010.492546
(2010)Doi:10.1016/j.reactfunctpolym.2011.07.002
(2011)