Tetrahedron Letters p. 4401 - 4404 (1997)
Update date:2022-09-26
Topics: Yield Mass spectrometry (MS) High-performance liquid chromatography (HPLC) Deprotection Protecting group Nuclear Magnetic Resonance (NMR) Purification Macrocyclization Solid-Phase Peptide Synthesis (SPPS) Ring-Closing Metathesis (RCM) Peptide Coupling Aromatic substitution
Roussi, Georges
Zamora, Eduardo Gonzalez
Carbonnelle, Annie-Claude
Beugelmans, Rene
Formation of a biaryl ether bond between the termini of a tetrapeptide containing a highly racemization prone amino acid by the intramolecular SNAr reaction afforded two diastereomeric 16-membered macrocycles along with their respective atropoisomers. The (R,S,R) and its atropoisomer constituted model of chloropeptins I, II, western part.
View MoreHuangshan Violet Biological Technology Co., Ltd
Contact:+86-559-2335676
Address:16-201 JinShanYuan,JiangNan New City,TunXi District,HuangShan City,AnHui Province,China
Ningbo Hi-tech Zone Nice-Synth Chemical Industry Ltd.
Contact:+86-(574)-81110986
Address:No. 1210, Building 3, Wante Business Centre, Hi-tech Zone, Ningbo
Jiangsu Willing Bio-Tech Co ltd
website:http://www.willingbio.com/
Contact:+86 18796908173
Address:No 18 Guoqiao Road
shanghai hekang chemical co.ltd
Contact:021-54173790
Address:328 WuHe Road, Building #A, 2nd Floor, Minhang, Shanghai 201109, China
Kaiping Genuine Biochemical Pharmaceutical Co.,Ltd.
Contact:+86-750-2881198
Address:No.1, Xinke Road, Shatang Town, Kaiping, Guangdong Province, P.R.China
Doi:10.1021/jacs.8b05095
(2018)Doi:10.1021/jo9701804
(1997)Doi:10.1021/ja971658o
(1997)Doi:10.1007/BF01983447
(1997)Doi:10.2174/157017810791824892
(2010)Doi:10.1021/om020130b
(2002)
