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 MoreWuxi Forest Biological Co.,Ltd
Contact:+86-510-81602300
Address:Room 317,Building D, No.159 middle Chengjiang Road,Jiangyin Wuxi city.
Contact:+86+21-58956006 15800617331
Address:402 Room, 150# Cailun Road, Zhangjiang high tech park, Shanghai
Zhejiang Sucon Silicone Co.,Ltd
Contact:+86-575-88046692
Address:Qisheng Rd., Paojiang Industrial Zone, Shaoxing, Zhejiang, China.
website:http://www.josunpharma.com
Contact:+86-311-80715268 80766839
Address:No.39, Zhaiying Street, Shijaizhuang,Hebei,China
Global United Biotechnology Inc.
Contact:+86-21-61618568
Address:Room 309, Building 6, NO.135, Jinyu Road, Pudong
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)
