Tetrahedron Asymmetry p. 137 - 140 (1990)
Update date:2022-08-04
Topics: Yield Catalyst Enantioselective Total synthesis Stereoselective Protecting group Chiral Auxiliary Functional Group Interconversion Spectroscopic Analysis (+)-Asperlin
Ramesh
Franck
A stereochemically unambiguous synthesis of (+)-asperlin from L-rhamnose establishes the configuration of the antibiotic as 4S, 5S, 6S, 7R.
View MoreContact:+86-571-28186845
Address:Room 1224,Eastcom Mansion,398 Wensan Road,Hangzhou,310013 China
Zhejiang Allied Chemical Co.,Ltd
Contact:18967038207
Address:Area A-30, High-tech Industrial Park, Quzhou, Zhejiang, China.
website:http://www.herbpurify.com
Contact:0086-028-85249238
Address:Room709-C1,Incubator Building, Tianfu Life Science Park No.88,Keyuan Road,Gaoxin district,Chengdu City,Sichuan Prov,China
Haitong Chemical Industrial Co.,Ltd.
website:https://www.haitonglongwin.com/
Contact:+86-022-66221018
Address:18-701, No.99, The 4th Street, TEDA,
Zhejiang Sucon Silicone Co.,Ltd
Contact:+86-575-88046692
Address:Qisheng Rd., Paojiang Industrial Zone, Shaoxing, Zhejiang, China.
Doi:10.1039/c39870000877
(1987)Doi:10.1021/acs.orglett.0c00681
(2020)Doi:10.1039/b810414j
(2009)Doi:10.1002/ejic.200701098
(2008)Doi:10.1016/j.jorganchem.2007.01.002
(2007)Doi:10.1080/00222890109601919
(1955)
