Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/35001
Title: Total synthesis of the proposed structure for itralamide B
Authors: Wang, X
Lv, C
Liu, J
Tang, L
Feng, J
Tang, S
Wang, Z
Liu, Y
Meng, Y
Ye, Tao 
Xu, Z
Keywords: Natural products
Total synthesis
Macrolactonization
Configuration determination
Stereoselectivity
Issue Date: 2014
Publisher: Thieme Medical Publishers
Source: Synlett, 2014, v. 25, no. 7, p. 1014-1018 How to cite?
Journal: Synlett
Abstract: A stereocontrolled total synthesis of the cyclodepsipeptide, itralamide B, has been achieved. Both R- and S-stereoisomers of the side chain were attached to the macrocyclic ring, however, the synthesized structure appears to be different from that of the marine natural product.
URI: http://hdl.handle.net/10397/35001
ISSN: 0936-5214 (print)
1437-2096 (electronic)
DOI: 10.1055/s-0033-1340872
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