Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/27410
Title: First total synthesis and stereochemical revision of Laxaphycin B and its extension to Lyngbyacyclamide A
Authors: Boyaud, F
Mahiout, Z
Lenoir, C
Tang, S
Wdzieczak-Bakala, J
Witczak, A
Bonnard, I
Banaigs, B
Ye, T 
Inguimbert, N
Issue Date: 2013
Publisher: American Chemical Society
Source: Organic letters, 2013, v. 15, no. 15, p. 3898-3901 How to cite?
Journal: Organic letters 
Abstract: The first total synthesis of laxaphycin B was accomplished through stepwise automated Solid Phase Peptide Synthesis (SPPS), leading to the structural revision of its stereochemistry especially with regard to the configuration of one of the two 3-hydroxyleucines of this cyclic dodecapeptide of marine origin. The analogous Lyngbyacyclamide A was obtained by an extension of this synthesis.
URI: http://hdl.handle.net/10397/27410
ISSN: 1523-7060
EISSN: 1523-7052
DOI: 10.1021/ol401645m
Appears in Collections:Journal/Magazine Article

Access
View full-text via PolyU eLinks SFX Query
Show full item record

SCOPUSTM   
Citations

13
Last Week
0
Last month
0
Citations as of Aug 20, 2017

WEB OF SCIENCETM
Citations

15
Last Week
0
Last month
1
Citations as of Aug 20, 2017

Page view(s)

28
Last Week
2
Last month
Checked on Aug 20, 2017

Google ScholarTM

Check

Altmetric



Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.