Stereoselective synthesis of an eleganine A core

2020 ◽  
Vol 18 (24) ◽  
pp. 4566-4568
Author(s):  
Gints Smits ◽  
Ronalds Zemribo

The core structure of eleganine A – a cytotoxic indole monoterpene alkaloid – was accessed for the first time.

2019 ◽  
Vol 7 (11) ◽  
pp. 3226-3230 ◽  
Author(s):  
Linna Zhu ◽  
Jing Xu ◽  
Yahan Shan ◽  
Cheng Zhong ◽  
Xiaosheng Tang ◽  
...  

For the first time, dipyridyl ketone and benzophenone were used as the core structure to synthesize new hole transport materials.


ChemInform ◽  
2010 ◽  
Vol 28 (50) ◽  
pp. no-no
Author(s):  
H. ZHANG ◽  
Y. WANG ◽  
R. THUERMER ◽  
M. MEISENBACH ◽  
W. VOELTER

1997 ◽  
Vol 1997 (9) ◽  
pp. 1871-1876 ◽  
Author(s):  
Hong Zhang ◽  
Yali Wang ◽  
René Thürmer ◽  
Mark Meisenbach ◽  
Wolfgang Voelter

2002 ◽  
Vol 55 (2) ◽  
pp. 61 ◽  
Author(s):  
E. Vinogradov ◽  
Z. Sidorczyk ◽  
Y. A. Knirel

The lipopolysaccharide (LPS) core structure was studied in seven rough strains of Proteus and 26 smooth strains belonging to various Proteus O-serogroups. All LPSs share a common heptasaccharide fragment, which includes two Kdo, three Hep, one Glc, and one GalA residue. Core structures differ between strains and within each strain in the presence of a variety of additional monosaccharides and non-sugar substituents. In many strains, the LPS includes a cyclic acetal of GalNAc in the open-chain form, which builds up a new type of linkage between monosaccharides. The covalent linkage of aliphatic polyamines, e.g. putrescine and spermidine, to the LPS was confirmed for the first time and the location of the amines at the carboxyl group of a GalA residue established. Analyses revealed peculiar features of the core structure, which are characteristic of P. mirabilis on one hand and P. vulgaris and P. penneri on the other hand.


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