scholarly journals Bench Scale Organic Synthesis Analytical Chemistry

2013 ◽  
Vol 91 (21) ◽  
pp. 47
2018 ◽  
Vol 90 (4) ◽  
pp. 677-702 ◽  
Author(s):  
Jan T. Gozdalik ◽  
Agnieszka Adamczyk-Woźniak ◽  
Andrzej Sporzyński

AbstractRapid development of research on the chemistry of boronic acids is connected with their applications in organic synthesis, analytical chemistry, materials’ chemistry, biology and medicine. In many applications Lewis acidity of boron atoms plays an important role. Special group of arylboronic acids are fluoro-substituted compounds, in which the electron withdrawing character of fluorine atoms influences their properties. The present paper deals with fluoro-substituted boronic acids and their derivatives: esters, benzoxaboroles and boroxines. Properties of these compounds, i.e. acidity, hydrolytic stability, structures in crystals and in solution as well as spectroscopic properties are discussed. In the next part examples of important applications are given.


Author(s):  
Susheel Gulati ◽  
Rajvir Singh ◽  
Suman Sangwan

Heterocycles are unique precursors for the synthesis of various pharmaceuticals and agrochemicals particularly those possessing N- or O- moieties. The development of methods to prepare heterocycles is of great importance in synthesis of organic compounds, especially the heterocycles which can be found in natural products. The synthesis of nitrogen and oxygen containing heterocycles viz. coumarins, dihydropyrimidinones, imidazoles, isoxazoles and benzimidazoles represented an attractive and demanding work for chemists as these nucleus has found extensive applications in several fields such as material science, analytical chemistry and most importantly in medicinal chemistry. Organic synthesis has been attracted towards the development of new environmental friendly procedures to achieve the goals of green chemistry. The fundamental aspects of green chemistry are use of biocatalysts and environmental benign solvents under mild conditions. The present review article summarized the green synthetic methods and biological activities of nitrogen and oxygen containing heterocycles.


ChemInform ◽  
2010 ◽  
Vol 30 (4) ◽  
pp. no-no
Author(s):  
William L. Fitch ◽  
Gary C. Look ◽  
George Detre

2019 ◽  
Author(s):  
Florent Figon ◽  
Thibaut Munsch ◽  
Cécile Croix ◽  
Marie-Claude Viaud-Massuard ◽  
Arnaud Lanoue ◽  
...  

AbstractOmmochromes are widespread pigments that mediate multiple functions in invertebrates. The two main families of ommochromes are ommatins and ommins, which both originate from the kynurenine pathway but differ in their backbone, thereby in their coloration and function. Despite its broad significance, how the structural diversity of ommochromes arises in vivo has remained an open question since their first description. In this study, we combined organic synthesis, analytical chemistry and organelle purification to address this issue. From a set of synthesized ommatins, we derived a fragmentation pattern that helped elucidating the structure of new ommochromes. We identified uncyclized xanthommatin as the elusive biological intermediate that links the kynurenine pathway to the ommatin pathway within ommochromasomes, the ommochrome-producing organelles. Due to its unique structure, we propose that uncyclized xanthommatin functions as a key branching metabolite in the biosynthesis and structural diversification of ommatins and ommins, from insects to cephalopods.


Sign in / Sign up

Export Citation Format

Share Document