AHFC promoted the decomposition of protein to form heterocycle compounds in the resulting cake according to in situ FTIR results.
2
A series of pleuromutilins modified by introduction of a boron-containing heterocycle on C(14) of the polycyclic core are described.
3
Structure-activity studies demonstrate the requirement for the core heterocycle in addition to an optimal 2,6-disubstituted aniline group.
4
Previous works in our laboratories established the bioisosteric equivalency of the indole heterocycle and naphthalene in a series of melatonin receptor ligands.
5
The possible reaction pathway of N-heterocycle compounds formation from cellulose during hydrothermal liquefaction with NH 3 ·H 2 O was proposed.
6
The reactivity, synthesis, and structure of the mesoionic 3-substituted-1,2,3,4-oxatriazole derivatives described here provide interesting new information on this known but poorly understood heterocycle.
7
Their activity has been related to the nature of the added heterocycles.
8
This is the first report on the hydrothermal generation of two fused heterocycles.
9
Further manipulation of the dihydropyrimidone skeleton gives access to unique heterocycles.
10
A number of interesting points regarding the chemistry of medium-ring oxygen heterocycles are highlighted.
11
This enables rapid and reliable regioselectivity prediction for radical C-H bond functionalization of heterocycles.
12
Vinyl azides are highly versatile synthons that provide access to numerous N-heterocycles and other functional groups.
13
Results: Shape and electrostatic similarity matching was used to select five-membered heterocycles to replace the ethyl ester functionality.
14
The heterocycles and their mixture displayed efficient solvent dependent fluorescence in the visible region of the solar spectrum.
15
These results suggest that thiadiazole urea heterocycles which incorporate a substituted phenylalanine can provide selective inhibitors of stromelysin.
16
The enzymes aldehyde oxidase and xanthine oxidase catalyze the oxidation of a wide range of N-heterocycles and aldehydes.