2,5-Bis chloromethyl -4-methoxy-1-octoxybenzene (PMOC) is condensed with a starting rotaxane consisting of a bisphenol A salt threaded into β-cyclodextrin (βCD), to lead to a βCD-threaded polyether.
The final ethanol extract was condensed with a rotary evaporator, and the concentrated extract was dried.
Briefly, indole was condensed with a p-phenyl substituted benzaldehyde at pH 2.5 in dilute aqueous acetic acid.
Glyoxylate is condensed with a second molecule of acetyl-CoA to form malate, which is an intermediate of the tricarboxylic acid cycle.
Next, E4P was condensed with a second molecule of DHAP, generating one molecule of sedoheptulose-7-P (S7P) with a GL1-derived carbon atom distributed at S7P4 and the GL3_1-derived carbon backbone distributed at S7P1_3.
It was converted into the corresponding benzoyl chloride 2, which was condensed with a variety of anilines using trimethylamine (TEA) as the base to yield the intermediate compounds 3– 11.
In the serine cycle, Me-THF is condensed with a C2 compound - generated from glyoxylate - to build C3 compounds such as 2-phosphoglycerate and phosphoenolpyruvate (PEP), which are further carboxylated to form oxaloacetate (OAA) and other C4 intermediates.
Further, the overall site layout was condensed with an aim to provide the 'minimum yet adequate' support.
In reductive amination, a ketone or aldehyde is condensed with an amine to form an imine or Schiff base intermediate, which is then reduced to an amine.
To access modifications at the C-terminal tails of histones, a short synthetic peptide bearing the PTM and an N-terminal cysteine is condensed with an α-thioester encompassing the majority of the histone sequence.
Carbon nanohorns (CNHs) functionalized with aryl units, possessing ethylene glycol chains terminated to amine groups, were condensed with modified C60 carrying a free carboxylic acid group.
