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Exact(49)
Synthesis was achieved using the multicomponent Biginelli reaction.
Complex tetracyclic sulfones were designed as γ-secretase inhibitors and a stereoselective synthesis was achieved.
The multi-step synthesis was achieved starting from trimesic acid triethyl ester.
The key step of the synthesis was achieved by employing Suzuki cross-coupling chemistry.
Synthesis was achieved over 12 13 steps in good to excellent yields from multi-gram scale produced mannose donors and acceptors (Supplementary Methods and Supplementary Figs 1–4).
The first-strand cDNA synthesis was achieved by reverse transcription of RNA using random hexamers and SuperScript III Reverse Transcriptase (Invitrogen).
Similar(11)
Fast and efficient synthesis is achieved by DAG-aware rewriting of the AIG.
The EG synthesis is achieved by the reduction of glycoaldehyde derived from serine.
The synthesis is achieved by combining 'living' anionic polymerization, Kumada catalyst-transfer polycondensation, and click chemistry.
Oligo and polysaccharide synthesis is achieved by using other classes of enzymes as catalysts, such as glycosyltransferases, phosphorylases and artificial glycosynthases prepared by mutation of glycosylases.
High rates of glycerol utilization and product synthesis were achieved by simultaneous overexpression of glycerol dehydrogenase (gldA) and dihydroxyacetone kinase (dhaKLM), which are the enzymes responsible for the conversion of glycerol to glycolytic intermediate dihydroxyacetone phosphate.
More suggestions(15)
composition was achieved
synthesis was provided
synthesis was investigated
combination was achieved
synthesis was made
integration was achieved
issues was achieved
synthesis were achieved
synthesis was discussed
synthesis was influenced
synthesis was employed
synthesis was induced
synthesis was conducted
synthesis was estimated
synthesis was observed
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