Reivindicaciones

1. Method for implementing a glyconitrile chemical reaction network, the glyconitrile chemical reaction network being generated from a set of starting compounds comprising (a) glyconitrile; (b) a salt selected from the group consisting of alkali halides, alkaline earth metal halides, or mixtures thereof; and (c) a base selected from the group consisting of alkali hydroxides, alkaline earth metal hydroxides, ammonia, mono alkyl amines, dialkyl amines, trialkyl amines, alkali phosphates, alkaline earth metal phosphates, alkali carbonates, alkaline earth metal carbonates, or mixtures thereof. 2. The method of claim 1, wherein the glyconitrile chemical reaction network further comprises a solvent selected from the group consisting of water, or a combination of water and a water-miscible organic solvent. 3. The method of claim 2, wherein the solvent is water. 4. The method of claim 1, wherein the initial (a) glyconitrile concentration is from 250 mM to 1M, the initial (b) salt concentration is from 100 mM to 1 M, and the initial (c) base concentration is from 30 mM to 750 mM. 5. The method of claim 1, wherein the reaction temperature is chosen from 20-100 °C. 6. A glyconitrile chemical reaction network providing multiple compounds, wherein the glyconitrile chemical reaction network is generated from a set of starting compounds comprising (a) glyconitrile; (b) a salt; and (c) a base, wherein the initial (a) glyconitrile concentration is from 250 mM to 1 M, the initial (b) salt concentration is from 100 mM to 1 M, and the initial (c) base concentration is from 30 mM to 750 mM. 7. The glyconitrile chemical reaction network of claim 6, wherein (b) the salt is selected from the group consisting of alkali halides, alkaline earth metal halides, or mixtures thereof. 8. The glyconitrile chemical reaction network of claim 6, wherein (c) the base is selected from the group consisting of alkali hydroxides, alkaline earth metal hydroxides, ammonia, mono alkyl amines, dialkyl amines, trialkyl amines, alkali phosphates, alkaline earth metal phosphates, alkali carbonates, alkaline earth metal carbonates, or mixtures thereof. 9. The glyconitrile chemical reaction network of claim 6, wherein the glyconitrile chemical reaction network is provided as a solution comprising a solvent selected from the group consisting of water, or a combination of water and a water-miscible organic solvent. 10. The glyconitrile chemical reaction network of claim 6, wherein the temperature of the glyconitrile chemical reaction network is maintained at a temperature selected from the interval between 20 and 100 °C. 11. The glyconitrile chemical reaction network of claim 6, wherein the glyconitrile chemical reaction network is implemented in batch mode or in continuous mode. 12. A method for continuously modulating the glyconitrile chemical reaction network of claim 6 comprising the steps of providing at least one chemical input by means for a continuous reaction system having at least one inlet channel, analysing the composition of the glyconitrile chemical reaction network by means for analysis, and varying one or more chemical reaction conditions selected from the group of temperature, agitation speed, pH, reagent concentration, or reaction time. 13. A process for preparing amino acids, nucleobases, nucleotides, oligopeptides, and/or metabolite derivatives thereof using a glyconitrile chemical reaction network according to any of the preceding claims, comprising the steps of generating and/or implementing a glyconitrile chemical reaction network, analysing the composition of the glyconitrile chemical reaction network after a defined set time, identifying a desired amino acid, nucleobase, nucleotide, oligopeptide, and/or metabolite derivative thereof, and modulating the reaction conditions in a way to predominately produce the desired amino acid, nucleobase, nucleotide, oligopeptide, and/or metabolite derivative thereof. 14. Use of the glyconitrile chemical reaction network of claim 6 or implemented according to claim 1 for a multi-compound screening of biologically active substances. 15. A device configured for implementing a glyconitrile chemical reaction network of claim 1 or claim 6 comprising (i) means for the preparation of the glyconitrile chemical reaction network, (ii) means for sampling the glyconitrile chemical reaction network composition one or more times at defined time points providing one or more sample datasets, (iii) means for analysing the one or more sample datasets, including means for data acquisition and data extraction, providing one or more analysis datasets, (iv) means for data processing of the obtained one or more analysis datasets, and (v) means for compounds identification.