Functionalized compounds, which are difficult to produce by classical chemical synthesis, are of special interest as biotechnologically available targets. They represent useful building blocks for subsequent organic syntheses, wherein they can undergo stereoselective or regioselective reactions. "White Biotechnology" (as defined by the European Chemical Industry [ http://www.europabio.org/white_biotech.htm ], as part of a sustainable "Green Chemistry,") supports new applications of chemicals produced via biotechnology. Environmental aspects of this interdisciplinary combination include: Use of renewable feedstock Optimization of biotechnological processes by means of: New "high performance" microorganisms On-line measurement of substrates and products in bioreactors Alternative product isolation, resulting in higher yields, and lower energy demand In this overview we describe biotechnologically produced pyruvic, 2-oxopentaric and 2-oxohexaric acids as promising new building blocks for synthetic chemistry. In the first part, the microbial formation of 2-oxocarboxylic acids (2-OCAs) in general, and optimization of the fermentation steps required to form pyruvic acid, 2-oxoglutaric acid, and 2-oxo-D-gluconic acid are described, highlighting the fundamental advantages in comparison to chemical syntheses. In the second part, a set of chemical formula schemes demonstrate that 2-OCAs are applicable as building blocks in the chemical synthesis of, e.g., hydrophilic triazines, spiro-connected heterocycles, benzotriazines, and pyranoic amino acids. Finally, some perspectives are discussed.

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The condensation reactions of the structurally similar monomers 1,3-phenylenediamine (1a) and 2,6-diaminopyridine (1b) with N,N-carbonyldiimidazole have been compared. Whereas the reaction of 1a resulted in an amino terminated oligomeric polyurea, a mixture of two macrocyclic trimers and one macrocyclic tetramer was obtained in the case of 1b. The three components of the mixture could be isolated by extraction with DMSO at different temperatures. The structure of the macrocyclic compounds was investigated by means of NMR and matrix-assisted laser desorption/ionization time-of-flight mass spectroscopy.

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Synthesis of 1,2,4‐Benzotriazine‐3‐acetates and ‐acetamides Substituted 1,2,4‐benzotriazine‐3‐acetates 6 are prepared by the reduction of (2‐nitrophenyl)hydrazonoethers 4 or (2‐nitrophenyl)amidrazones 5. The 1,2,4‐benzotriazin‐3‐ylacet‐anilid 9g forms a yellow azomethine dye 10 by oxidative coupling with N,N‐diethyl‐p‐phenylenediamine.

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2,