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Computer-Guided total synthesis of natural products. Recent examples and future perspectives
Quantum chemical calculations of nuclear magnetic resonance (NMR) shifts and coupling constants have been extensively employed in recent years mainly to facilitate structural elucidation of organic molecules. When the results of such calculations are used to determine the most likely structure of a natural product in advance, guiding the subsequent synthetic work, the term ?computer-guided synthesis? could be coined. This review article describes the most relevant examples from recent literature, highlighting the scope and limitations of this merged computational/experimental approach as well.
Because enzymes can increase reaction rates by enormous factors and tend to be very specific, Quality Control of (S)-4-Isopropylthiazolidine-2-thione, typically producing only a single product in quantitative yield, they are the focus of active research.you can also check out more blogs about Quality Control of (S)-4-Isopropylthiazolidine-2-thione
Reference：
Quinuclidine – Wikipedia,
Quinuclidine | C7H724N | ChemSpider