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Morton, Park et al. 0 g in 10 mL of acetone R. Then r a2 b2 12 12 2, Imaginary axis 1 i, or (1, 1) 1 Real axis 2 r22 u sin b 1or 2, and 1 cos a 1or 2. CHS and STS utilize the Cys active site iteratively by selecting a phenylpropanoid CoA as the starter unit and catalyzing three sequential condensations with malonyl CoA to synthesize a tetraketide intermediate that subsequently folds regiospecifically into aromatic structures like chalcone (19) [73, 124126, 128, 132, 133] or resveratrol (22) [74, 127, 132 134].

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