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. Author manuscript; available in PMC: 2023 Mar 8.
Published in final edited form as: Acc Chem Res. 2021 Feb 12;54(5):1157–1167. doi: 10.1021/acs.accounts.0c00791

Figure 5.

Figure 5.

Conceptualization of both static and dynamic retrosynthetic analysis as movement through chemical space. A. Viewing NPs as clusters of related structures in chemical space; B. Viewing the relationships between nodes as transforms (Tf.); C. As in traditional retrosynthetic analysis, a Tf. can alter retrosynthetic paths. D. Dynamic analysis constrains the transform by function rather than reactivity.