A 2000 to 2020 Practitioner’s Guide to Chiral Amine Based Enantioselective Aldol Reactions:Common Ketone Substrates,Best Methods,in Water Reaction Environments,and Defining Nuances

An extensive introduction is provided for the non‐expert regarding enantioselective, amine catalyzed, aldol reactions (Sections 1–3). There, a broad perspective is provided regarding: methodology limitations, mechanism, in‐water versus on‐water definitions and their theoretical basis, small‐ and large‐scale physical‐mechanical aspects, solid versus liquid starting material considerations, reproducibility, ball milling, diketone substrates, etc. The thematic emphasis then turns to practical outcomes for the reaction of nineteen aliphatic, cyclic, and aromatic ketones with 4‐nitrobenzaldehyde and benzaldehyde prior to 2021. In doing so, 172 catalysts are highlighted. The ketone substrates are listed in the Table of Contents (Section 4) and their structures are shown in Figure 1. Each ketone is summarized by a: (i) schematic, (ii) text summary, (iii) catalyst Figures, and (iv) tabular reaction/product data. Individual ketone summaries, at times, represent the distillation of over six hundred and fifty research articles, and the data refinement and its tabular reconstitution is not reproducible using a chemical database search with filters. In the review's broadest use, the Figure 1 ketone structures serve as templates to extrapolate to hypothetical substrates holding more functionality, but of related steric and electronic similarity. This pseudo matching permits a rapid answer to, “Does this methodology suit the ketone substrate at hand or not?” In a positive outcome, the best reaction conditions (stoichiometry, catalyst structure and loading, solvent, time, etc.) to affect aldol product formation (yield, dr, and ee) are delineated. A second envisioned use, allows the directed construction of diketone substrates (after viewing the tabularized data of Section 4) capable of undergoing regioselective mono‐aldol product formation. This ketone regioselectivity tactic, reacting one carbonyl moiety while the other remains unreacted, avoids ketone protection‐deprotection, and is demonstrated for the advantageous synthesis of an Alzheimer drug candidate.