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- W4297102689 abstract "Three-dimensional organic structures containing sp3 carbons bearing four non-hydrogen substituents can provide drug-like molecules. Although such complex structures are challenging targets in synthetic organic chemistry, efficient synthetic approaches will open a new chemical space for pharmaceutical candidates. This review provides an account of our recent achievements in developing organocatalytic approaches to attractive molecular platforms based on optically active sp3 carbons integrating four different functional groups. These methodologies include asymmetric cycloetherification and cyanation of multifunctional ketones, both of which take advantage of the mild characteristics of organocatalytic activation. Enzyme-like but non-enzymatic organocatalytic systems can be used to precisely manufacture molecules containing complex chiral structures without substrate specificity problems. In addition, these catalytic systems control not only stereoselectivity but also site-selectivity and do not induce side reactions even from substrates with rich functionality." @default.
- W4297102689 created "2022-09-27" @default.
- W4297102689 creator A5033284128 @default.
- W4297102689 creator A5083982624 @default.
- W4297102689 date "2022-09-26" @default.
- W4297102689 modified "2023-09-27" @default.
- W4297102689 title "Organocatalytic Access to Tetrasubstituted Chiral Carbons Integrating Functional Groups" @default.
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- W4297102689 doi "https://doi.org/10.1002/tcr.202200200" @default.
- W4297102689 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/36163471" @default.