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- W4313347103 abstract "Five-membered carbo- and heterocycles are ubiquitous in a variety of pharmacological agents and natural products. The recent decades have witnessed the exuberant development of cornucopias of (3 + 2) cycloaddition reactions, in particular via the means of nucleophilic organocatalysis, in a highly asymmetric fashion, to construct chiral five-membered rings showcasing novel substrate activation modes. With global concerted efforts, dedicated libraries of nucleophilic organocatalysts, based on phosphines, primary/secondary/tertiary amines, and N-heterocyclic carbenes, of either mono- or multifunctionality, derived from various chiral backbone scaffolds, have been rationally designed, meticulously optimized, and strategically applied for the preparation of such crucial molecular frameworks. In the following sections, enantioselective and diastereoselective (3 + 2) cycloaddition reactions catalyzed by chiral phosphines (P-nucleophiles), chiral amines (N-nucleophiles), and chiral N-heterocyclic carbenes (C-nucleophiles) reported over the past few decades are summarized and discussed in sequence." @default.
- W4313347103 created "2023-01-06" @default.
- W4313347103 creator A5000045799 @default.
- W4313347103 creator A5030174132 @default.
- W4313347103 creator A5030755202 @default.
- W4313347103 creator A5041992809 @default.
- W4313347103 creator A5042532928 @default.
- W4313347103 creator A5052134746 @default.
- W4313347103 date "2022-01-01" @default.
- W4313347103 modified "2023-09-27" @default.
- W4313347103 title "(3 + 2) Cycloadditions by Nucleophilic Organocatalysis" @default.
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