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- W2970577425 endingPage "9330" @default.
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- W2970577425 abstract "Abstract 2‐(Hetero)arylpyrrolidine fragment is found in a diverse array of biologically active molecules, both natural and unnatural. In recent years, a substantial increase in number of approved drugs featuring this scaffold is observed. Developing methods for the synthesis of such compounds has been essential for making progress in this field. Most of these methods require usage of metal catalysts and introduce additional chemical steps to obtain appropriately substituted starting compounds. This microreview details the one‐pot approach for the synthesis of pyrrolidine derivatives possessing (hetero)aromatic substituent at the second position of pyrrolidine ring based on usage of readily available N ‐substituted 4,4‐diethoxybutan‐1‐amines and (hetero)aromatics as starting compounds and Bronsted acids as catalysts." @default.
- W2970577425 created "2019-09-05" @default.
- W2970577425 creator A5010715704 @default.
- W2970577425 creator A5020754467 @default.
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- W2970577425 creator A5056118533 @default.
- W2970577425 creator A5060085599 @default.
- W2970577425 creator A5063237967 @default.
- W2970577425 date "2019-08-26" @default.
- W2970577425 modified "2023-09-26" @default.
- W2970577425 title "Acid‐Catalyzed Cascade Reaction of 4‐Aminobutanal Derivatives with (Hetero)aromatic Nucleophiles: A Versatile One‐Pot Access to 2‐(Hetero)arylpyrrolidines." @default.
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- W2970577425 doi "https://doi.org/10.1002/slct.201902011" @default.
- W2970577425 hasPublicationYear "2019" @default.
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