Nucleophilic phosphine-catalyzed [3+2] cycloaddition of allenes with N-(thio)phosphoryl imines and acidic methanolysis of adducts N-(thio)phosphoryl 3-pyrrolines: a facile synthesis of free amine 3-pyrrolines
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference50 articles.
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4. Engaging Zwitterions in Carbon−Carbon and Carbon−Nitrogen Bond-Forming Reactions: A Promising Synthetic Strategy
5. For representative and recent examples, see:
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1. Phosphine-catalyzed [3 + 2] annulation of β-sulfonamido-substituted enones with trans-α-cyano-α,β-unsaturated ketones for the synthesis of highly substituted pyrrolidines;RSC Advances;2021
2. Phosphine‐Catalyzed (4+1) Annulation: Rearrangement of Allenylic Carbamates to 3‐Pyrrolines through Phosphonium Diene Intermediates;ChemCatChem;2020-07-30
3. Discussion Addendum for: Phosphine‐Catalyzed [3 + 2] Annulation: Synthesis of Ethyl 5‐( tert ‐Butyl)‐2‐Phenyl‐1‐Tosyl‐3‐Pyrroline‐3‐Carboxylate;Organic Syntheses;2020-04-29
4. Synthesis of heterocyclic compounds through nucleophilic phosphine catalysis;Chemical Communications;2020
5. Recent advances in phosphine catalysis involving γ-substituted allenoates;Chemical Communications;2020
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