α-Methylen-β-lacton, ein neuer Heterocyclus durch Desoxygenierung von α-Methylen-β-peroxylactonen mit Triphenylphosphan
Author:
Publisher
Wiley
Subject
General Medicine
Reference8 articles.
1. in (Hrsg.): The Chemistry of Heterocyclic Compounds, Vol. 19, Part II, Wiley, New York 1964. S. 729–884.
2. On the mechanism of the triphenylphosphine-azodicarboxylate (Mitsunobu reaction) esterification
3. Synthese des ersten α-Methylen-β-peroxylactons – regiospezifische En-Reaktion von1O2 mit α,β-ungesättigten Carbonsäuren
4. Synthesis of the First ?-Methylene-?-peroxylactone?Regiospecific Ene Reaction of1O2 with ?,?-Unsaturated Carboxylic Acids
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1. Ligand‐Controlled Palladium‐Catalyzed Carbonylation of Alkynols: Highly Selective Synthesis of α‐Methylene‐β‐Lactones;Angewandte Chemie;2020-09-17
2. Ligand‐Controlled Palladium‐Catalyzed Carbonylation of Alkynols: Highly Selective Synthesis of α‐Methylene‐β‐Lactones;Angewandte Chemie International Edition;2020-09-17
3. Diels‐Alder Reaction of Racemic β1‐Isopropyl‐α1‐methylene‐β1‐lactone with Enantiomerically Pure 5,6,7,7a‐Tetrahydro‐7a‐methyl‐1‐phenyl‐4 H 1‐indene and Retro Cleavage of the Resulting Spiro‐β1‐lactones: The First Case of a Perfect Topological Resolution;Chemische Berichte;1993-06
4. Stereoselective Synthesis of α,β‐ trans 1‐Spiro‐β1‐lactones by Diels‐Alder Cycloaddition of 1,3‐Dienes to α1‐Methylene‐β1‐lactone and Their Decarboxylation by Pyrolysis to ( E )1‐Alkylidenecycloalkenes, a Convenient Olefination Method;Chemische Berichte;1993-06
5. α-Methylene-β-lactones as novel allene equivalents: regioselective [4+2] cycloaddition and stereoselective decarboxylation for the introduction of exo-alkylidene functionalities;Tetrahedron Letters;1991-11
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