Carbanion-induced intramolecular beta-cleavage reactions of 2-oxetanones
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference10 articles.
1. Intramolecular Ring Opening of Epoxides by Bis-Activated Carbanions. The Influence of Ring Size on Reactivity and Selectivity
2. TRANSFORMATION OF β-ALKENYL-β-PROPIOLACTONES INTO CYCLOPROPYLACETIC ACIDS UTILIZING HYDROBORATION
3. Conversion of serine to stereochemically pure .beta.-substituted .alpha.-amino acids via .beta.-lactones
4. Carbonyl assisted intramolecular ring opening of 2-oxetanones: A stereoselective route to 2,5-disubstituted tetrahydrofurans
5. Intramolecular ring-opening reactions of 2-oxetanones leading to tetrahydrofuran ring formation: a Lewis-acid study
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5. Studies of the tandem Mukaiyama aldol-lactonization (TMAL) reaction: A concise and highly diastereoselective route to β-lactones applied to the total synthesis of the potent pancreatic lipase inhibitor, (−)-Panclicin D;Tetrahedron;1997-12
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