Debenzylative Cycloetherification: An Overlooked Key Strategy for Complex Tetrahydrofuran Synthesis |
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Authors: | Dr. Abdellatif Tikad Julien A. Delbrouck Prof. Stéphane P. Vincent |
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Affiliation: | University of Namur (UNamur), Département de Chimie, Laboratoire de Chimie Bio-Organique, Namur, Belgium |
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Abstract: | Tetrahydrofuran (THF) is a major structural feature found in many synthetic and natural products displaying a variety of biological properties. This review summarizes the main synthetic approaches that have been developed to construct tetrahydrofuran moieties involving debenzylative cycloetherification reactions (DBCE). Interestingly, this reaction is regio‐ and stereoselective without the requirement of a selective protection/deprotection strategy. Many applications of this process have been reported, including carbafuranoside synthesis, regioselective deprotection of the benzyl group positioned γ to an alkene, and total synthesis of natural products. The stereochemical outcome and the mechanism of these interesting transformations are also discussed. |
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Keywords: | heterocycles cyclization stereoselectivity tetrahydrofuran total synthesis |
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