C1–C2 cleavage of C1-functionalized 8-oxabicyclo-[3.2.1]-oct-6-en-3-one. Stereoselective preparation of 4-substituted butenolides
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference54 articles.
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3. General method of assignment of relative stereochemistry in C-1-substituted 2,4-dimethyl-8-oxabicyclo[3.2.1]oct-6-en-3-one by1H and13C NMR correlations
4. alpha-Hetero-substituted Furans as Dienes in [4+3] Cycloadditions with 1,3-Dimethyloxyallyl Cation for the Preparation of New Versatile Cycloheptane Synthons: A Study of the Factors Controlling the Diastereoselectivity.
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