UYEHARA Tadao | Department of Applied Chemistry, Faculty of Engineering, Utsunomiya University

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Rearrangement Approaches to Cyclic Skeletons. X. Pinacol-Type Rearrangement of 2-Substituted 1-Methoxybicyclo[2.2.2]oct-5-en-2-ols into Bicyclo[3.2.1]oct-6-en-2-ones. Remarkable Substituent Effects on Predominant Migration of the Unsaturated Bridge^
Rearrangement Approaches to Cyclic Skeletons. XIII.^ Total Synthesis of Triquinane Sesquiterpenes, (±)-Modhephene, and (±)-Isocomene, on the Basis of Formal Substitution at Both Bridgeheads of a Bicyclo[2.2.2]oct-5-en-2-one^
Rearrangement Approaches to Cyclic Skeletons. XI. Chemoenzymatic Preparation of Chiral Bridged Compounds for Rearrangement Approaches^
Diquinane Synthesis Based on Anionic[1, 3]Sigmatropic Rearrangements of an Oxy-Cope System Incorporated in the Bicyclo[3. 2. 1]oct-6-ene Framework
Anionic [1, 3] Sigmatropic Rearrangements of an Oxy-Cope System Incorporated in 8-Methylenebicyclo [3. 2. 1] oct-6-ene and Related Frameworks
Rearrangement Approaches to Cyclic Skeletons. IX. Stereoselective Total Synthesis of (±)-Camphorenone Based Reliable One-Step Diazo Transfer Followed by a Wolff Rearrangement
Lewis Acid-Promoted [2+2] Azetidine Annulation of N-A cylaldimines with Allyltriisopropylsilane
Rearrangement Approaches to Cyclic Skeletons. XII. Acid-Catalyzed Isomerization of Bicyclo[3. 2. 1]oct-6-en-2-ones into Bicyclo[3. 2. 1]oct-3-en-2-ones without Racemization^

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