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
Author:
Publisher
The Chemical Society of Japan
Subject
General Chemistry
Link
https://www.jstage.jst.go.jp/article/cl/25/12/25_12_1035/_pdf
Reference12 articles.
1. Stereocontrolled Construction of Complex Cyclic Ketones via Oxy-Cope Rearrangement
2. Synthetic equivalents of the taxol C,D ring system. Examination of nucleophilic bicyclic oxetanes and less-strained acetonide equivalents
3. A means for stereocontrolled introduction of the C-2 oxygen substituent in functionalized cis-tricyclo[9.3.1.03,8]pentadecanones related to taxol
4. Tandem Cope-Cope Rearrangements
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1. An efficient total synthesis of (±)-ar-tenuifolene;Tetrahedron Letters;2015-09
2. N[1,3]-sigmatropic shift in the benzidine rearrangement: experimental and theoretical investigation;Org. Biomol. Chem.;2014
3. Mechanistic Insight into the Formal [1,3]-Migration in the Thermal Claisen Rearrangement;The Journal of Organic Chemistry;2012-11-20
4. ChemInform Abstract: 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.;ChemInform;2010-08-04
5. One or More CH, CC, and/or CC Bond(s) Formed by Rearrangement;Comprehensive Organic Functional Group Transformations II;2005
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