1,5‐Allyl Shift by a Sequential Achmatowicz/Oxonia‐Cope/Retro‐Achmatowicz Rearrangement
- 24 June 2022
- journal article
- Published by Wiley in Angewandte Chemie
- Vol. 134 (32)
- https://doi.org/10.1002/ange.202205919
Abstract
No abstract availableFunding Information
- Southern Marine Science and Engineering Guangdong Laboratory (SMSEGL20Sc01-B)
- University Grants Committee (C6026-19G, 16307219, 16304618, 16306920, 16300921)
This publication has 44 references indexed in Scilit:
- Die Prins-Makrocyclisierung als effiziente Ringschluss-Strategie in der NaturstoffsyntheseAngewandte Chemie, 2010
- Prins‐Type Macrocyclizations as an Efficient Ring‐Closing Strategy in Natural Product SynthesisAngewandte Chemie, 2010
- [3,3]-Sigmatropic rearrangements: recent applications in the total synthesis of natural productsChemical Society Reviews, 2009
- Solvolysis of a Tetrahydropyranyl Mesylate: Mechanistic Implications for the Prins Cyclization, 2-Oxonia-Cope Rearrangement, and Grob FragmentationOrganic Letters, 2006
- Utilization of an Oxonia-Cope Rearrangement as a Mechanistic Probe for Prins CyclizationsJournal of the American Chemical Society, 2005
- Julia–Colonna asymmetric epoxidation of furyl styryl ketone as a route to intermediates to naturally-occurring styryl lactonesJournal of the Chemical Society, Perkin Transactions 1, 1999
- [2,3]-Wittig sigmatropic rearrangements in organic synthesisChemical Reviews, 1986
- Conservation of orbital symmetryAccounts of Chemical Research, 1968
- The Chemistry of Eight-Membered Carbocycles.Chemical Reviews, 1951
- The Introduction of Substituted Vinyl Groups. V. A Rearrangement Involving the Migration of an Allyl Group in a Three-Carbon System1Journal of the American Chemical Society, 1940