Construction of Azaspirocyclic Ketones through α-Hydroxyiminium Ion or α-Siloxy Epoxide Semipinacol Rearrangements
- 1 June 2001
- journal article
- research article
- Published by American Chemical Society (ACS) in Organic Letters
- Vol. 3 (13) , 2109-2112
- https://doi.org/10.1021/ol0160708
Abstract
No abstract availableKeywords
This publication has 13 references indexed in Scilit:
- 1-Oxaspiro[4.4]nonan-6-ones. Synthetic Access via Oxonium Ion Technology, Optical Resolution, and Conversion into Enantiopure Spirocyclic α,β-ButenolidesThe Journal of Organic Chemistry, 2001
- A Solution to the Cyclic Aldol ProblemOrganic Letters, 2000
- Stereocontrolled synthesis of spirocyclicsTetrahedron, 1999
- Synthesis of (−)-Histrionicotoxin by a Tandem ProcessJournal of the American Chemical Society, 1999
- Synthesis and Further Reactivity of Functionalized Lactam-Derived Enol TriflatesThe Journal of Organic Chemistry, 1997
- Practical Synthesis of Spirocyclic Bis-C,C-glycosides. Mechanistic Models in Explanation of Rearrangement Stereoselectivity and the Bifurcation of Reaction PathwaysThe Journal of Organic Chemistry, 1997
- Single Stereodifferentiation Associated with Carbon Atom Insertion during the Oxonium Ion-Initiated Pinacol Rearrangement of Dihydrofuranyl and Dihydropyranyl CarbinolsThe Journal of Organic Chemistry, 1997
- Vinylcyclobutanols: A Composite Functional Group?Journal of the American Chemical Society, 1996
- First total synthesis of Lycopodium alkaloids of the magellanane group. Enantioselective total syntheses of (-)-magellanine and (+)-magellaninoneJournal of the American Chemical Society, 1993
- Epoxy silyl ether rearrangements: a new, stereoselective approach to the synthesis of .beta.-hydroxy carbonyl compoundsJournal of the American Chemical Society, 1986