Strategic Use of Pinacol-Terminated Prins Cyclizations in Target-Oriented Total Synthesis
- 1 September 2003
- journal article
- review article
- Published by American Chemical Society (ACS) in The Journal of Organic Chemistry
- Vol. 68 (19), 7143-7157
- https://doi.org/10.1021/jo034982c
Abstract
No abstract availableKeywords
This publication has 40 references indexed in Scilit:
- Kinetic vs. Thermodynamic Control in Intramolecular Diene Cyclozirconation: Synthesis of Elemol.Tetrahedron Letters, 1995
- Stereocontrolled preparation of tetrahydrofurans from acid-promoted rearrangements of allylic acetals. [Erratum to document cited in CA115(13):135825m]Journal of the American Chemical Society, 1992
- Stereocontrolled preparation of tetrahydrofurans from acid-promoted rearrangements of allylic acetalsJournal of the American Chemical Society, 1991
- Retro-Diels-Alder cleavage of endo-bicyclo[2.2.1]hept-5-en-2-olThe Journal of Organic Chemistry, 1982
- Automerization of C11H11 chlorides and stability of their cationsJournal of the American Chemical Society, 1981
- Carbon-carbon bond formation via directed 2-azonia-[3,3]-sigmatropic rearrangements. A new pyrrolidine synthesisJournal of the American Chemical Society, 1979
- Structure and reactivity. 2. 2-tert-Butyl-3-cyano-7-oxabicyclo[4.1.0]heptane stereoisomers: pseudoaxial tert-butyl conformer and epoxidation reaction pathThe Journal of Organic Chemistry, 1978
- Photochemical reactions. LIX. Mechanism of the photodecarbonylation of .beta.,.gamma.-unsaturated aldehydesJournal of the American Chemical Society, 1970
- The Dissociation of Sterically Hindered AcidsJournal of the American Chemical Society, 1955
- Ueber künstliche Bildung des HarnstoffsAnnalen der Physik, 1828