An efficient strategy for the iterative synthesis of a trans-fused polytetrahydropyran ring system via SmI2-induced reductive intramolecular cyclization
- 1 April 1999
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 40 (14) , 2811-2814
- https://doi.org/10.1016/s0040-4039(99)00301-9
Abstract
No abstract availableKeywords
This publication has 39 references indexed in Scilit:
- Diastereoselective Synthesis of Cyclic Ethers by Radical Cyclization at β-Position of β-AlkoxyacrylatesSynthetic Communications, 1997
- A New Strategy for the Reiterative Synthesis of trans-Fused Tetrahydropyrans via Alkylation of Oxiranyl Anion and 6-endo CyclizationJournal of the American Chemical Society, 1996
- Stereoselective Construction of Cyclic Ethers via Intramolecular Acyl Radical Cyclizations: A Practical Solution to DecarbonylationThe Journal of Organic Chemistry, 1996
- An Iterative Approach to Biologically Important Fused Polycyclic Ethers via Acyl Radical CyclizationsThe Journal of Organic Chemistry, 1996
- Samarium(II) Iodide Promoted Intermolecular Ketone-Olefin Couplings Chelation-Controlled by .alpha.-Hydroxyl GroupsThe Journal of Organic Chemistry, 1994
- Stereocontrolled synthesis of the hemibrevetoxin ring system via an allylic tin methodJournal of the Chemical Society, Chemical Communications, 1993
- Application of lanthanide reagents in organic synthesisChemical Reviews, 1992
- Synthesis of the brevetoxin B IJK ring systemJournal of the American Chemical Society, 1989
- Methods for pyranoannulation: an approach to a new class of polyethersThe Journal of Organic Chemistry, 1985
- Alternative synthesis of (±)-eburunamenine via cleavage of a cyclic dithioacetal of an α-oxo-thioneJournal of the Chemical Society, Chemical Communications, 1977