Strategies for the Formation of Tetrahydropyran Rings in the Synthesis of Natural Products
Top Cited Papers
- 13 April 2006
- journal article
- Published by Wiley in European Journal of Organic Chemistry
- Vol. 2006 (9) , 2045-2053
- https://doi.org/10.1002/ejoc.200500964
Abstract
No abstract availableKeywords
This publication has 59 references indexed in Scilit:
- Total Synthesis of (+)‐Dactylolide through an Efficient Sequential Peterson Olefination and Prins Cyclization ReactionAngewandte Chemie International Edition in English, 2005
- Total Synthesis of Apicularen A through Transannular Pyran FormationAngewandte Chemie International Edition in English, 2004
- Phorboxazole B synthetic studies: construction of C(1–32) and C(33–46) subtargetsOrganic & Biomolecular Chemistry, 2004
- Leucascandrolide A: Synthesis and Related StudiesThe Journal of Organic Chemistry, 2003
- Total synthesis of (+)-phorboxazole A, a potent cytostatic agent from the sponge Phorbas sp.Organic & Biomolecular Chemistry, 2003
- Total Synthesis of Natural (+)‐Lasonolide AAngewandte Chemie International Edition in English, 2003
- Macrolactonization via Ti(IV)-Mediated Epoxy-Acid Coupling: A Total Synthesis of (−)-Dactylolide [and Zampanolide]Journal of the American Chemical Society, 2003
- Total Synthesis of Phorboxazole AAngewandte Chemie International Edition in English, 2003
- Synthesis of the C(29)−C(45) Bis-pyran Subunit (E−F) of Spongistatin 1 (Altohyrtin A)The Journal of Organic Chemistry, 2000
- Stereocomplementary construction of 2-ethynyl-3-hydroxytetrahydrofuran derivatives via endo-mode ring closure of 3,4-epoxy-6-substitutedhex-5-yn-1-olsJournal of the Chemical Society, Chemical Communications, 1994