Palladium‐Catalyzed Three‐Component Reaction of Enol Ethers, Salicylaldehyde, and Trimethyl Orthoformate: A Fast Synthesis of Tetrahydro‐<scp>2H</scp>,<scp>5H</scp>‐Pyrano[2,3‐b]Chromenes

ABSTRACT The Pd‐catalyzed three‐component reaction of enol ethers, methyl orthoformate, and salicylaldehyde is described. Both steroid and non‐steroid enol ethers are compatible. This reaction allows the construction of tetrahydro‐2H,5H‐pyrano[2,3‐b]chromene. Unambiguous NMR characterization and X‐ray diffraction structures are provided.

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Publication Details

Journal
Journal of Heterocyclic Chemistry
Published
2025-03-02
DOI
https://doi.org/10.1002/jhet.4949
Citations
1
Primary Topic
Synthesis of Organic Compounds
Type
article
Field-Weighted Citation Impact
1.39
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article

Palladium‐Catalyzed Three‐Component Reaction of Enol Ethers, Salicylaldehyde, and Trimethyl Orthoformate: A Fast Synthesis of Tetrahydro‐2H,5H‐Pyrano[2,3‐b]Chromenes

Martín A. Iglesias‐Arteaga, Marcos Flores-Álamo, William H. García‐Santos, José A. Olivares‐Castillo et al.
1 citations
Journal of Heterocyclic Chemistry
Synthesis of Organic Compounds
1.39
article

Palladium‐Catalyzed Three‐Component Reaction of Enol Ethers, Salicylaldehyde, and Trimethyl Orthoformate: A Fast Synthesis of Tetrahydro‐2H,5H‐Pyrano[2,3‐b]Chromenes

Martín A. Iglesias‐Arteaga, Marcos Flores-Álamo, William H. García‐Santos, José A. Olivares‐Castillo, Melina D. Cordova‐Rodríguez
article en
1 citations

Abstract

ABSTRACT The Pd‐catalyzed three‐component reaction of enol ethers, methyl orthoformate, and salicylaldehyde is described. Both steroid and non‐steroid enol ethers are compatible. This reaction allows the construction of tetrahydro‐2H,5H‐pyrano[2,3‐b]chromene. Unambiguous NMR characterization and X‐ray diffraction structures are provided.

Journal of Heterocyclic ChemistryVol. 62(5-6)
Universidad Autónoma de la Ciudad de México (MX), Universidad Nacional Autónoma de México (MX)
Openalex Percentile: Top 23%
Synthesis of Organic Compounds
1.39
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