Facile synthesis of benzo-fused 2,8-dioxabicyclo[3.3.1]nonane derivatives via a domino Knoevenagel condensation/hetero-Diels-Alder reaction sequence

Tetrahedron

Volumn 64, Issue 4, 2008, Pages 664-671

  Kim, Ikyon ^a   Kim, Sun Gi ^a   Choi, Jihyun ^a   Lee, Ge Hyeong ^a  

^a Korea Research Institute of Chemical Technology   (South Korea)

Author keywords

Benzo fused 2,8 dioxabicyclo 3.3.1 nonanes; Domino reaction; Hetero Diels Aldercycloaddition; Knoevenagel condensation; Proline

Indexed keywords

2,8 DIOXABICYCLO[3.3.1]NONANE DERIVATIVE; NONANE; PROLINE; UNCLASSIFIED DRUG;

ARTICLE; CHEMICAL STRUCTURE; CRYSTAL STRUCTURE; CYCLOADDITION; DIELS ALDER REACTION; KNOEVENAGEL CONDENSATION; MICHAEL ADDITION; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; PRIORITY JOURNAL; REACTION ANALYSIS; SYNTHESIS; X RAY CRYSTALLOGRAPHY;

ALNUS;

EID: 36849023139     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2007.11.036     Document Type: Article

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