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

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

Research output: Contribution to journalArticlepeer-review

55 Citations (Scopus)

Abstract

A facile two-step synthesis of a series of benzo-fused 2,8-dioxabicyclo[3.3.1]nonane derivatives is described, featuring a domino Knoevenagel condensation/intramolecular hetero-Diels-Alder reaction sequence.

Original languageEnglish
Pages (from-to)664-671
Number of pages8
JournalTetrahedron
Volume64
Issue number4
DOIs
Publication statusPublished - 2008 Jan 21

Bibliographical note

Funding Information:
We thank the Center for Biological Modulators and Korea Research Institute of Chemical Technology for generous financial support.

All Science Journal Classification (ASJC) codes

  • Biochemistry
  • Drug Discovery
  • Organic Chemistry

Fingerprint Dive into the research topics of 'Facile synthesis of benzo-fused 2,8-dioxabicyclo[3.3.1]nonane derivatives via a domino Knoevenagel condensation/hetero-Diels-Alder reaction sequence'. Together they form a unique fingerprint.

Cite this