A novel [3+2] dipolar cycloaddition approach to hexahydrobenzofuro [3,2-b] pyrroles

Ikyon Kim, Hee Kyung Na, Kyung Ran Kim, Sun Gi Kim, Ge Hyeong Lee

Research output: Contribution to journalArticle

13 Citations (Scopus)

Abstract

A highly stereoselective intramolecular 1,3-dipolar cycloaddition reaction of azomethine ylides derived from 2-vinyloxybenzaldehydes proceeded smoothly to allow for a direct access to tricyclic hexahydrobenzofuro[3,2-b]pyrroles in good yields.

Original languageEnglish
Pages (from-to)2069-2071
Number of pages3
JournalSynlett
Issue number13
DOIs
Publication statusPublished - 2008 Aug 1

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Pyrroles
Cycloaddition
azomethine

All Science Journal Classification (ASJC) codes

  • Organic Chemistry

Cite this

Kim, Ikyon ; Na, Hee Kyung ; Kim, Kyung Ran ; Kim, Sun Gi ; Lee, Ge Hyeong. / A novel [3+2] dipolar cycloaddition approach to hexahydrobenzofuro [3,2-b] pyrroles. In: Synlett. 2008 ; No. 13. pp. 2069-2071.
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A novel [3+2] dipolar cycloaddition approach to hexahydrobenzofuro [3,2-b] pyrroles. / Kim, Ikyon; Na, Hee Kyung; Kim, Kyung Ran; Kim, Sun Gi; Lee, Ge Hyeong.

In: Synlett, No. 13, 01.08.2008, p. 2069-2071.

Research output: Contribution to journalArticle

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