Ring-Closing Metathesis of Enynes Tethered by an N-O Bond: Synthesis of 1,2-Oxaza Polycycles by Diels-Alder Reaction of the Ring-Closing Metathesis Products

Young Keun Yang, Jinsung Tae

Research output: Contribution to journalArticlepeer-review

44 Citations (Scopus)

Abstract

Ring-closing metathesis (RCM) reaction of enynes tethered by an N-O bond produced 6- to 8-membered 1,2-oxaza heterocyclic compounds in high yields. Diels-Alder reaction of the cyclic 1,3-dienes with various dienophiles afforded bi- or tri-cyclic compounds efficiently.

Original languageEnglish
Pages (from-to)2017-2020
Number of pages4
JournalSynlett
Issue number13
DOIs
Publication statusPublished - 2003

All Science Journal Classification (ASJC) codes

  • Organic Chemistry

Fingerprint

Dive into the research topics of 'Ring-Closing Metathesis of Enynes Tethered by an N-O Bond: Synthesis of 1,2-Oxaza Polycycles by Diels-Alder Reaction of the Ring-Closing Metathesis Products'. Together they form a unique fingerprint.

Cite this