Synthesis of cyclic hydrazines by ring-closing metathesis of dienes and enynes tethered by an N-N bond

Jinsung Tae, Dong Woo Hahn

Research output: Contribution to journalArticle

20 Citations (Scopus)

Abstract

Ring-closing metathesis of dienes and enynes tethered by an N-N bond produced 6- to 10-membered cyclic 1,2-diaza compounds. The enyne RCM adducts were further transformed by Diels-Alder reaction into aromatic compounds.

Original languageEnglish
Pages (from-to)3757-3760
Number of pages4
JournalTetrahedron Letters
Volume45
Issue number19
DOIs
Publication statusPublished - 2004 May 3

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Hydrazines
Aromatic compounds
Cycloaddition Reaction

All Science Journal Classification (ASJC) codes

  • Biochemistry
  • Drug Discovery
  • Organic Chemistry

Cite this

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abstract = "Ring-closing metathesis of dienes and enynes tethered by an N-N bond produced 6- to 10-membered cyclic 1,2-diaza compounds. The enyne RCM adducts were further transformed by Diels-Alder reaction into aromatic compounds.",
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Synthesis of cyclic hydrazines by ring-closing metathesis of dienes and enynes tethered by an N-N bond. / Tae, Jinsung; Hahn, Dong Woo.

In: Tetrahedron Letters, Vol. 45, No. 19, 03.05.2004, p. 3757-3760.

Research output: Contribution to journalArticle

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AU - Hahn, Dong Woo

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AB - Ring-closing metathesis of dienes and enynes tethered by an N-N bond produced 6- to 10-membered cyclic 1,2-diaza compounds. The enyne RCM adducts were further transformed by Diels-Alder reaction into aromatic compounds.

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