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 journalArticlepeer-review

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

Bibliographical note

Funding Information:
This work was supported by a grant from the Korea Research Foundation (KRF-2003-015-C00360).

All Science Journal Classification (ASJC) codes

  • Biochemistry
  • Drug Discovery
  • Organic Chemistry

Fingerprint Dive into the research topics of 'Synthesis of cyclic hydrazines by ring-closing metathesis of dienes and enynes tethered by an N-N bond'. Together they form a unique fingerprint.

Cite this