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

Jinsung Tae; Dong Woo Hahn

doi:10.1016/j.tetlet.2004.03.075

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

Jinsung Tae, Dong Woo Hahn

Department of Chemistry

Research output: Contribution to journal › Article › peer-review

22 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 language	English
Pages (from-to)	3757-3760
Number of pages	4
Journal	Tetrahedron Letters
Volume	45
Issue number	19
DOIs	https://doi.org/10.1016/j.tetlet.2004.03.075
Publication status	Published - 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

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10.1016/j.tetlet.2004.03.075

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

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.",

author = "Jinsung Tae and Hahn, {Dong Woo}",

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

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AU - Tae, Jinsung

AU - Hahn, Dong Woo

N1 - Funding Information: This work was supported by a grant from the Korea Research Foundation (KRF-2003-015-C00360).

PY - 2004/5/3

Y1 - 2004/5/3

N2 - 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.

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

Abstract

Bibliographical note

All Science Journal Classification (ASJC) codes

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