Synthesis of a 2,3′;6′,3″-terpyridine scaffold as an α-helix mimetic

Jessica M. Davis; Anh Truong; Andrew D. Hamilton

doi:10.1021/ol0521228

Synthesis of a 2,3′;6′,3″-terpyridine scaffold as an α-helix mimetic

Jessica M. Davis, Anh Truong, Andrew D. Hamilton

Chemistry

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

Abstract

(Chemical Equation Presented) A terpyridine scaffold has been designed as an α-helix mimetic. A facile synthesis of the ortho-functionalized 2,3′-oligopyridine has been accomplished using sequential Bohlmann-Rahtz heteroannulation reactions.

Original language	English (US)
Pages (from-to)	5405-5408
Number of pages	4
Journal	Organic Letters
Volume	7
Issue number	24
DOIs	https://doi.org/10.1021/ol0521228
State	Published - Nov 24 2005

ASJC Scopus subject areas

Biochemistry
Physical and Theoretical Chemistry
Organic Chemistry

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10.1021/ol0521228

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title = "Synthesis of a 2,3′;6′,3″-terpyridine scaffold as an α-helix mimetic",

abstract = "(Chemical Equation Presented) A terpyridine scaffold has been designed as an α-helix mimetic. A facile synthesis of the ortho-functionalized 2,3′-oligopyridine has been accomplished using sequential Bohlmann-Rahtz heteroannulation reactions.",

author = "Davis, {Jessica M.} and Anh Truong and Hamilton, {Andrew D.}",

year = "2005",

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AU - Davis, Jessica M.

AU - Truong, Anh

AU - Hamilton, Andrew D.

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N2 - (Chemical Equation Presented) A terpyridine scaffold has been designed as an α-helix mimetic. A facile synthesis of the ortho-functionalized 2,3′-oligopyridine has been accomplished using sequential Bohlmann-Rahtz heteroannulation reactions.

AB - (Chemical Equation Presented) A terpyridine scaffold has been designed as an α-helix mimetic. A facile synthesis of the ortho-functionalized 2,3′-oligopyridine has been accomplished using sequential Bohlmann-Rahtz heteroannulation reactions.

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JO - Organic Letters

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Synthesis of a 2,3′;6′,3″-terpyridine scaffold as an α-helix mimetic

Abstract

ASJC Scopus subject areas

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