Convenient synthesis of 9-alkyl and 9-arylacridines from [2 - (trimethylsilyl) ethoxy] methyl (sem) protected acridone

Zijian Zeng; Steven C. Zimmerman

doi:10.1016/S0040-4039(00)80696-6

Convenient synthesis of 9-alkyl and 9-arylacridines from [2 - (trimethylsilyl) ethoxy] methyl (sem) protected acridone

Zijian Zeng, Steven C. Zimmerman

Chemistry

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

Abstract

The low yielding addition of organolithium reagents to acridone becomes a convenient high yielding route to 9-alkyl and 9-arylacridines when SEM-acridone is used.

Original language	English (US)
Pages (from-to)	5123-5124
Number of pages	2
Journal	Tetrahedron Letters
Volume	29
Issue number	40
DOIs	https://doi.org/10.1016/S0040-4039(00)80696-6
State	Published - 1988

ASJC Scopus subject areas

Biochemistry
Drug Discovery
Organic Chemistry

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10.1016/S0040-4039(00)80696-6

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title = "Convenient synthesis of 9-alkyl and 9-arylacridines from [2 - (trimethylsilyl) ethoxy] methyl (sem) protected acridone",

abstract = "The low yielding addition of organolithium reagents to acridone becomes a convenient high yielding route to 9-alkyl and 9-arylacridines when SEM-acridone is used.",

author = "Zijian Zeng and {C. Zimmerman}, Steven",

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AU - C. Zimmerman, Steven

PY - 1988

Y1 - 1988

N2 - The low yielding addition of organolithium reagents to acridone becomes a convenient high yielding route to 9-alkyl and 9-arylacridines when SEM-acridone is used.

AB - The low yielding addition of organolithium reagents to acridone becomes a convenient high yielding route to 9-alkyl and 9-arylacridines when SEM-acridone is used.

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DO - 10.1016/S0040-4039(00)80696-6

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JO - Tetrahedron Letters

JF - Tetrahedron Letters

IS - 40

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Convenient synthesis of 9-alkyl and 9-arylacridines from [2 - (trimethylsilyl) ethoxy] methyl (sem) protected acridone

Abstract

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