1,6-C-H insertion of alkylidenecarbenes in 1-naphthol and 1-anthrol derivatives

Ken S. Feldman; Angela L. Perkins

doi:10.1016/S0040-4039(01)01208-4

1,6-C-H insertion of alkylidenecarbenes in 1-naphthol and 1-anthrol derivatives

Ken S. Feldman, Angela L. Perkins

Chemistry

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44 Scopus citations

Abstract

Rare 1,6-C-H insertion of naphthol- and anthrol-derived alkylidenecarbenes has been observed in modest yield. Reaction in deuterated solvent did not provide any evidence in support of a reaction mechanism that requires exchange of the migrating proton with solvent. The pyran-annelated aromatic products are formed only when opportunities for the more common 1,5-C-H insertion process are blocked.

Original language	English (US)
Pages (from-to)	6031-6033
Number of pages	3
Journal	Tetrahedron Letters
Volume	42
Issue number	35
DOIs	https://doi.org/10.1016/S0040-4039(01)01208-4
State	Published - Aug 27 2001

All Science Journal Classification (ASJC) codes

Biochemistry
Drug Discovery
Organic Chemistry

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10.1016/S0040-4039(01)01208-4

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title = "1,6-C-H insertion of alkylidenecarbenes in 1-naphthol and 1-anthrol derivatives",

abstract = "Rare 1,6-C-H insertion of naphthol- and anthrol-derived alkylidenecarbenes has been observed in modest yield. Reaction in deuterated solvent did not provide any evidence in support of a reaction mechanism that requires exchange of the migrating proton with solvent. The pyran-annelated aromatic products are formed only when opportunities for the more common 1,5-C-H insertion process are blocked.",

author = "Feldman, {Ken S.} and Perkins, {Angela L.}",

note = "Funding Information: We thank the National Institutes of Health (GM37681) for financial support of this work.",

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T1 - 1,6-C-H insertion of alkylidenecarbenes in 1-naphthol and 1-anthrol derivatives

AU - Feldman, Ken S.

AU - Perkins, Angela L.

N1 - Funding Information: We thank the National Institutes of Health (GM37681) for financial support of this work.

PY - 2001/8/27

Y1 - 2001/8/27

N2 - Rare 1,6-C-H insertion of naphthol- and anthrol-derived alkylidenecarbenes has been observed in modest yield. Reaction in deuterated solvent did not provide any evidence in support of a reaction mechanism that requires exchange of the migrating proton with solvent. The pyran-annelated aromatic products are formed only when opportunities for the more common 1,5-C-H insertion process are blocked.

AB - Rare 1,6-C-H insertion of naphthol- and anthrol-derived alkylidenecarbenes has been observed in modest yield. Reaction in deuterated solvent did not provide any evidence in support of a reaction mechanism that requires exchange of the migrating proton with solvent. The pyran-annelated aromatic products are formed only when opportunities for the more common 1,5-C-H insertion process are blocked.

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U2 - 10.1016/S0040-4039(01)01208-4

DO - 10.1016/S0040-4039(01)01208-4

M3 - Article

AN - SCOPUS:0035959487

SN - 0040-4039

VL - 42

SP - 6031

EP - 6033

JO - Tetrahedron Letters

JF - Tetrahedron Letters

IS - 35

ER -

1,6-C-H insertion of alkylidenecarbenes in 1-naphthol and 1-anthrol derivatives

Abstract

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