From dioxime oxalates to dihydropyrroles and phenanthridines via iminyl radicals

Fernando Portela-Cubillo; Eoin M. Scanlan; Jackie S. Scott; John C. Walton

doi:10.1039/b808625g

From dioxime oxalates to dihydropyrroles and phenanthridines via iminyl radicals

Fernando Portela-Cubillo, Eoin M. Scanlan, Jackie S. Scott, John C. Walton

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

Abstract

Dioxime oxalates are useful precursors for the clean generation of iminyl radicals by sensitised UV photolysis and can be adapted for serviceable preparations of 3,4-dihydro-2H-pyrroles and phenanthridines.

Original language	English
Pages (from-to)	4189-4191
Number of pages	3
Journal	Chemical Communications
Issue number	35
DOIs	https://doi.org/10.1039/b808625g
Publication status	Published - 2008

Keywords

CYCLIZATIONS
OXIMES
O-2,4-DINITROPHENYLOXIMES
REARRANGEMENT

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title = "From dioxime oxalates to dihydropyrroles and phenanthridines via iminyl radicals",

abstract = "Dioxime oxalates are useful precursors for the clean generation of iminyl radicals by sensitised UV photolysis and can be adapted for serviceable preparations of 3,4-dihydro-2H-pyrroles and phenanthridines.",

keywords = "CYCLIZATIONS, OXIMES, O-2,4-DINITROPHENYLOXIMES, REARRANGEMENT",

author = "Fernando Portela-Cubillo and Scanlan, \{Eoin M.\} and Scott, \{Jackie S.\} and Walton, \{John C.\}",

year = "2008",

doi = "10.1039/b808625g",

language = "English",

pages = "4189--4191",

journal = "Chemical Communications",

issn = "1359-7345",

publisher = "Royal Society of Chemistry",

number = "35",

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T1 - From dioxime oxalates to dihydropyrroles and phenanthridines via iminyl radicals

AU - Portela-Cubillo, Fernando

AU - Scanlan, Eoin M.

AU - Scott, Jackie S.

AU - Walton, John C.

PY - 2008

Y1 - 2008

N2 - Dioxime oxalates are useful precursors for the clean generation of iminyl radicals by sensitised UV photolysis and can be adapted for serviceable preparations of 3,4-dihydro-2H-pyrroles and phenanthridines.

AB - Dioxime oxalates are useful precursors for the clean generation of iminyl radicals by sensitised UV photolysis and can be adapted for serviceable preparations of 3,4-dihydro-2H-pyrroles and phenanthridines.

KW - CYCLIZATIONS

KW - OXIMES

KW - O-2,4-DINITROPHENYLOXIMES

KW - REARRANGEMENT

UR - https://www.scopus.com/pages/publications/52049102418

U2 - 10.1039/b808625g

DO - 10.1039/b808625g

M3 - Article

SN - 1359-7345

SP - 4189

EP - 4191

JO - Chemical Communications

JF - Chemical Communications

IS - 35

ER -

From dioxime oxalates to dihydropyrroles and phenanthridines via iminyl radicals

Abstract

Keywords

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