Aryl iodide mediated aziridination of alkenes

Jiayin Li; Philip Wai Hong Chan; Chi Ming Che

doi:10.1021/ol052293c

Aryl iodide mediated aziridination of alkenes

Jiayin Li, Philip Wai Hong Chan, Chi Ming Che

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

63 Citations (Scopus)

Abstract

(Chemical Equation Presented) Aryl iodide mediated aziridination of a variety of alkenes with N-aminophthalimide under mild conditions (m-CPBA, K ₂CO₃, CH₂Cl₂, 25°C) was achieved in moderate to good yields (up to 94%). By recovering the aryl iodide, a recyclable system is developed with product yield over 79% attained for the aziridination of trans-1,2-diphenylethylene.

Original language	English
Pages (from-to)	5801-5804
Number of pages	4
Journal	Organic Letters
Volume	7
Issue number	26
DOIs	https://doi.org/10.1021/ol052293c
Publication status	Published - 22 Dec 2005
Externally published	Yes

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10.1021/ol052293c

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Cite this

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title = "Aryl iodide mediated aziridination of alkenes",

abstract = "(Chemical Equation Presented) Aryl iodide mediated aziridination of a variety of alkenes with N-aminophthalimide under mild conditions (m-CPBA, K 2CO3, CH2Cl2, 25°C) was achieved in moderate to good yields (up to 94%). By recovering the aryl iodide, a recyclable system is developed with product yield over 79% attained for the aziridination of trans-1,2-diphenylethylene.",

author = "Jiayin Li and Chan, {Philip Wai Hong} and Che, {Chi Ming}",

year = "2005",

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journal = "Organic Letters",

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AU - Chan, Philip Wai Hong

AU - Che, Chi Ming

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N2 - (Chemical Equation Presented) Aryl iodide mediated aziridination of a variety of alkenes with N-aminophthalimide under mild conditions (m-CPBA, K 2CO3, CH2Cl2, 25°C) was achieved in moderate to good yields (up to 94%). By recovering the aryl iodide, a recyclable system is developed with product yield over 79% attained for the aziridination of trans-1,2-diphenylethylene.

AB - (Chemical Equation Presented) Aryl iodide mediated aziridination of a variety of alkenes with N-aminophthalimide under mild conditions (m-CPBA, K 2CO3, CH2Cl2, 25°C) was achieved in moderate to good yields (up to 94%). By recovering the aryl iodide, a recyclable system is developed with product yield over 79% attained for the aziridination of trans-1,2-diphenylethylene.

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DO - 10.1021/ol052293c

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JF - Organic Letters

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