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

74 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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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",

month = dec,

day = "22",

doi = "10.1021/ol052293c",

language = "English",

volume = "7",

pages = "5801--5804",

journal = "Organic Letters",

issn = "1523-7060",

publisher = "American Chemical Society",

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T1 - Aryl iodide mediated aziridination of alkenes

AU - Li, Jiayin

AU - Chan, Philip Wai Hong

AU - Che, Chi Ming

PY - 2005/12/22

Y1 - 2005/12/22

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.

UR - https://www.scopus.com/pages/publications/30144446386

U2 - 10.1021/ol052293c

DO - 10.1021/ol052293c

M3 - Article

AN - SCOPUS:30144446386

SN - 1523-7060

VL - 7

SP - 5801

EP - 5804

JO - Organic Letters

JF - Organic Letters

IS - 26

ER -

Aryl iodide mediated aziridination of alkenes

Abstract

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