Iodination of aryl amines in a water-paste form via stable aryl diazonium tosylates

Dmitry A. Gorlushko, Victor D. Filimonov, Elena A. Krasnokutskaya, Nadya I. Semenischeva, Bong Seong Go, Ho Yun Hwang, Eun Hye Cha, Ki Whan Chi

Результат исследований: Материалы для журналаСтатья

50 Цитирования (Scopus)

Выдержка

The diazotization of aryl amines at room temperature in paste form with NaNO2, p-TsOH and a small amount of water, followed by treatment with KI provides a new, simple, and effective route for the preparation of various aryl iodides. The water-paste and strong acid-free reaction conditions are environmentally friendly and compatible with acid-sensitive functional groups.

Язык оригиналаАнглийский
Страницы (с-по)1080-1082
Число страниц3
ЖурналTetrahedron Letters
Том49
Номер выпуска6
DOI
СостояниеОпубликовано - 4 фев 2008

Отпечаток

Halogenation
Ointments
Amines
Acids
Water
Water Purification
Iodides
Functional groups
Temperature

ASJC Scopus subject areas

  • Biochemistry
  • Organic Chemistry
  • Drug Discovery

Цитировать

Iodination of aryl amines in a water-paste form via stable aryl diazonium tosylates. / Gorlushko, Dmitry A.; Filimonov, Victor D.; Krasnokutskaya, Elena A.; Semenischeva, Nadya I.; Go, Bong Seong; Hwang, Ho Yun; Cha, Eun Hye; Chi, Ki Whan.

В: Tetrahedron Letters, Том 49, № 6, 04.02.2008, стр. 1080-1082.

Результат исследований: Материалы для журналаСтатья

Gorlushko, Dmitry A. ; Filimonov, Victor D. ; Krasnokutskaya, Elena A. ; Semenischeva, Nadya I. ; Go, Bong Seong ; Hwang, Ho Yun ; Cha, Eun Hye ; Chi, Ki Whan. / Iodination of aryl amines in a water-paste form via stable aryl diazonium tosylates. В: Tetrahedron Letters. 2008 ; Том 49, № 6. стр. 1080-1082.
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AU - Filimonov, Victor D.

AU - Krasnokutskaya, Elena A.

AU - Semenischeva, Nadya I.

AU - Go, Bong Seong

AU - Hwang, Ho Yun

AU - Cha, Eun Hye

AU - Chi, Ki Whan

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AB - The diazotization of aryl amines at room temperature in paste form with NaNO2, p-TsOH and a small amount of water, followed by treatment with KI provides a new, simple, and effective route for the preparation of various aryl iodides. The water-paste and strong acid-free reaction conditions are environmentally friendly and compatible with acid-sensitive functional groups.

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