Hypervalent iodine in synthesis 64: Syntheses of diaryl selenides and alkyl aryl selenides by palladium-catalyzed arylation of areneselenyl or alkaneselenyl magnesium bromide with diaryliodonium salt

Li Wang; Zhen-Chu Chen; Qin-Guo Zheng

doi:10.1002/cjoc.20020201152

Hypervalent iodine in synthesis 64: Syntheses of diaryl selenides and alkyl aryl selenides by palladium-catalyzed arylation of areneselenyl or alkaneselenyl magnesium bromide with diaryliodonium salt

Li Wang, Zhen-Chu Chen, Qin-Guo Zheng

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

Abstract

Areneselenyl or alkaneselenyl magnesium bromide reacts rapidly with diaryliodonium salt to give the corresponding diaryl or alkyl aryl selenide in the presence of catalytic amounts of Pd-(PPh₃)₄ in good yield.

Original language	English
Pages (from-to)	1457-1459
Number of pages	3
Journal	Chinese Journal of Chemistry
Volume	20
Issue number	11
DOIs	https://doi.org/10.1002/cjoc.20020201152
Publication status	Published - Nov 2002

Keywords

diaryliodonium salt
arylation
palladium catalyst
selenide

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10.1002/cjoc.20020201152

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title = "Hypervalent iodine in synthesis 64: Syntheses of diaryl selenides and alkyl aryl selenides by palladium-catalyzed arylation of areneselenyl or alkaneselenyl magnesium bromide with diaryliodonium salt",

abstract = "Areneselenyl or alkaneselenyl magnesium bromide reacts rapidly with diaryliodonium salt to give the corresponding diaryl or alkyl aryl selenide in the presence of catalytic amounts of Pd-(PPh3)4 in good yield.",

keywords = "diaryliodonium salt, arylation, palladium catalyst, selenide",

author = "Li Wang and Zhen-Chu Chen and Qin-Guo Zheng",

year = "2002",

month = nov,

doi = "10.1002/cjoc.20020201152",

language = "English",

volume = "20",

pages = "1457--1459",

journal = "Chinese Journal of Chemistry",

issn = "1001-604X",

publisher = "Shanghai Institute of Organic Chemistry",

number = "11",

}

Hypervalent iodine in synthesis 64: Syntheses of diaryl selenides and alkyl aryl selenides by palladium-catalyzed arylation of areneselenyl or alkaneselenyl magnesium bromide with diaryliodonium salt. / Wang, Li; Chen, Zhen-Chu; Zheng, Qin-Guo.
In: Chinese Journal of Chemistry, Vol. 20, No. 11, 11.2002, p. 1457-1459.

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

TY - JOUR

T1 - Hypervalent iodine in synthesis 64

T2 - Syntheses of diaryl selenides and alkyl aryl selenides by palladium-catalyzed arylation of areneselenyl or alkaneselenyl magnesium bromide with diaryliodonium salt

AU - Wang, Li

AU - Chen, Zhen-Chu

AU - Zheng, Qin-Guo

PY - 2002/11

Y1 - 2002/11

N2 - Areneselenyl or alkaneselenyl magnesium bromide reacts rapidly with diaryliodonium salt to give the corresponding diaryl or alkyl aryl selenide in the presence of catalytic amounts of Pd-(PPh3)4 in good yield.

AB - Areneselenyl or alkaneselenyl magnesium bromide reacts rapidly with diaryliodonium salt to give the corresponding diaryl or alkyl aryl selenide in the presence of catalytic amounts of Pd-(PPh3)4 in good yield.

KW - diaryliodonium salt

KW - arylation

KW - palladium catalyst

KW - selenide

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UR - http://onlinelibrary.wiley.com/doi/10.1002/cjoc.20020201152/abstract

U2 - 10.1002/cjoc.20020201152

DO - 10.1002/cjoc.20020201152

M3 - Article

SN - 1001-604X

VL - 20

SP - 1457

EP - 1459

JO - Chinese Journal of Chemistry

JF - Chinese Journal of Chemistry

IS - 11

ER -

Hypervalent iodine in synthesis 64: Syntheses of diaryl selenides and alkyl aryl selenides by palladium-catalyzed arylation of areneselenyl or alkaneselenyl magnesium bromide with diaryliodonium salt

Abstract

Keywords

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