One-pot preparation of arylalkynes by a tandem catalytic iodination of arenes and palladium-catalyzed coupling of iodoarenes with terminal alkynes

Shun Wan; Sunewang R. Wang; Wenjun Lu

doi:10.1021/jo060424x

One-pot preparation of arylalkynes by a tandem catalytic iodination of arenes and palladium-catalyzed coupling of iodoarenes with terminal alkynes

Shun Wan, Sunewang R. Wang, Wenjun Lu

Shanghai Jiao Tong University

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

53 Scopus citations

Abstract

Iodination of activated arenes by air-oxidation is carried out in the presence of catalytic bismuth salts at room temperature. Subsequently, the formed iodoarenes react with terminal alkynes to give arylalkynes under a selected palladium-catalyzed coupling condition in the same pot.

Original language	English
Pages (from-to)	4349-4352
Number of pages	4
Journal	Journal of Organic Chemistry
Volume	71
Issue number	11
DOIs	https://doi.org/10.1021/jo060424x
State	Published - 26 May 2006
Externally published	Yes

Access to Document

10.1021/jo060424x

Cite this

@article{32b09d645e1f4e0f919f88eb97f951ce,

title = "One-pot preparation of arylalkynes by a tandem catalytic iodination of arenes and palladium-catalyzed coupling of iodoarenes with terminal alkynes",

abstract = "Iodination of activated arenes by air-oxidation is carried out in the presence of catalytic bismuth salts at room temperature. Subsequently, the formed iodoarenes react with terminal alkynes to give arylalkynes under a selected palladium-catalyzed coupling condition in the same pot.",

author = "Shun Wan and Wang, \{Sunewang R.\} and Wenjun Lu",

year = "2006",

month = may,

day = "26",

doi = "10.1021/jo060424x",

language = "英语",

volume = "71",

pages = "4349--4352",

journal = "Journal of Organic Chemistry",

issn = "0022-3263",

publisher = "American Chemical Society",

number = "11",

}

TY - JOUR

T1 - One-pot preparation of arylalkynes by a tandem catalytic iodination of arenes and palladium-catalyzed coupling of iodoarenes with terminal alkynes

AU - Wan, Shun

AU - Wang, Sunewang R.

AU - Lu, Wenjun

PY - 2006/5/26

Y1 - 2006/5/26

N2 - Iodination of activated arenes by air-oxidation is carried out in the presence of catalytic bismuth salts at room temperature. Subsequently, the formed iodoarenes react with terminal alkynes to give arylalkynes under a selected palladium-catalyzed coupling condition in the same pot.

AB - Iodination of activated arenes by air-oxidation is carried out in the presence of catalytic bismuth salts at room temperature. Subsequently, the formed iodoarenes react with terminal alkynes to give arylalkynes under a selected palladium-catalyzed coupling condition in the same pot.

UR - https://www.scopus.com/pages/publications/33646923980

U2 - 10.1021/jo060424x

DO - 10.1021/jo060424x

M3 - 文章

C2 - 16709088

AN - SCOPUS:33646923980

SN - 0022-3263

VL - 71

SP - 4349

EP - 4352

JO - Journal of Organic Chemistry

JF - Journal of Organic Chemistry

IS - 11

ER -

One-pot preparation of arylalkynes by a tandem catalytic iodination of arenes and palladium-catalyzed coupling of iodoarenes with terminal alkynes

Abstract

Access to Document

Other files and links

Fingerprint

Cite this