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A Suzuki-type cross-coupling reaction of arylacetylene halides with arylboronic acids

Shi, Yu (author)
Li, Xiaoyu (author)
Liu, Jianhui (author)
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Jiang, Wenfeng (author)
Sun, Licheng (author)
KTH,Organisk kemi
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 (creator_code:org_t)
2011-04-26
2011
English.
In: Applied organometallic chemistry. - : Wiley. - 0268-2605 .- 1099-0739. ; 25:7, s. 514-520
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • A PdCl(2)-catalyzed direct alkynylation of arylboronic acids to give diarylacetylenes is described. The optimal conditions using PdCl(2) as catalyst, MeOH-PhMe-H(2)O as solvent and K(2)CO(3) as base effectively suppressed the formation of homo-coupling product and afforded moderate to good yield of the desired unsymmetrical coupling product. This reaction represents a Suzuki-type sp(2)(C-B)-sp(C-X) cross-coupling.

Subject headings

NATURVETENSKAP  -- Kemi (hsv//swe)
NATURAL SCIENCES  -- Chemical Sciences (hsv//eng)

Keyword

Suzuki cross-coupling
diarylacetylene
palladium chloride
alkynylation
Chemistry
Kemi

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ref (subject category)
art (subject category)

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Shi, Yu
Li, Xiaoyu
Liu, Jianhui
Jiang, Wenfeng
Sun, Licheng
About the subject
NATURAL SCIENCES
NATURAL SCIENCES
and Chemical Science ...
Articles in the publication
Applied organome ...
By the university
Royal Institute of Technology

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