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Highly Efficient Cascade Reaction for Selective Formation of Spirocyclobutenes from Dienallenes via Palladium-Catalyzed Oxidative Double Carbocyclization-Carbonylation-Alkynylation

Qiu, Youai (author)
Stockholms universitet,Institutionen för organisk kemi
Yang, Bin (author)
Stockholms universitet,Institutionen för organisk kemi
Zhu, Can (author)
Stockholms universitet,Institutionen för organisk kemi
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Bäckvall, Jan-E. (author)
Stockholms universitet,Institutionen för organisk kemi
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 (creator_code:org_t)
2016-10-13
2016
English.
In: Journal of the American Chemical Society. - : American Chemical Society (ACS). - 0002-7863 .- 1520-5126. ; 138:42, s. 13846-13849
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • A highly selective cascade reaction that allows the direct transformation of dienallenes to spirocyclobutenes (spiro[3.4]octenes) as single diastereoisomers has been developed. The reaction involves formation of overall four C-C bonds and proceeds-via a palladium-catalyzed oxidative transformation with insertion of olefin, olefin, and carbon monoxide. Under slightly different reaction conditions, an additional CO insertion takes place to give spiro[4.4]nonenes with formation of overall five C-C bonds.

Subject headings

NATURVETENSKAP  -- Kemi -- Organisk kemi (hsv//swe)
NATURAL SCIENCES  -- Chemical Sciences -- Organic Chemistry (hsv//eng)

Keyword

organisk kemi
Organic Chemistry

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art (subject category)

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Qiu, Youai
Yang, Bin
Zhu, Can
Bäckvall, Jan-E.
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NATURAL SCIENCES
NATURAL SCIENCES
and Chemical Science ...
and Organic Chemistr ...
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Stockholm University

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