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Silaborations of 1,3-enynes - Substrate controlled allene/1,3-diene selectively
KTH, School of Chemical Science and Engineering (CHE), Chemistry, Organic Chemistry.ORCID iD: 0000-0002-1743-7650
2008 (English)In: Organic Letters, ISSN 1523-7060, E-ISSN 1523-7052, Vol. 10, no 12, 2505-2508 p.Article in journal (Refereed) Published
Abstract [en]

Silaboration of 1,3-enynes catalyzed by group 10 metal complexes affords 1,3-dienes with vinylborane and vinylsilane functions or 1,2-dienes with allylborane and vinylsilane functions. The type of product formed is determined by the size of the alkyne substituent.

Place, publisher, year, edition, pages
2008. Vol. 10, no 12, 2505-2508 p.
URN: urn:nbn:se:kth:diva-17605DOI: 10.1021/ol800768xISI: 000256762100045ScopusID: 2-s2.0-58349104339OAI: diva2:335649
QC 20100525Available from: 2010-08-05 Created: 2010-08-05Bibliographically approved

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Moberg, Christina
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