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Journal article

Regio- and stereoselective hydrosilylation of immobilized terminal alkynes

From

Organic Chemistry, Department of Chemistry, Technical University of Denmark1

Department of Chemistry, Technical University of Denmark2

Regio- and stereoselective hydrosilylation of terminal alkynes on solid support using diisopropyl hydrosilanes yielding b-(E)-vinyl silanes with excellent selectivity is reported. The hydrosilylation is catalyzed by Pt(DVDS)/P(iBuNCH2CH2)3N (DVDS = 1,3-divinyl-1,1,3,3-tetramethyl-disiloxane), in which the bulky proazaphosphatrane ligand plays a key role for the selectivity.

The immobilized products are characterized with gel phase 13C NMR and 1H high resolution magic angle spinning NMR.

Language: English
Year: 2008
Pages: 6220-6223
ISSN: 18733581 and 00404039
Types: Journal article
DOI: 10.1016/j.tetlet.2008.08.043
ORCIDs: Gotfredsen, Charlotte Held and Clausen, Mads Hartvig

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