Regiochemical control in the hydrostannylation of aryl substituted alkynes: A stereoselective synthesis of disubstituted vinylstannanes

Synlett

Volumn , Issue 2, 1999, Pages 246-248

  Liron, Frédéric ^a   Le Garrec, Pierre ^a   Alami, Mouâd ^a  

^a Ecl Sup Chim Organique Minerale   (France)

Author keywords

Aryl alkynes; Disubstituted vinylstannanes; Hydrostannylation reaction; Palladium

Indexed keywords

ALKYNE; TIN DERIVATIVE; UNCLASSIFIED DRUG; VINYLSTANNANE;

ARTICLE; CHEMICAL REACTION; ISOMER; STEREOCHEMISTRY; SYNTHESIS;

EID: 0032961554     PISSN: 09365214     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-1999-2576     Document Type: Article

References (15)

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13. 2 has been showm to have a dramatic influence on the regioselectivity of the hydrostannylation of disubstituted propargyl alcohols see: Greeves, N.; Torode, J.S. Synlett 1994, 537.
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15. 13C-NMR (50 MHz) δ: 148.20, 144.55, 140.55, 132.15, 127.75, 127.05, 126.65, 120.75, 60.70, 28.70, 27.20, 13.50, 10.45.