Efficiency of a ruthenium catalyst in metathesis reactions of sulfur-containing compounds

Organic Letters

Volumn 4, Issue 10, 2002, Pages 1767-1770

  Spagnol, Gaëlle ^a   Heck, Marie Pierre ^a   Nolan, Steven P ^b   Mioskowski, Charles ^a,c  

^a CEA SACLAY   (France)

^b UNIVERSITY OF NEW ORLEANS   (United States)

^c UNIVERSITÉ DE STRASBOURG   (France)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE;

EID: 0001607220     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol025834w     Document Type: Article

References (63)

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56. When not commercially available, the diene sulfides were synthesized following the reported procedure: Bastien, G.; Surzur, J.-M. Bull. Soc. Chim. Fr. 1982, II, 84-88.
57. 2). Product formation and diene disappearance were monitored by integration of the allylic methylene picks. The formation of known cyclic product was confirmed by comparison with literature data. McIntosh, J. M. Can. J. Chem. 1978, 131-134. McIntosh, J. M.; Siddiqui, M. A. Can. J. Chem. 1983, 61, 1872-1875. Lozac'h, R., Braillon, B. J. Magn. Reson. 1973, 12, 244-260.
58. 2). Product formation and diene disappearance were monitored by integration of the allylic methylene picks. The formation of known cyclic product was confirmed by comparison with literature data. McIntosh, J. M. Can. J. Chem. 1978, 131-134. McIntosh, J. M.; Siddiqui, M. A. Can. J. Chem. 1983, 61, 1872-1875. Lozac'h, R., Braillon, B. J. Magn. Reson. 1973, 12, 244-260.
59. 2). Product formation and diene disappearance were monitored by integration of the allylic methylene picks. The formation of known cyclic product was confirmed by comparison with literature data. McIntosh, J. M. Can. J. Chem. 1978, 131-134. McIntosh, J. M.; Siddiqui, M. A. Can. J. Chem. 1983, 61, 1872-1875. Lozac'h, R., Braillon, B. J. Magn. Reson. 1973, 12, 244-260.
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62. NMR yield, 40% of starting substrate was recovered.
63. The unsaturated sulfide substrates were commercially available or were obtained after allylation of the corresponding thiols or following ref 21.