Homogeneous catalysis. Production of allyl alkyl sulphides by palladium mediated allylation
PR Auburn, J Whelan, B Bosnich
Index: Auburn, Pamela R.; Whelan, John; Bosnich, B. Journal of the Chemical Society, Chemical Communications, 1986 , # 2 p. 146 - 147
Full Text: HTML
Citation Number: 18
Abstract
The use of O-allyl S-alkyl dithiocarbonate substrates in palladium mediated catalytic allylation gives carbonyl sulphide and allyl alkyl sulphides with net retention of configuration and their use obviates the problems associated with sulphur nucleophiles in catalytic allylation.
Related Articles:
Isomerization of the Butenyl Methyl Sulfides with Methanethiol
[Huyser,E.S.; Kellogg,R.M. Journal of Organic Chemistry, 1965 , vol. 30, p. 2867 - 2868]
Organic sulfur compounds. VIII. Addition of thiols to conjugated diolefins
[Oswald,A.A. et al. Journal of the American Chemical Society, 1962 , vol. 84, p. 3897 - 3904]
Organic sulfur compounds. VIII. Addition of thiols to conjugated diolefins
[Oswald,A.A. et al. Journal of the American Chemical Society, 1962 , vol. 84, p. 3897 - 3904]
Isomerization of the Butenyl Methyl Sulfides with Methanethiol
[Huyser,E.S.; Kellogg,R.M. Journal of Organic Chemistry, 1965 , vol. 30, p. 2867 - 2868]
[Harano; Yamashiro; Misaka; Hisano Chemical and Pharmaceutical Bulletin, 1990 , vol. 38, # 11 p. 2956 - 2959]