Asymmetric Pauson-Khand reactions using camphor-derived chelating thiols as chiral controllers

I Marchueta, E Montenegro, D Panov…

Index: Cookson,R.C.; Gopalan,R. Journal of the Chemical Society, Chemical Communications, 1978 , p. 924 - 925

Full Text: HTML

Citation Number: 46

Abstract

... The Journal of ... The synthesis of ethynyl sulfide 7a was initially accomplished using the methodology developed by Cookson. 19 Thus, the sodium thiolate of 1a was treated with 2-bromoacetaldehyde diethylacetal affording 1,1-diethoxy-2-(R*-thio)ethane 6a in 80% yield. ...

Related Articles:

Geometrically specific hydrogen transfer in the reaction of terminally alkyl-substituted 1, 3-dienes with 1, 4-quinones

[Cameron, Donald W.; Heisey, Ross M. Australian Journal of Chemistry, 2000 , vol. 53, # 2 p. 109 - 121]

Palladium-catalyzed three carbon chain extension reactions with acrolein acetals. A convenient synthesis of conjugated dienals

[Patel, Babu A.; Kim, Jin-Il I.; Bender, Diana D.; Kao, Lien-Chung; Heck, Richard F. Journal of Organic Chemistry, 1981 , vol. 46, # 6 p. 1061 - 1067]

Geometrically specific hydrogen transfer in the reaction of terminally alkyl-substituted 1, 3-dienes with 1, 4-quinones

[Cameron, Donald W.; Heisey, Ross M. Australian Journal of Chemistry, 2000 , vol. 53, # 2 p. 109 - 121]

More Articles...