Literature DB >> 14527153

1,5-asymmetric induction of chirality using pi-allyltricarbonyliron lactone complexes: highly diastereoselective synthesis of alpha-functionalised carbonyl compounds.

Christopher J Hollowood1, Steven V Ley, Edward A Wright.   

Abstract

Silyl enol ethers derived from ketone functionalised rho-allyltricarbonyliron lactone complexes undergo highly diastereoselective carbon-fluorine and carbon-oxygen bond formation reactions with excellent control at the alpha-stereogenic centre.

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Year:  2003        PMID： 14527153     DOI： 10.1039/b306862e

Source DB:  PubMed          Journal:  Org Biomol Chem        ISSN： 1477-0520            Impact factor:   3.876


  2 in total

1.  1,5-Asymmetric induction during nucleophilic additions to arenetricarbonylchromium complexes: tricarbonyl(eta(6)-1-methyl-4-{spiro[(1R,2S)-1,7,7-trimethylbicyclo[2.2.1]heptane-3,2'-1,3-dioxolan]-2-yloxy}benzene)chromium.

Authors:  Harinandini Paramahamsan; Anthony J Pearson; Nathalie M Pinkerton; A Alan Pinkerton
Journal:  Acta Crystallogr C       Date:  2008-03-08       Impact factor: 1.172

2.  Nine New Gingerols from the Rhizoma of Zingiber officinale and Their Cytotoxic Activities.

Authors:  Zezhi Li; Yanzhi Wang; MeiLing Gao; Wanhua Cui; Mengnan Zeng; Yongxian Cheng; Juan Li
Journal:  Molecules       Date:  2018-02-02       Impact factor: 4.411
  2 in total

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