- Catalytic Michael Reactions of Keto esters with a Camphor-Derived Acrylate Equivalent: Stereoselective Access to All-Carbon Quaternary Centers.
[作者:Palomo, Claudio;Oiarbide, Mikel;Garcia, Jesus M.;Banuelos, Patricia;Odriozola, Jose M.;Razkin, Jesus;Linden, Anthony;,期刊:Organic Letters, 页码:2637-2640 , 文章类型: 研究论文,,卷期:2008年10-13]
- A camphor-based a'-hydroxy enone reagent acts as a chiral acrylate equiv. in copper-catalyzed Michael reactions of b-keto esters and affords products, e.g. the (trimethylbicycloheptanyl)oxopentanoate I, that possess all-...
- Water-Soluble Tripeptide Ab (9-11) Forms Amyloid-Like Fibrils and Exhibits Neurotoxicity.
[作者:Naskar, Jishu;Drew, Michael G. B.;Deb, Ishani;Das, Sumantra;Banerjee, Arindam;,期刊:Organic Letters, 页码:2625-2628 , 文章类型: 研究论文,,卷期:2008年10-13]
- A water-sol., hydrophilic tripeptide GYE, having sequence identity with the N-terminal segment of amyloid peptides Ab(9-11), upon self-assocn. exhibits amyloid-like fibrils and significant neurotoxicity towards the Neuro...
- Electrophilic aromatic substitution reactions of 1,2-dihydro-1,2-azaborines. [Erratum to document cited in CA146:441839].
[作者:Pan, Jun;Kampf, Jeff W.;Ashe, Arthur J.;,期刊:Organic Letters, 页码:2917-2917 , 文章类型: 研究论文,,卷期:2008年10-13]
- On page 681, the Acknowledgement section should have included a statement thanking Mr. Joseph D. Davidson for performing some preliminary work on the bromination and deuteration of 1a.
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