- Fluorescent chemosensor for chloroalkanes.
[作者:Lee, Jung-Jae;Noll, Bruce C.;Smith, Bradley D.;,期刊:Organic Letters, 页码:1735-1738 , 文章类型: 研究论文,,卷期:2008年10-9]
- Two structurally related macrocyclic amines with naphthalene groups (I, R=CH2, CO) act as fluorescent dosimeters for reactive chloroalkanes, including the common industrial solvent dichloromethane. The macrocyclic struc...
- Gas-Phase Stereoselective Binding to Mn/Salen Catalysts.
[作者:Fagin, Adelaide E.;Wang, Guoping;Lau, Michel C.;Gronert, Scott;,期刊:Organic Letters, 页码:1771-1773 , 文章类型: 研究论文,,卷期:2008年10-9]
- Gas-phase equil. measurements were used to det. the stereoselectivity of binding the enantiomers of 1-phenylethanol to Mn/salen asym. epoxidn. catalysts. There is significant selectivity in the gas-phase binding, and th...
- Diastereoselective Synthesis of d-Amino acids through Domino Ireland-Claisen Rearrangement and Michael Addition.
[作者:Garrido, Narciso M.;Garcia, Mercedes;Diez, David;Sanchez, M. Rosa;Sanz, F.;Urones, Julio G.;,期刊:Organic Letters, 页码:1687-1690 , 文章类型: 研究论文,,卷期:2008年10-9]
- rearrangement and asym. Michael addn. - is described. A protocol starting from Baylis-Hillman adducts, e.g. R1CH:C(CH2OAc)CO2R2 (R1 = Ph, 3,4-(MeO)2C6H3, 3-pyridinyl, R2 = Me, tert-Bu), using a chiral lithium amide affo...
- Rhodium-Catalyzed Anti Selective Cross-Addition of Bis(trimethylsilyl)acetylene to Diarylacetylenes via Carbon-Silicon Bond Cleavage.
[作者:Horita, Akinobu;Tsurugi, Hayato;Satoh, Tetsuya;Miura, Masahiro;,期刊:Organic Letters, 页码:1751-1754 , 文章类型: 研究论文,,卷期:2008年10-9]
- The addn. of bis(trimethylsilyl)acetylene to diarylacetylenes RCYCR (R = Ph, 4-ClC6H4, 4-MeOC6H4, 2-thienyl) proceeds efficiently and selectively in a formal anti fashion in the presence of [Rh(OH)(cod)]2/bisphosphine an...
- Mo-Au Combo Catalysis for Rapid 1,3-Rearrangement of Propargyl Alcohols into a,b-Unsaturated Carbonyl Compounds.
[作者:Egi, Masahiro;Yamaguchi, Yoshiko;Fujiwara, Noboru;Akai, Shuji;,期刊:Organic Letters, 页码:1867-1870 , 文章类型: 研究论文,,卷期:2008年10-9]
- The combination of Mo and cationic Au catalysts dramatically accelerated the rearrangement of diverse propargyl alcs., which includes a short reaction time, mild conditions, and high product yields. A practical applicati...
- Asymmetric direct aldol reactions of pyruvic derivatives.
[作者:Luo, Sanzhong;Xu, Hui;Chen, Liujuan;Cheng, Jin-Pei;,期刊:Organic Letters, 页码:1775-1778 , 文章类型: 研究论文,,卷期:2008年10-9]
- as I/TfOH, can effectively catalyze the direct aldol reactions of pyruvic derivs. with aldehydes. The reaction proceeded with excellent syn diastereoselectivities and enantioselectivities, thus functionally mimicking th...
- Structure and semisynthesis of platensimide A, produced by Streptomyces platensis.
[作者:Herath, Kithsiri B.;Zhang, Chaowei;Jayasuriya, Hiranthi;Ondeyka, John G.;Zink, Deborah L.;Burgess, Bruce;Wang, Jun;Singh, Sheo B.;,期刊:Organic Letters, 页码:1699-1702 , 文章类型: 研究论文,,卷期:2008年10-9]
- Platensimycin and platencin are novel natural product antibiotics that inhibit bacterial growth by inhibiting condensing enzymes FabF and FabF/FabH of fatty acid biosynthesis pathways, resp. Continued search for the nat...
- Oxidation of a Biomarker for Phenol Carcinogen Exposure: Expanding the Redox Chemistry of 2'-Deoxyguanosine.
[作者:Weishar, Jennifer L.;McLaughlin, Christopher K.;Baker, Michael;Gabryelski, Wojciech;Manderville, Richard A.;,期刊:Organic Letters, 页码:1839-1842 , 文章类型: 研究论文,,卷期:2008年10-9]
- A biomarker for phenolic carcinogen exposure, 8-(4''-hydroxyphenyl)-2'-deoxyguanosine, has been found to undergo oxidative coupling in the presence of Na2IrCl6 to afford ortho-ortho C-C-coupled polyphenols through the in...
- Enantioselective Synthesis of Iridal, the Parent Molecule of the Iridal Triterpenoid Class.
[作者:Corbu, Andrei;Aquino, Maurizio;Pratap, T. V.;Retailleau, Pascal;Arseniyadis, Simeon;,期刊:Organic Letters, 页码:1787-1790 , 文章类型: 研究论文,,卷期:2008年10-9]
- approach that allows access for several representatives of the iridal family as well as diversely substituted analogs. The success of the proposed synthetic plan depends upon the effortless stereoselective establishment...
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