- Aromaticity and Relative Stabilities of Azines
[作者:WANG YAN; WU JUDY ICHIA; LI QIANSHU; SCHLEYER PAUL VON RAGUE,期刊:Organic Letters, 页码:4824-4827 , 文章类型: Article,,卷期:2010年12-21]
- The most refined nucleus-independent chemical shift index (NICS(0)(pi zz)) and the extra cyclic resonance energies (ECREs), based on the block localized wave function (BLW) method, show that the aromaticity of all azines...
- Synthesis and Characterization of Solution-Processable Core-Cyanated Perylene-3,4;9,10-bis(dicarboximide) Derivatives
[作者:ANDO SHINJI; FACCHETTI ANTONIO; MARKS TOBIN J,期刊:Organic Letters, 页码:4852-4855 , 文章类型: Article,,卷期:2010年12-21]
- Core-cyanated perylene-3,4;9,10-bis(carboxyimide) derivatives N-functionalized with tethered anthracenes (PDI3A-CN2, PDI4A-CN2) and the corresponding solution-processable cycloadduct precursors (PDI3A-CA-CN2, PDI4A-CA-CN...
- Efficient Generation of Biologically Active H-Pyrazolo[5,1-a]isoquinolines via Multicomponent Reaction
[作者:CHEN ZHIYUAN; WU JIE,期刊:Organic Letters, 页码:4856-4859 , 文章类型: Article,,卷期:2010年12-21]
- A highly efficient multicomponent reaction of 2-alkynylbenzaldehyde, sulfonohydrazide, alcohol, and alpha,beta-unsaturated aldehyde or ketone is disclosed, which generates the diverse H-pyrazolo[5,1-a]isoquinolines in go...
- Aromatization of Fulvene by Complexation with Lithium
[作者:OZIMINSKI W P; KRYGOWSKI T M; FOWLER P W; SONCINI A,期刊:Organic Letters, 页码:4880-4883 , 文章类型: Article,,卷期:2010年12-21]
- At the B3LYP/6-311++G(d,p) level, approach of a lithium atom to a face of the fulvene molecule leads to formation of a complex with binding energy 41 kcal/mol and significant ion-pair character. The fulvene moiety gains ...
- InCl3-Catalyzed Allylic Friedel-Crafts Reactions toward the Stereocontrolled Synthesis of 1,2,3,4-Tetrahydroquinolines
[作者:GIERA DAVID S; SCHNEIDER CHRISTOPH,期刊:Organic Letters, 页码:4884-4887 , 文章类型: Article,,卷期:2010年12-21]
- Allyl chlorides tethered to an N-aryl moiety readily undergo InCl3-catalyzed Friedel Crafts reactions to furnish highly enantiomerically enriched 1,2,3,4-tetrahydroquinolines with good yields and excellent diastereoselec...
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