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Journal Abstract Search

1024 related items for PubMed ID: 18558688

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  • 5. Theoretical elucidation of Au(I)-catalyzed cycloisomerizations of cycloalkyl-substituted 1,5-enynes: 1,2-alkyl shift versus C-H bond insertion products.
    Liu Y, Zhang D, Zhou J, Liu C.
    J Phys Chem A; 2010 May 27; 114(20):6164-70. PubMed ID: 20433188
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  • 6. A theoretical study on the complete catalytic cycle of the hetero-Pauson-Khand-type [2+2+1] cycloaddition reaction of ketimines, carbon monoxide and ethylene catalyzed by iron carbonyl complexes.
    Imhof W, Anders E, Göbel A, Görls H.
    Chemistry; 2003 Mar 03; 9(5):1166-81. PubMed ID: 12596153
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  • 12. Theoretical analysis of mechanistic pathways for hydrogen evolution catalyzed by cobaloximes.
    Solis BH, Hammes-Schiffer S.
    Inorg Chem; 2011 Nov 07; 50(21):11252-62. PubMed ID: 21942543
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  • 13. Kinetics study and theoretical modeling of the Diels-Alder reactions of cyclopentadiene and cyclohexadiene with methyl vinyl ketone. The effects of a novel organotungsten catalyst.
    Fu YS, Tsai SC, Huang CH, Yen SY, Hu WP, Yu SJ.
    J Org Chem; 2003 Apr 18; 68(8):3068-77. PubMed ID: 12688774
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  • 14. Remote substituent effects in ruthenium-catalyzed [2+2] cycloadditions: an experimental and theoretical study.
    Liu P, Jordan RW, Kibbee SP, Goddard JD, Tam W.
    J Org Chem; 2006 May 12; 71(10):3793-803. PubMed ID: 16674052
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  • 15. Reaction mechanism and stereoselectivity of ruthenium--porphyrin-catalyzed intramolecular amidation of sulfamate ester: a DFT computational study.
    Lin X, Che CM, Phillips DL.
    J Org Chem; 2008 Jan 18; 73(2):529-37. PubMed ID: 18092803
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  • 17. A DFT study on the regioselectivity of the reaction of dichloropropynylborane with isoprene.
    Silva MA, Pellegrinet SC, Goodman JM.
    J Org Chem; 2003 May 16; 68(10):4059-66. PubMed ID: 12737591
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  • 20. Density functional study on the reaction mechanism of palladium-catalyzed addition of cyanoboranes to alkynes.
    Wang MY, Cheng L, Wu ZJ.
    J Comput Chem; 2008 Aug 16; 29(11):1825-39. PubMed ID: 18351592
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