| Year |
Citation |
Score |
| 2008 |
Jain HD, Zhang C, Zhou S, Zhou H, Ma J, Liu X, Liao X, Deveau AM, Dieckhaus CM, Johnson MA, Smith KS, Macdonald TL, Kakeya H, Osada H, Cook JM. Synthesis and structure-activity relationship studies on tryprostatin A, an inhibitor of breast cancer resistance protein. Bioorganic & Medicinal Chemistry. 16: 4626-51. PMID 18321710 DOI: 10.1016/J.Bmc.2008.02.050 |
0.698 |
|
| 2007 |
Han D, Försterling FH, Deschamps JR, Parrish D, Liu X, Yin W, Huang S, Cook JM. Conformational analysis of the cis- and trans-adducts of the Pictet - Spengler reaction. Evidence for the structural basis for the C(1) - N(2) scission process in the cis- to trans-isomerization. Journal of Natural Products. 70: 75-82. PMID 17253853 DOI: 10.1021/Np060391G |
0.7 |
|
| 2004 |
Liu X, Hartwig JF. Palladium-catalyzed arylation of trimethylsilyl enolates of esters and imides. High functional group tolerance and stereoselective synthesis of alpha-aryl carboxylic acid derivatives. Journal of the American Chemical Society. 126: 5182-91. PMID 15099101 DOI: 10.1021/Ja031544E |
0.38 |
|
| 2003 |
Hama T, Liu X, Culkin DA, Hartwig JF. Palladium-catalyzed alpha-arylation of esters and amides under more neutral conditions. Journal of the American Chemical Society. 125: 11176-7. PMID 16220921 DOI: 10.1021/Ja036792P |
0.338 |
|
| 2003 |
Yu J, Wang T, Liu X, Deschamps J, Flippen-Anderson J, Liao X, Cook JM. General approach for the synthesis of sarpagine indole alkaloids. Enantiospecific total synthesis of (+)-vellosimine, (+)-normacusine B, (-)-alkaloid Q3, (-)-panarine, (+)-Na-methylvellosimine, and (+)-Na-methyl-16-epipericyclivine. The Journal of Organic Chemistry. 68: 7565-81. PMID 14510528 DOI: 10.1021/Jo030006H |
0.667 |
|
| 2003 |
Liu X, Hartwig JF. Palladium-catalyzed alpha-arylation of azlactones to form quaternary amino acid derivatives. Organic Letters. 5: 1915-8. PMID 12762685 DOI: 10.1021/Ol034570Q |
0.302 |
|
| 2003 |
Cao H, Yu J, Wearing XZ, Zhang C, Liu X, Deschamps J, Cook JM. The first enantiospecific synthesis of (-)-koumidine via the intramolecular palladium-catalyzed enolate driven cross coupling reaction. The stereospecific introduction of the 19-(Z) ethylidene side chain Tetrahedron Letters. 44: 8013-8017. DOI: 10.1016/J.Tetlet.2003.08.072 |
0.725 |
|
| 2002 |
Jørgensen M, Lee S, Liu X, Wolkowski JP, Hartwig JF. Efficient synthesis of alpha-aryl esters by room-temperature palladium-catalyzed coupling of aryl halides with ester enolates. Journal of the American Chemical Society. 124: 12557-65. PMID 12381200 DOI: 10.1021/Ja027643U |
0.341 |
|
| 2002 |
Liu X, Deschamp JR, Cook JM. Regiospecific, enantiospecific total synthesis of the alkoxy-substituted indole bases, 16-epi-N(a)-methylgardneral, 11-methoxyaffinisine, and 11-methoxymacroline as well as the indole alkaloids alstophylline and macralstonine. Organic Letters. 4: 3339-42. PMID 12323013 DOI: 10.1021/Ol020101X |
0.637 |
|
| 2002 |
Liu X, Zhang C, Liao X, Cook JM. Enantiospecific total synthesis of the enantiomer of the indole alkaloid intermediate macroline Tetrahedron Letters. 43: 7373-7377. DOI: 10.1016/S0040-4039(02)01729-X |
0.754 |
|
| 2001 |
Liu X, Cook JM. General approach for the synthesis of sarpagine/macroline indole alkaloids. Enantiospecific total synthesis of the indole alkaloid trinervine. Organic Letters. 3: 4023-6. PMID 11735575 DOI: 10.1021/Ol0101990 |
0.633 |
|
| 2001 |
Wang T, Xu Q, Yu P, Liu X, Cook JM. Stereocontrolled total synthesis of alkaloid G via the oxy-anion Cope rearrangement and improved total synthesis of (+)-ajmaline. Organic Letters. 3: 345-8. PMID 11428010 DOI: 10.1021/Ol000331G |
0.572 |
|
| 2001 |
Ma C, Liu X, Li X, Flippen-Anderson J, Yu S, Cook JM. Efficient asymmetric synthesis of biologically important tryptophan analogues via a palladium-mediated heteroannulation reaction. The Journal of Organic Chemistry. 66: 4525-42. PMID 11421771 DOI: 10.1021/Jo001679S |
0.775 |
|
| 2000 |
Liu X, Wang T, Xu Q, Ma C, Cook JM. Enantiospecific total synthesis of the enantiomer of the indole alkaloid affinisine Tetrahedron Letters. 41: 6299-6303. DOI: 10.1016/S0040-4039(00)01061-3 |
0.755 |
|
| 2000 |
Ma C, Yu S, He X, Liu X, Cook JM. Efficient asymmetric synthesis of important tryptophan analogs for biological research via the Schollkopf chiral auxiliary Tetrahedron Letters. 41: 2781-2785. DOI: 10.1016/S0040-4039(00)00263-X |
0.738 |
|
| 1999 |
Ma C, He X, Liu X, Yu S, Zhao S, Cook JM. Effect of the leaving group on the alkylation diastereoselectivity of the Schollkopf chiral auxiliary Tetrahedron Letters. 40: 2917-2918. DOI: 10.1016/S0040-4039(99)00394-9 |
0.717 |
|
| 1999 |
Ma C, Liu X, Yu S, Zhao S, Cook JM. Concise synthesis of optically active ring-A substituted tryptophans Tetrahedron Letters. 40: 657-660. DOI: 10.1016/S0040-4039(98)02497-6 |
0.753 |
|
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