| Year |
Citation |
Score |
| 2018 |
Krout MR, Henry CE, Jensen T, Wu KP, Virgil SC, Stoltz BM. Wolff/Cope Approach to the AB Ring of the Sesterterpenoid Variecolin. The Journal of Organic Chemistry. PMID 29298482 DOI: 10.1021/Acs.Joc.7B02972 |
0.718 |
|
| 2016 |
Zhang JM, Cui X, Chen QL, Wu KJ, Xu GH, He CH. Study on 2-bromo-7-chloromagnesio-9, 9-dioctylfluorene synthesis in a microreactor Gao Xiao Hua Xue Gong Cheng Xue Bao/Journal of Chemical Engineering of Chinese Universities. 30: 65-70. DOI: 10.3969/j.issn.1003-9015.2016.01.010 |
0.302 |
|
| 2014 |
Bai WJ, David JG, Feng ZG, Weaver MG, Wu KL, Pettus TR. The domestication of ortho-quinone methides. Accounts of Chemical Research. 47: 3655-64. PMID 25469551 DOI: 10.1021/Ar500330X |
0.693 |
|
| 2012 |
Liu WB, Yan Q, Liu FY, Tang XC, Chen HG, Liu J, Nie L, Zhang XW, Ji WK, Hu XH, Hu WF, Woodward Z, Wu KL, Wu MX, Liu XL, et al. Protein serine/threonine phosphotase-1 is essential in governing normal development of vertebrate eye. Current Molecular Medicine. 12: 1361-71. PMID 23016590 |
0.354 |
|
| 2012 |
Cohn EP, Wu KL, Pettus TR, Reich NO. A new strategy for detection and development of tractable telomerase inhibitors. Journal of Medicinal Chemistry. 55: 3678-86. PMID 22413845 DOI: 10.1021/Jm201191D |
0.59 |
|
| 2011 |
Wu KL, Mercado EV, Pettus TR. A convergent total synthesis of (±)-γ-rubromycin. Journal of the American Chemical Society. 133: 6114-7. PMID 21452818 DOI: 10.1021/Ja1115524 |
0.657 |
|
| 2011 |
Jackson SK, Wu K, Pettus TRR. ChemInform Abstract: Sequential Reactions Initiated by Oxidative Dearomatization. Biomimicry or Artifact? Cheminform. 42: no-no. DOI: 10.1002/chin.201152230 |
0.525 |
|
| 2011 |
Jackson SK, Wu KL, Pettus TRR. Sequential Reactions Initiated by Oxidative Dearomatization. Biomimicry or Artifact? Biomimetic Organic Synthesis. 2: 723-749. DOI: 10.1002/9783527634606.ch20 |
0.517 |
|
| 2009 |
Wu KL, Cohen EPMT, Huang Y, Pettus TRR. First total synthesis of malvone A and formal syntheses of boryquinone and hybocarpone using a concise strategy for construction of unsymmetrical naphthoquinones Synlett. 1273-1276. DOI: 10.1055/S-0028-1088134 |
0.633 |
|
| 2008 |
Marsini MA, Huang Y, Lindsey CC, Wu KL, Pettus TR. Diastereoselective syntheses of chroman spiroketals via [4 + 2] cycloaddition of enol ethers and o-quinone methides. Organic Letters. 10: 1477-80. PMID 18336038 DOI: 10.1021/Ol8003244 |
0.652 |
|
| 2007 |
Wu KL, Wilkinson S, Reich NO, Pettus TR. Facile synthesis of naphthoquinone spiroketals by diastereoselective oxidative [3 + 2] cycloaddition. Organic Letters. 9: 5537-40. PMID 18044909 DOI: 10.1021/Ol702450D |
0.641 |
|
| 2006 |
Lindsey CC, Wu KL, Pettus TR. Synthesis of electron deficient 5,6-aryloxy spiroketals. Organic Letters. 8: 2365-7. PMID 16706527 DOI: 10.1021/Ol0606886 |
0.709 |
|
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