Year |
Citation |
Score |
2015 |
Mao YP, Yin WJ, Guo R, Zhang GS, Fang JL, Chi F, Qi ZY, Liu MZ, Ma J, Sun Y. Dosimetric benefit to organs at risk following margin reductions in nasopharyngeal carcinoma treated with intensity-modulated radiation therapy. Chinese Journal of Cancer. 34: 16. PMID 26058563 DOI: 10.1186/s40880-015-0016-8 |
0.36 |
|
2011 |
Shi YK, Yang S, Han XH, Ma J, Ren HY, Cen XN, Zhou SY, Wang C, Jiang WQ, Huang HQ, Wang JM, Zhu J, Chen H, Han MZ, Huang H, et al. [A prospective multicenter study of rituximab combined with high-dose chemotherapy and autologous peripheral blood stem cell transplantation for aggressive B-cell lymphoma]. Zhonghua Zhong Liu Za Zhi [Chinese Journal of Oncology]. 31: 592-6. PMID 20021946 |
0.417 |
|
2010 |
Yin W, Kabir MS, Wang Z, Rallapalli SK, Ma J, Cook JM. Enantiospecific total synthesis of the important biogenetic intermediates along the ajmaline pathway, (+)-polyneuridine and (+)-polyneuridine aldehyde, as well as 16-epivellosimine and macusine A. The Journal of Organic Chemistry. 75: 3339-49. PMID 20392128 DOI: 10.1021/Jo100279W |
0.676 |
|
2009 |
Ma J, Yin W, Zhou H, Liao X, Cook JM. General approach to the total synthesis of 9-methoxy-substituted indole alkaloids: synthesis of mitragynine, as well as 9-methoxygeissoschizol and 9-methoxy-N(b)-methylgeissoschizol. The Journal of Organic Chemistry. 74: 264-73. PMID 19046119 DOI: 10.1021/Jo801839T |
0.702 |
|
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 |
0.662 |
|
2007 |
Ma J, Yin W, Zhou H, Cook JM. Total synthesis of the opioid agonistic indole alkaloid mitragynine and the first total syntheses of 9-methoxygeissoschizol and 9-methoxy-Nb-methylgeissoschizol. Organic Letters. 9: 3491-4. PMID 17685530 DOI: 10.1021/Ol071220L |
0.624 |
|
2007 |
Yin W, Ma J, Rivas FM, Cook JM. First enantiospecific total synthesis of the important biogenetic intermediates, (+)-polyneuridine and (+)-polyneuridine aldehyde, as well as 16-epi-vellosimine and macusine A. Organic Letters. 9: 295-8. PMID 17217288 DOI: 10.1021/Ol062762Q |
0.669 |
|
2007 |
Yin W, Ma J, Rivas FM, Cook JM. First Enantiospecific Total Synthesis of the Important Biogenetic Intermediates, (+)-Polyneuridine(Ia) and (+)-Polyneuridine Aldehyde(IIa), as well as 16-Epi-vellosimine (IIb) and Macusine A (Ib). Cheminform. 38. DOI: 10.1002/chin.200721177 |
0.63 |
|
2006 |
Zhou H, Liao X, Yin W, Ma J, Cook JM. General approach for the synthesis of 12-methoxy-substituted sarpagine indole alkaloids including (-)-12-methoxy-N(b)-methylvoachalotine, (+)-12-methoxy-N(a)-methylvellosimine, (+)-12-methoxyaffinisine, and (-)-fuchsiaefoline. The Journal of Organic Chemistry. 71: 251-9. PMID 16388644 DOI: 10.1021/Jo052081T |
0.699 |
|
2005 |
Liao X, Zhou H, Wearing XZ, Ma J, Cook JM. The first regiospecific, enantiospecific total synthesis of 6-oxoalstophylline and an improved total synthesis of alstonerine and alstophylline as well as the bisindole alkaloid macralstonine. Organic Letters. 7: 3501-4. PMID 16048327 DOI: 10.1021/Ol051208Y |
0.596 |
|
2005 |
Yin W, Sarma PVVS, Ma J, Han D, Chen JL, Cook JM. Synthesis of bivalent ligands of β-carboline-3-carboxylates via a palladium-catalyzed homocoupling process Tetrahedron Letters. 46: 6363-6368. DOI: 10.1016/J.Tetlet.2005.07.022 |
0.571 |
|
2003 |
Yu J, Wang T, Wearing XZ, Ma J, Cook JM. Enantiospecific total synthesis of (-)-(E)16-epiaffinisine, (+)-(E)16-epinormacusine B, and (+)-dehydro-16-epiaffinisine as well as the stereocontrolled total synthesis of alkaloid G. The Journal of Organic Chemistry. 68: 5852-9. PMID 12868917 DOI: 10.1021/Jo030116O |
0.544 |
|
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