Year |
Citation |
Score |
2020 |
Geng S, Zhang J, Chen S, Liu Z, Zeng X, He Y, Feng Z. Development and Mechanistic Studies of Iron-Catalyzed Construction of Csp-B Bonds via C-O Bond Activation. Organic Letters. PMID 32585109 DOI: 10.1021/Acs.Orglett.0C01937 |
0.323 |
|
2020 |
Zhao S, Zang ZL, Li S, Wen X, Wang C, Guo J, He Y. Iridium-Catalyzed Cycloisomerization of N-Tethered 1,7-Enynes: Construction of Azabicyclo [5.1.0] octene System. The Journal of Organic Chemistry. PMID 32551602 DOI: 10.1021/Acs.Joc.0C00516 |
0.358 |
|
2019 |
Mao CL, Zhao S, Zang ZL, Xiao L, Zhou CH, He Y, Cai GX. Pd-Catalyzed remote site- and stereo-selective C(alkenyl)-H alkenylation of unactivated cycloalkenes. The Journal of Organic Chemistry. PMID 31829008 DOI: 10.1021/Acs.Joc.9B02797 |
0.316 |
|
2019 |
Lagishetti C, Banne S, You H, Tang M, Guo J, Qi N, He Y. Construction of Bridged-Ring-Fused Naphthalenone Derivatives Through an Unexpected Zn(OTf)-Catalyzed Cascade Transformation. Organic Letters. PMID 31247780 DOI: 10.1021/Acs.Orglett.9B01912 |
0.31 |
|
2019 |
Allu SR, Banne S, Jiang J, Qi N, Guo J, He Y. A Unified Synthetic Approach to Optically Pure Curvularin-type Metabolites. The Journal of Organic Chemistry. PMID 31083915 DOI: 10.1021/Acs.Joc.9B00776 |
0.33 |
|
2019 |
Liu Y, Wang Z, Banne S, Guo J, He Y. Towards the Total Synthesis of Scabrosins: Synthesis of Desulfur-scabrosins Skeleton and Its Stereoisomers. The Journal of Organic Chemistry. PMID 30900891 DOI: 10.1021/Acs.Joc.9B00015 |
0.395 |
|
2019 |
Wu Q, Shao P, He Y. Synthesis of 1,4,5,6-tetrahydropyridazines and pyridazines via transition-metal-free (4 + 2) cycloaddition of alkoxyallenes with 1,2-diaza-1,3-dienes Rsc Advances. 9: 21507-21512. DOI: 10.1039/C9Ra02712B |
0.345 |
|
2018 |
Lin Z, Xu X, Zhao S, Yang X, Guo J, Zhang Q, Jing C, Chen S, He Y. Total synthesis and antimicrobial evaluation of natural albomycins against clinical pathogens. Nature Communications. 9: 3445. PMID 30181560 DOI: 10.1038/S41467-018-05821-1 |
0.325 |
|
2018 |
Addepalli Y, Yu Z, Ji J, Zou C, Wang Z, He Y. Tandem Diels-Alder/oxidation-aromatization reactions involving 2-styrylchromones and arynes. Organic & Biomolecular Chemistry. PMID 30091440 DOI: 10.1039/C8Ob01199K |
0.323 |
|
2018 |
Zhang N, Yu Z, Yang X, Zhou Y, Tang Q, Hu P, Wang J, Zhang SL, Wang MW, He Y. Difuran-substituted quinoxalines as a novel class of PI3Kα H1047R mutant inhibitors: Synthesis, biological evaluation and structure-activity relationship. European Journal of Medicinal Chemistry. 157: 37-49. PMID 30071408 DOI: 10.1016/J.Ejmech.2018.07.061 |
0.316 |
|
2018 |
Wang ZP, He Y, Shao PL. Transition-metal-free synthesis of polysubstituted pyrrole derivatives via cyclization of methyl isocyanoacetate with aurone analogues. Organic & Biomolecular Chemistry. PMID 30028468 DOI: 10.1039/C8Ob01558A |
0.312 |
|
2018 |
Wang ZP, Xiang S, Shao PL, He Y. Catalytic Asymmetric [3 + 2] Cycloaddition Reaction Between Aurones and Isocyanoacetates: Access to Spiropyrrolines via Silver Catalysis. The Journal of Organic Chemistry. PMID 29991251 DOI: 10.1021/Acs.Joc.8B01622 |
0.348 |
|
2018 |
Li S, Li G, Yang X, Meng Q, Yuan S, He Y, Sun D. Design, synthesis and biological evaluation of artemisinin derivatives containing fluorine atoms as anticancer agents. Bioorganic & Medicinal Chemistry Letters. PMID 29789258 DOI: 10.1016/J.Bmcl.2018.05.035 |
0.305 |
|
2018 |
Zhou M, Su Q, Addepalli Y, He Y, Wang Z. An asymmetric Mannich reaction of α-diazocarbonyl compounds and N-sulfonyl cyclic ketimines catalyzed by complexes generated from chiral and achiral phosphines with gold(i). Organic & Biomolecular Chemistry. PMID 29620118 DOI: 10.1039/C8Ob00577J |
0.343 |
|
2018 |
Addepalli Y, Yang X, Zhou M, Reddy DP, Zhang SL, Wang Z, He Y. Synthesis and anticancer activity evaluation of novel azacalix[2]arene[2]pyrimidines. European Journal of Medicinal Chemistry. 151: 214-225. PMID 29614418 DOI: 10.1016/J.Ejmech.2018.02.079 |
0.308 |
|
2018 |
Zhang N, Yu Z, Yang X, Hu P, He Y. Synthesis of novel ring-contracted artemisinin dimers with potent anticancer activities. European Journal of Medicinal Chemistry. 150: 829-840. PMID 29597166 DOI: 10.1016/J.Ejmech.2018.03.010 |
0.319 |
|
2018 |
You H, Vegi SR, Lagishetti C, Chen S, Reddy RS, Yang X, Guo J, Wang C, He Y. Synthesis of Bioactive 3,4-Dihydro-2H-naphtho[2,3-b][1,4]oxazine-5,10-dione and 2,3,4,5-Tetrahydro-1H-naphtho[2,3-b]azepine-6,11-dione Derivatives via Copper-catalysed Intramolecular Coupling Reaction. The Journal of Organic Chemistry. PMID 29546756 DOI: 10.1021/Acs.Joc.8B00020 |
0.353 |
|
2018 |
Wang Z, Addepalli Y, He Y. Construction of Polycyclic Indole Derivatives via Multiple Aryne Reactions with Azaheptafulvenes. Organic Letters. PMID 29336163 DOI: 10.1021/Acs.Orglett.7B03789 |
0.347 |
|
2018 |
Xiong B, Zeng X, Geng S, Chen S, He Y, Feng Z. Thiyl radical promoted chemo- and regioselective oxidation of CC bonds using molecular oxygen via iron catalysis Green Chemistry. 20: 4521-4527. DOI: 10.1039/C8Gc02369G |
0.3 |
|
2018 |
Wang Z, Wu Q, Jiang J, Li Z, Peng X, Shao P, He Y. Catalytic asymmetric synthesis of pyrrolidine derivatives bearing heteroatom-substituted quaternary stereocenters Organic Chemistry Frontiers. 5: 36-40. DOI: 10.1039/C7Qo00692F |
0.362 |
|
2017 |
Karnakanti S, Zang ZL, Zhao S, Shao PL, Hu P, He Y. Palladium-catalyzed oxidative arylacetoxylation of alkenes: synthesis of indole and indoline derivatives. Chemical Communications (Cambridge, England). PMID 28956559 DOI: 10.1039/C7Cc06448A |
0.312 |
|
2017 |
Prabhakar Reddy D, Zhang N, Yu Z, Wang Z, He Y. Total Synthesis of Kanamienamide. The Journal of Organic Chemistry. PMID 28944669 DOI: 10.1021/Acs.Joc.7B01984 |
0.382 |
|
2017 |
Shao PL, Li ZR, Wang ZP, Zhou MH, Wu Q, Hu P, He Y. [3 + 2] Cycloaddition of Azaoxyallyl Cations with Cyclic Ketones: Access to Spiro-4-oxazolidinones. The Journal of Organic Chemistry. PMID 28925693 DOI: 10.1021/Acs.Joc.7B01728 |
0.349 |
|
2017 |
Banne S, Prabhakar Reddy D, Li W, Wang C, Guo J, He Y. A Unified Modular Synthetic Strategy for Dictyodendrins F, H, I, and G. Organic Letters. PMID 28846426 DOI: 10.1021/Acs.Orglett.7B02511 |
0.35 |
|
2017 |
Liu Q, Hu P, He Y. Asymmetric Total Synthesis of Nannocystin A. The Journal of Organic Chemistry. PMID 28787157 DOI: 10.1021/Acs.Joc.7B01502 |
0.328 |
|
2017 |
Wang Z, Xu H, Su Q, Hu P, Shao PL, He Y, Lu Y. Enantioselective Synthesis of Tetrahydropyridines/Piperidines via Stepwise [4 + 2]/[2 + 2] Cyclizations. Organic Letters. PMID 28560873 DOI: 10.1021/Acs.Orglett.7B01221 |
0.37 |
|
2017 |
Zang ZL, Karnakanti S, Zhao S, Hu P, Wang Z, Shao PL, He Y. Synthesis of Spiro-dihydroquinoline and Octahydrophenanthrene Derivatives via Palladium-Catalyzed Intramolecular Oxidative Arylation. Organic Letters. PMID 28267344 DOI: 10.1021/Acs.Orglett.7B00228 |
0.333 |
|
2017 |
Kiran IN, Reddy RS, Lagishetti C, Xu H, Wang Z, He Y. Selective Aza Diels-Alder and Domino [4+2]/[2+2] Cycloaddition Reactions of Arynes with N-Sulfonyl Ketimines. The Journal of Organic Chemistry. PMID 28097867 DOI: 10.1021/Acs.Joc.6B02667 |
0.334 |
|
2017 |
Peng X, Ho YA, Wang Z, Shao P, Zhao Y, He Y. Formal [3 + 2] cycloaddition of α-unsubstituted isocyanoacetates and methyleneindolinones: enantioselective synthesis of spirooxindoles Organic Chemistry Frontiers. 4: 81-85. DOI: 10.1039/C6Qo00555A |
0.319 |
|
2016 |
Qi N, Wang Z, Allu SR, Liu Q, Guo J, He Y. Total Syntheses of Anti-HIV Cyclodepsipeptides Aetheramides A and B. The Journal of Organic Chemistry. 81: 12466-12471. PMID 27978762 DOI: 10.1021/Acs.Joc.6B02292 |
0.344 |
|
2016 |
Qi N, Allu SR, Wang Z, Liu Q, Guo J, He Y. Asymmetric Total Syntheses of Aetheramides and Their Stereoisomers: Stereochemical Assignment of Aetheramides. Organic Letters. PMID 27603759 DOI: 10.1021/Acs.Orglett.6B02371 |
0.362 |
|
2016 |
Reddy RS, Lagishetti C, Chen S, Kiran IN, He Y. Synthesis of Dihydrophenanthridines and Oxoimidazolidines from Anilines and Ethylglyoxylate via Aza Diels-Alder Reaction of Arynes and KF-Induced Annulation. Organic Letters. PMID 27571345 DOI: 10.1021/Acs.Orglett.6B02186 |
0.345 |
|
2016 |
Santhosh Reddy R, Lagishetti C, Kiran IN, You H, He Y. Transition-Metal-Free Cascade Synthesis of 4-Quinolones: Umpolung of Michael Acceptors via Ene Reaction with Arynes. Organic Letters. PMID 27434217 DOI: 10.1021/Acs.Orglett.6B01830 |
0.318 |
|
2016 |
Guo J, Kiran IN, Reddy RS, Gao J, Tang M, Liu Y, He Y. Synthesis of Carbazolequinones by Formal [3 + 2] Cycloaddition of Arynes and 2-Aminoquinones. Organic Letters. PMID 27149368 DOI: 10.1021/Acs.Orglett.6B01090 |
0.361 |
|
2016 |
He Y, Agarwal PK, Kiran IN, Yu R, Cao B, Zou C, Zhou X, Xu H, Xu B, Zhu L, Lan Y, Nicolaou KC. Efficient Synthesis of Dimeric Oxazoles, Piperidines and Tetrahydroisoquinolines from N-Substituted 2-Oxazolones. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 27113382 DOI: 10.1002/Chem.201601471 |
0.476 |
|
2016 |
Reddy RS, Zheng S, Lagishetti C, You H, He Y. A practical and efficient route to heteraphanes: synthesis of structurally simplified analogues of ansamycins Rsc Advances. 6: 68199-68203. DOI: 10.1039/C6Ra16247A |
0.374 |
|
2016 |
Guo J, Kiran INC, Gao J, Reddy RS, He Y. Total synthesis of calothrixins and their analogues via formal [3+2] cycloaddition of arynes and 2-aminophenanthridinedione Tetrahedron Letters. 57: 3481-3484. DOI: 10.1016/J.Tetlet.2016.06.091 |
0.367 |
|
2016 |
He Y, Agarwal PK, Kiran INC, Yu R, Cao B, Zou C, Zhou X, Xu H, Xu B, Zhu L, Lan Y, Nicolaou KC. Frontispiece: Efficient Synthesis of Dimeric Oxazoles, Piperidines and Tetrahydroisoquinolines from N -Substituted 2-Oxazolones Chemistry: a European Journal. 22. DOI: 10.1002/Chem.201682361 |
0.455 |
|
2008 |
Huang S, Liu Z, Tian SS, Sandberg M, Spalding TA, Romeo R, Iskandar M, Wang Z, Karanewsky D, He Y. Discovery of 2-amino-6-carboxamidobenzothiazoles as potent Lck inhibitors. Bioorganic & Medicinal Chemistry Letters. 18: 2324-8. PMID 18353642 DOI: 10.1016/J.Bmcl.2008.02.079 |
0.32 |
|
2005 |
Liu H, Tully DC, Epple R, Bursulaya B, Li J, Harris JL, Williams JA, Russo R, Tumanut C, Roberts MJ, Alper PB, He Y, Karanewsky DS. Design and synthesis of arylaminoethyl amides as noncovalent inhibitors of cathepsin S. Part 1. Bioorganic & Medicinal Chemistry Letters. 15: 4979-84. PMID 16183279 DOI: 10.1016/J.Bmcl.2005.08.017 |
0.314 |
|
2004 |
Molteni V, He X, Nabakka J, Yang K, Kreusch A, Gordon P, Bursulaya B, Warner I, Shin T, Biorac T, Ryder NS, Goldberg R, Doughty J, He Y. Identification of novel potent bicyclic peptide deformylase inhibitors. Bioorganic & Medicinal Chemistry Letters. 14: 1477-81. PMID 15006385 DOI: 10.1016/J.Bmcl.2004.01.014 |
0.31 |
|
2004 |
He Y, Yang J, Wu B, Risen L, Swayze EE. Synthesis and biological evaluations of novel benzimidazoles as potential antibacterial agents Bioorganic and Medicinal Chemistry Letters. 14: 1217-1220. PMID 14980669 DOI: 10.1016/J.Bmcl.2003.12.051 |
0.322 |
|
2000 |
Nicolaou KC, Jung JK, Yoon WH, He Y, Zhong YL, Baran PS. The Absolute Configuration and Asymmetric Total Synthesis of the CP Molecules (CP-263,114 and CP-225,917, Phomoidrides B and A) We thank Drs. D. H. Huang, G. Siuzdak, and R. Chadha for assistance with NMR spectroscopy, mass spectrometry, and X-ray crystallography, respectively. This work was financially supported by the National Institutes of Health (USA), The Skaggs Institute for Chemical Biology, doctoral fellowships from the National Science Foundation (P.S.B.) and Boehringer Ingelheim (Y.H.), and grants from Array Biopharma, Boehringer Ingelheim, Schering Plough, Pfizer, Glaxo, Merck, Hoffmann-La Roche, DuPont, and Abbott Laboratories. Angewandte Chemie (International Ed. in English). 39: 1829-1832. PMID 10934377 DOI: 10.1002/(Sici)1521-3773(20000515)39:10<1829::Aid-Anie1829>3.0.Co;2-6 |
0.662 |
|
1999 |
Nicolaou KC, Baran PS, Jautelat R, He Y, Fong KC, Choi HS, Yoon WH, Zhong YL. A Novel Route to the Fused Maleic Anhydride Moiety of CP Molecules. Angewandte Chemie (International Ed. in English). 38: 549-552. PMID 29711784 DOI: 10.1002/(Sici)1521-3773(19990215)38:4<549::Aid-Anie549>3.0.Co;2-O |
0.69 |
|
1999 |
Nicolaou KC, Baran PS, Zhong YL, Choi HS, Yoon WH, He Y, Fong KC. Total Synthesis of the CP Molecules CP-263,114 and CP-225,917- Part 1: Synthesis of Key Intermediates and Intelligence Gathering. Angewandte Chemie (International Ed. in English). 38: 1669-1675. PMID 29710978 DOI: 10.1002/(Sici)1521-3773(19990601)38:11<1669::Aid-Anie1669>3.0.Co;2-D |
0.704 |
|
1999 |
Nicolaou KC, Baran PS, Zhong YL, Fong KC, He Y, Yoon WH, Choi HS. Total Synthesis of the CP Molecules CP-225,917 and CP-263,114- Part 2: Evolution of the Final Strategy. Angewandte Chemie (International Ed. in English). 38: 1676-1678. PMID 29710974 DOI: 10.1002/(Sici)1521-3773(19990601)38:11<1676::Aid-Anie1676>3.0.Co;2-T |
0.692 |
|
1999 |
Nicolaou KC, Baran PS, Zhong YL, Choi HS, Fong KC, He Y, Yoon WH. New synthetic technology for the synthesis of hindered alpha-diazoketones via acyl mesylates. Organic Letters. 1: 883-6. PMID 10823217 DOI: 10.1021/Ol990790L |
0.658 |
|
1999 |
Nicolaou KC, He Y, Fong KC, Yoon WH, Choi HS, Zhong YL, Baran PS. Novel strategies to construct the gamma-hydroxy lactone moiety of the CP molecules. Synthesis of the CP-225,917 core skeleton. Organic Letters. 1: 63-6. PMID 10822534 DOI: 10.1021/Ol990551Y |
0.686 |
|
1999 |
Nicolaou KC, King NP, Finlay MR, He Y, Roschangar F, Vourloumis D, Vallberg H, Sarabia F, Ninkovic S, Hepworth D. Total synthesis of epothilone E and related side-chain modified analogues via a Stille coupling based strategy. Bioorganic & Medicinal Chemistry. 7: 665-97. PMID 10400321 DOI: 10.1016/S0968-0896(98)00153-9 |
0.458 |
|
1999 |
Nicolaou KC, Baran PS, Zhong Y, Fong KC, He Y, Yoon WH, Choi H. Totalsynthese der CP-Verbindungen CP-263,114 und CP 225,917 – Teil 2: Entwicklung der Schlußstrategie Angewandte Chemie. 111: 1781-1784. DOI: 10.1002/(Sici)1521-3757(19990601)111:11<1781::Aid-Ange1781>3.0.Co;2-0 |
0.659 |
|
1999 |
Nicolaou KC, Baran PS, Zhong Y, Choi H, Yoon WH, He Y, Fong KC. Totalsynthese der CP-Verbindungen CP-263,114 und CP 225,917 – Teil 1: Synthese von Schlüsselintermediaten und neue präparative Erkenntnisse Angewandte Chemie. 111: 1774-1781. DOI: 10.1002/(Sici)1521-3757(19990601)111:11<1774::Aid-Ange1774>3.0.Co;2-L |
0.677 |
|
1999 |
Nicolaou KC, Baran PS, Jautelat R, He Y, Fong KC, Choi H, Yoon WH, Zhong Y. Ein außergewöhnlicher Zugang zur anellierten Maleinsäureanhydrid-Einheit der CP-Moleküle Angewandte Chemie. 111: 532-535. DOI: 10.1002/(Sici)1521-3757(19990215)111:4<532::Aid-Ange532>3.0.Co;2-Q |
0.658 |
|
1998 |
Nicolaou KC, Finlay MR, Ninkovic S, King NP, He Y, Li T, Sarabia F, Vourloumis D. Synthesis and biological properties of C12,13-cyclopropyl-epothilone A and related epothilones. Chemistry & Biology. 5: 365-72. PMID 9662505 DOI: 10.1016/S1074-5521(98)90070-9 |
0.457 |
|
1998 |
Larock RC, He Y, Leong WW, Han X, Refvik MD, Zenner JM. Palladium-Catalyzed Annulation of Allenes Using Functionally Substituted Vinylic Halides The Journal of Organic Chemistry. 63: 2154-2160. DOI: 10.1021/Jo9717245 |
0.339 |
|
1998 |
Nicolaou KC, He Y, Roschangar F, King NP, Vourloumis D, Li T. Total Synthesis of Epothilone E and Analogues with Modified Side Chains through the Stille Coupling Reaction Angewandte Chemie International Edition. 37: 84-87. DOI: 10.1002/(Sici)1521-3773(19980202)37:1/2<84::Aid-Anie84>3.0.Co;2-V |
0.441 |
|
1998 |
Nicolaou K, He Y, Roschangar F, King N, Vourloumis D, Li T. Totalsynthese von Epothilon E und seitenkettenmodifizierten Epothilon-Analoga durch Stille-Kupplung Angewandte Chemie. 110: 89-92. DOI: 10.1002/(Sici)1521-3757(19980116)110:1/2<89::Aid-Ange89>3.0.Co;2-T |
0.375 |
|
1997 |
Nicolaou KC, Winssinger N, Pastor J, Ninkovic S, Sarabia F, He Y, Vourloumis D, Yang Z, Li T, Giannakakou P, Hamel E. Synthesis of epothilones A and B in solid and solution phase. Nature. 387: 268-72. PMID 9153390 DOI: 10.1038/387268A0 |
0.658 |
|
1997 |
Nicolaou KC, Winssinger N, Pastor J, Ninkovic S, Sarabia F, He Y, Vourloumis D, Yang Z, Li T, Giannakakou P, Hamel E. Correction: Synthesis of epothilones A and B in solid and solution phase Nature. 390: 100-100. DOI: 10.1038/36382 |
0.649 |
|
1997 |
Nicolaou KC, Ninkovic S, Sarabia F, Vourloumis D, He Y, Vallberg H, Finlay MRV, Yang Z. Total syntheses of epothilones A and B via a macrolactonization-based strategy Journal of the American Chemical Society. 119: 7974-7991. DOI: 10.1021/Ja971110H |
0.56 |
|
1997 |
Nicolaou KC, He Y, Vourloumis D, Vallberg H, Roschangar F, Sarabia F, Ninkovic S, Yang Z, Trujillo JI. The olefin metathesis approach to epothilone A and its analogues Journal of the American Chemical Society. 119: 7960-7973. DOI: 10.1021/Ja971109I |
0.513 |
|
1997 |
Nicolaou KC, Sarabia F, Finlay MRV, Ninkovic S, King NP, Vourloumis D, He Y. Total Synthesis of Oxazole‐ and Cyclopropane‐Containing Epothilone B Analogues by the Macrolactonization Approach Chemistry: a European Journal. 3: 1971-1986. DOI: 10.1002/Chem.19970031212 |
0.498 |
|
1997 |
Nicolaou KC, Vallberg H, King NP, Roschangar F, He Y, Vourloumis D, Nicolaou CG. Total Synthesis of Oxazole‐ and Cyclopropane‐Containing Epothilone A Analogues by the Olefin Metathesis Approach Chemistry: a European Journal. 3: 1957-1970. DOI: 10.1002/Chem.19970031211 |
0.514 |
|
1997 |
Nicolaou KC, Vourloumis D, Li T, Pastor J, Winssinger NC, He Y, Ninkovic S, Sarabia F, Vallberg H, Roschangar F, King NP, Finlay MRV, Giannakakou P, Verdier-Pinard P, Hamel E. Designed Epothilones: Combinatorial Synthesis, Tubulin Assembly Properties, abd Cytotoxic Action against Taxol-Resistant Tumor Cells† Angewandte Chemie. 36: 2097-2103. DOI: 10.1002/Anie.199720971 |
0.45 |
|
1997 |
Yang Z, He Y, Vourloumis D, Vallberg H, Nicolaou KC. Total Synthesis of Epothilone A: The Olefin Metathesis Approach Angewandte Chemie. 36: 166-168. DOI: 10.1002/Anie.199701661 |
0.522 |
|
1997 |
Nicolaou KC, Vourloumis D, Li T, Pastor J, Winssinger N, He Y, Ninkovic S, Sarabia F, Vallberg H, Roschanger F, King NP, Finlay MRV, Giannakakou P, Verdier-Pinard P, Hamel E. Gezielt entworfene Epothilone: kombinatorische Synthese, Induktion der Tubulin-Polymerisation und cytotoxische Wirkung gegen taxolresistente Tumorzellen Angewandte Chemie. 109: 2181-2187. DOI: 10.1002/Ange.19971091917 |
0.609 |
|
1997 |
Yang Z, He Y, Vourloumis D, Vallberg H, Nicolaou KC. Die Totalsynthese Von Epothilon A : Der Zugang Durch Olefinmetathese Angewandte Chemie. 109: 170-172. DOI: 10.1002/Ange.19971090157 |
0.443 |
|
1996 |
Nicolaou KC, He Y, Vourloumis D, Vallberg H, Yang Z. An Approach to Epothilones Based on Olefin Metathesis Angewandte Chemie. 35: 2399-2401. DOI: 10.1002/Anie.199623991 |
0.459 |
|
1996 |
Nicolaou KC, He Y, Vourloumis D, Vallberg H, Yang Z. Durch Olefinmetathese zum Epothilongerüst Angewandte Chemie. 108: 2554-2556. DOI: 10.1002/Ange.19961082032 |
0.436 |
|
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