| scholarly article | Q13442814 |
| P356 | DOI | 10.1002/1521-3773(20020415)41:8<1381::AID-ANIE1381>3.0.CO;2-O |
| P698 | PubMed publication ID | 19750771 |
| P2093 | author name string | Jian Sun | |
| Subhash C Sinha | |||
| P2860 | cites work | Concise total syntheses of epothilone A and C based on alkyne metathesis | Q57945480 |
| Epothilone A and B—Novel 16-Membered Macrolides with Cytotoxic Activity: Isolation, Crystal Structure, and Conformation in Solution | Q60357921 | ||
| Total Synthesis of Epothilone A: The Olefin Metathesis Approach | Q60357925 | ||
| Total Synthesis of(−)-Epothilone A | Q60357927 | ||
| Total synthesis of epothilones B and D | Q74146417 | ||
| Synthesis and biological activity of novel epothilone aziridines | Q74378229 | ||
| Studies toward a Synthesis of Epothilone A: Stereocontrolled Assembly of the Acyl Region and Models for Macrocyclization | Q74824762 | ||
| Total synthesis of epothilone B | Q77143289 | ||
| Chemical Biology of Epothilones | Q88519454 | ||
| Stereoselective syntheses of epothilones A and B via directed nitrile oxide cycloaddition | Q28208674 | ||
| Synthesis and Applications of RuCl2(CHR‘)(PR3)2: The Influence of the Alkylidene Moiety on Metathesis Activity | Q30040302 | ||
| Synthesis and activity of a new generation of ruthenium-based olefin metathesis catalysts coordinated with 1,3-dimesityl-4,5-dihydroimidazol-2-ylidene ligands | Q30596579 | ||
| Synthesis of natural-product-based compound libraries | Q30873370 | ||
| Microtubule-stabilizing agents: a growing class of important anticancer drugs | Q34318072 | ||
| Recent developments in the chemistry, biology and medicine of the epothilones | Q34870258 | ||
| The synthesis, discovery, and development of a highly promising class of microtubule stabilization agents: curative effects of desoxyepothilones B and F against human tumor xenografts in nude mice | Q36541279 | ||
| The antibody catalysis route to the total synthesis of epothilones | Q36752669 | ||
| Antitumor efficacy of 26-fluoroepothilone B against human prostate cancer xenografts | Q40768370 | ||
| Chemical synthesis and biological evaluation of cis- and trans-12,13-cyclopropyl and 12,13-cyclobutyl epothilones and related pyridine side chain analogues. | Q40779922 | ||
| Total synthesis of epothilone B, epothilone D, and cis- and trans-9,10-dehydroepothilone D. | Q40801585 | ||
| Synthesis of trisubstituted alkenes via olefin cross-metathesis | Q41738988 | ||
| Catalytic antibody route to the naturally occurring epothilones: total synthesis of epothilones A-F. | Q43605353 | ||
| The 12,13-diol cyclization approach for a truly stereocontrolled total synthesis of epothilone B and the synthesis of a conformationally restrained analogue | Q43644646 | ||
| Synthesis of epothilone analogues by antibody-catalyzed resolution of thiazole aldol synthons on a multigram scale. Biological consequences of C-13 alkylation of epothilones | Q43877268 | ||
| New insights into the mechanism of ruthenium-catalyzed olefin metathesis reactions | Q46092178 | ||
| Mechanism and activity of ruthenium olefin metathesis catalysts | Q46357398 | ||
| Total synthesis of 16-desmethylepothilone B, epothilone B10, epothilone F, and related side chain modified epothilone B analogues | Q46483091 | ||
| Insights into long-range structural effects on the stereochemistry of aldol condensations: a practical total synthesis of desoxyepothilone F. | Q49328538 | ||
| Activities of the microtubule-stabilizing agents epothilones A and B with purified tubulin and in cells resistant to paclitaxel (Taxol(R)). | Q52196656 | ||
| Epothilon A und B – neuartige, 16gliedrige Makrolide mit cytotoxischer Wirkung: Isolierung, Struktur im Kristall und Konformation in Lösung | Q56681180 | ||
| P433 | issue | 8 | |
| P921 | main subject | stereoselectivity | Q903429 |
| P304 | page(s) | 1381-1383 | |
| P577 | publication date | 2002-04-01 | |
| P1433 | published in | Angewandte Chemie | Q538683 |
| P1476 | title | Stereoselective total synthesis of epothilones by the metathesis approach involving C9-C10 bond formation | |
| P478 | volume | 41 |
| Q35683577 | 4. The natural products epothilones A and B as lead structures for anticancer drug discovery: chemistry, biology, and SAR studies |
| Q36752835 | The chemistry and biology of epothilones--the wheel keeps turning. |
| Q83329353 | Total synthesis of epothilones A-F |
| Q37329400 | Total synthesis of epothilones B and D: stannane equivalents for beta-keto ester dianions |
Search more.