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Cited by 164

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Total Synthesis of (–)‐Epothilone B: An Extension of the Suzuki Coupling Method and Insights into Structure–Activity Relationships of the Epothilones

Su, Dai‐Shi, Meng, Dongfang, Bertinato, Peter, Balog, Aaron, Sorensen, Erik J., Danishefsky, Samuel J., Zheng, Yu‐Huang, Chou, Ting‐Chao, He, Lifeng, Horwitz, Susan B.·1997·Angewandte Chemie International Edition in English

Abstract

The highest biological activities displayed by epothilone-related compounds have been found for epothilone B (1) and a derivative that was prepared en route to the natural product. Key steps in the total synthesis were a Suzuki coupling providing a trisubstituted double bond in the macrocycle and its subsequent stereoselective epoxidation with dimethyldioxirane.

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Authors
Su, D., Meng, D., Bertinato, P., Balog, A., Sorensen, E. J., Danishefsky, S. J., Zheng, Y., Chou, T., He, L., & Horwitz, S. B.
Venue
Angewandte Chemie International Edition in English
Publisher
Wiley
Published
1997-04-18
Volume
36
Issue
7
Pages
757-759
ISSN
0570-0833 (ISSN-L)
OpenAlex
W2069635625
Cited by
164
References
0
FWCI
19.48
Type
journal article
Language
en
Open access
closed

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CoChat. (2026). Citation check: Total Synthesis of (–)‐Epothilone B: An Extension of the Suzuki Coupling Method and Insights into Structure–Activity Relationships of the Epothilones. https://app.cochat.ai/papers/10.1002/anie.199707571
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Su, D., Meng, D., Bertinato, P., Balog, A., Sorensen, E. J., Danishefsky, S. J., Zheng, Y., Chou, T., He, L., & Horwitz, S. B. (1997). Total Synthesis of (–)‐Epothilone B: An Extension of the Suzuki Coupling Method and Insights into Structure–Activity Relationships of the Epothilones. Angewandte Chemie International Edition in English. https://doi.org/10.1002/anie.199707571

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.