Toward Bicalutamide Analogues with High Structural Diversity Using Catalytic Asymmetric Oxohydroxylation-Reference-Cited by-同舟云学术

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Toward Bicalutamide Analogues with High Structural Diversity Using Catalytic Asymmetric Oxohydroxylation

Published:2024-03-01 Issue:6 Volume:89 Page:3907-3911
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Chen Xinrui¹,Tian Jinxin¹,Wang Shuangshuang²,Wang Chao²^ORCID,Zong Lili¹^ORCID

Affiliation:

1. Fujian Provincial Key Laboratory of Innovative Drug Target Research, School of Pharmaceutical Sciences, Xiamen University, Xiamen 361102, China

2. Institute of Advanced Synthesis, School of Chemistry and Molecular Engineering, Nanjing Tech University, Nanjing 211816, China

Funder

Ministry of Human Resources and Social Security

National Natural Science Foundation of China

Xiamen University

Publisher

American Chemical Society (ACS)

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.joc.3c02735

Reference35 articles.

1. Bicalutamide (Casodex®) in the treatment of prostate cancer

2. Worldwide activity and safety of bicalutamide: a summary review

3. Therapeutic Strategies to Target the Androgen Receptor

4. Enantioselective binding of Casodex to the androgen receptor

5. Chiral Nonsteroidal Affinity Ligands for the Androgen Receptor. 1. Bicalutamide Analogues Bearing Electrophilic Groups in the B Aromatic Ring

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