Synthesis of Tamibarotene via Ullmann-Type Coupling
Author:
Affiliation:
1. Key Laboratory of Structure-Based Drug Design & Discovery, Ministry of Education, Shenyang Pharmaceutical University, Shenyang 110016, China
Funder
Natural Science Foundation of Liaoning Province
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Physical and Theoretical Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.oprd.7b00089
Reference39 articles.
1. Thomson reuters, integrity [EB/OL]https://integrity.thomson-pharma.com/integrity/xmlxsl/pk_prod_list.exec_form_pro_pr?p_par_pro=PRO_DRUG_NAME&p_val_pro=Tamibarotene&p_origen=PROD&p_oper_pro=AND&p_par_tar=&p_val_tar=&p_oper_tar=AND&p_par_ref=&p_val_ref=&p_oper_ref=AND&p_par_pat=&p_val_pat=&p_oper_pat=AND#1, Jan 18, 2017.
2. aNational Institutes of Health [EB/OL] https://clinicaltrials.gov/ct2/results?term=Tamibarotene&Search=Search, Jan 18, 2017.
3. Tamibarotene in patients with acute promyelocytic leukaemia relapsing after treatment with all-transretinoic acid and arsenic trioxide
4. Cooperative Therapeutic Action of Retinoic Acid Receptor and Retinoid X Receptor Agonists in a Mouse Model of Alzheimer's Disease
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