Catalytic Asymmetric Total Synthesis of Leucinostatin A

التفاصيل البيبلوغرافية
العنوان: Catalytic Asymmetric Total Synthesis of Leucinostatin A
المؤلفون: Takumi Watanabe, Masakatsu Shibasaki, Hikaru Abe
المصدر: The Chemical Record. 21:175-187
بيانات النشر: Wiley, 2020.
سنة النشر: 2020
مصطلحات موضوعية: 010405 organic chemistry, Stereochemistry, Chemistry, General Chemical Engineering, Absolute configuration, Total synthesis, Antineoplastic Agents, Stereoisomerism, General Chemistry, 010402 general chemistry, 01 natural sciences, Biochemistry, Catalysis, 0104 chemical sciences, Residue (chemistry), Cell Line, Tumor, Materials Chemistry, Side chain, Humans, Structure–activity relationship, Stereoselectivity, Leucinostatin, Antimicrobial Cationic Peptides
الوصف: This review describes our efforts toward achieving catalytic asymmetric total synthesis of leucinostatin A, a compound that interferes with the tumor-stroma interaction. The synthesis utilizes four catalytic asymmetric reactions, including direct-type reactions exemplified by high atom-economy, and three C-C bond forming reactions. Thorough analysis of the NMR data, HPLC profiles, and biologic activity led us to unambiguously revise the absolute configuration regarding the 6-position of the AHMOD residue side chain from S (reported) to R. Other examples of previously reported important studies on the stereoselective synthesis of HyLeu and AHMOD are also described.
تدمد: 1528-0691
1527-8999
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f1f0b176abb8ec40aff0185c7a8e1374
https://doi.org/10.1002/tcr.202000108
حقوق: CLOSED
رقم الأكسشن: edsair.doi.dedup.....f1f0b176abb8ec40aff0185c7a8e1374
قاعدة البيانات: OpenAIRE