Enantioselective Synthesis of Spiroindolines via Cascade Isomerization/Spirocyclization/Dearomatization Reaction

التفاصيل البيبلوغرافية
العنوان: Enantioselective Synthesis of Spiroindolines via Cascade Isomerization/Spirocyclization/Dearomatization Reaction
المؤلفون: Wenbin Shang, Xu Ji, Yuchang Liu, Chengfeng Xia, Zhiqiang Pan, Qinglong Liu, Fengchi Hu
المصدر: Organic Letters. 22:1589-1593
بيانات النشر: American Chemical Society (ACS), 2020.
سنة النشر: 2020
مصطلحات موضوعية: Indole test, 010405 organic chemistry, Monoterpene, Organic Chemistry, Enantioselective synthesis, 010402 general chemistry, 01 natural sciences, Biochemistry, Combinatorial chemistry, 0104 chemical sciences, Catalysis, Enamine, chemistry.chemical_compound, Cascade reaction, chemistry, Physical and Theoretical Chemistry, Nonane, Isomerization
الوصف: The spiroindoline skeleton featured with 2,7-diazaspiro[4.4]nonane exists in various structurally intricate and biologically active monoterpene indole alkaloids. A catalytic asymmetric cascade enamine isomerization/spirocyclization/dearomatization succession to construct the spiroindoline was developed, which employed the indolyl dihydropyridine as a substrate under catalysis of the chiral phosphoric acid. This cascade reaction provided various spiroindolines in both diastereoselective and enantionselective fashions.
تدمد: 1523-7052
1523-7060
DOI: 10.1021/acs.orglett.0c00181
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::be9623cb2073c63d12da49794becb4ae
https://doi.org/10.1021/acs.orglett.0c00181
Rights: CLOSED
رقم الانضمام: edsair.doi.dedup.....be9623cb2073c63d12da49794becb4ae
قاعدة البيانات: OpenAIRE
الوصف
تدمد:15237052
15237060
DOI:10.1021/acs.orglett.0c00181