Iron-Catalyzed Enantioselective Radical Carboazidation and Diazidation of α,β-Unsaturated Carbonyl Compounds

التفاصيل البيبلوغرافية
العنوان: Iron-Catalyzed Enantioselective Radical Carboazidation and Diazidation of α,β-Unsaturated Carbonyl Compounds
المؤلفون: Yun-Dong Wu, Shunxi Dong, Maoping Pu, Jun He, Wen Liu, Tinghui Zhang, Xiaoming Feng, Xiaohua Liu
المصدر: Journal of the American Chemical Society. 143:11856-11863
بيانات النشر: American Chemical Society (ACS), 2021.
سنة النشر: 2021
مصطلحات موضوعية: Chemistry, Iron catalyzed, Radical, Enantioselective synthesis, chemistry.chemical_element, General Chemistry, Biochemistry, Nitrogen, Medicinal chemistry, Catalysis, chemistry.chemical_compound, Colloid and Surface Chemistry, Intramolecular force, Organic synthesis, Vicinal
الوصف: Azidation of alkenes is an efficient protocol to synthesize organic azides which are important structural motifs in organic synthesis. Enantioselective radical azidation, as a useful strategy to install a C-N3 bond, remains challenging due to the inherently instability and unique structure of radicals. Here, we disclose an efficient enantioselective radical carboazidation and diazidation of α,β-unsaturated ketones and amides catalyzed by chiral N,N'-dioxide/Fe(OTf)2 complexes. An array of substituted alkenes was transformed to the corresponding α-azido carbonyl derivatives in good to excellent enantioselectivities, benefiting the preparation of chiral α-amino ketones, vicinal amino alcohols, and vicinal diamines. Control experiments and mechanistic studies proved the radical pathway in the reaction process. The DFT calculations showed that the azido transferred to the radical intermediate via an intramolecular five-membered transition state with the internal nitrogen of the Fe-N3 species.
تدمد: 1520-5126
0002-7863
DOI: 10.1021/jacs.1c05881
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aa5a0801d7ba8a2b300077f4678cef71
https://doi.org/10.1021/jacs.1c05881
Rights: CLOSED
رقم الانضمام: edsair.doi.dedup.....aa5a0801d7ba8a2b300077f4678cef71
قاعدة البيانات: OpenAIRE
الوصف
تدمد:15205126
00027863
DOI:10.1021/jacs.1c05881