30186-48-2Relevant articles and documents
5(6)-anti-substituted-2-azabicyclo[2.1.1]hexanes: A nucleophilic displacement route
Krow, Grant R.,Edupuganti, Ram,Gandla, Deepa,Choudhary, Amit,Lin, Guoliang,Sonnet, Philip E.,DeBrosse, Charles,Ross III, Charles W.,Cannon, Kevin C.,Raines, Ronald T.
, p. 8232 - 8242 (2009)
(Chemical Equation Presented) Nucleophilic displacements of 5(6)-anti-bromo substituents in 2-azabicyclo[2.1.1]hexanes (methanopyrrolidines) have been accomplished. These displacements have produced 5-anti-X-6-anti-Y- difunctionalized-2-azabicyclo[2.1.1]h
Photocatalyst-controlled and visible light-enabled selective oxidation of pyridinium salts
Peng, Xiang-Jun,He, Hai-Ping,Liu, Qian,She, Kun,Zhang, Bao-Qi,Wang, Heng-Shan,Tang, Hai-Tao,Pan, Ying-Ming
, p. 753 - 760 (2021/03/31)
This study proposes two different methods of photocatalytic-controlled and visible light-induced selective oxidation of pyridiniums with air as the terminal oxidant. The key to these transformations is to choose the appropriate light source and photocatal
3-formylpyrroles from 3-furfurylamines by bromine oxidation reaction
Harn, Piin-Jye,Lin, Chu-Chung,Wu, Hsien-Jen
, p. 1321 - 1326 (2011/10/07)
Oxidation of 3-furfurylamines 3a-e with bromine in acetone-water solution gave N-substituted 3-formylpyrroles 4a-e in good yields. A reaction mechanism via the Clauson-Kaas reaction followed by the cis-trans isomerization of the 2-ene-1,4-diones 13 and 14
