75586-32-2Relevant articles and documents
Catalytic Diazosulfonylation of Enynals toward Diazoindenes via Oxidative Radical-Triggered 5-exo-trig Carbocyclizations
Hao, Wen-Juan,Du, Yan,Wang, Dan,Jiang, Bo,Gao, Qian,Tu, Shu-Jiang,Li, Guigen
, p. 1884 - 1887 (2016)
Catalytic diazosulfonylation of enynals with arylsulfonyl hydrazides has been established by using tert-butyl hydroperoxide (TBHP) as the oxidant with tetrabutylammonium iodide (TBAI) under a convenient system. The reaction occurred through oxidative radical-triggered 5-exo-trig carbocyclization cascading to afford sulfonylated diazoindenes regioselectively. The new diazosulfonylation reaction features a broad substrate scope, readily accessible starting materials, and a simple one-pot process.
HETEROCYCLIC COMPOUND AND ORGANIC LIGHT EMITTING DEVICE COMPRISING SAME
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Paragraph 0136; 0138; 0143, (2020/11/24)
The present specification relates to a heterocyclic compound represented by Chemical Formula 1, and an organic light emitting device comprising the same.
Pyrazoloisoquinoline compound and synthesis method thereof
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Paragraph 0038; 0041; 0042, (2016/10/07)
The invention discloses a pyrazoleoisoquinoline compound and a synthesis method thereof. The pyrazoleoisoquinoline compound is represented by a formula I, wherein the R1 represents hydrogen, halogen atoms and alkyl or alkoxy or amino, and the R2 represents hydrogen, halogen atoms and alkyl or alkoxy or amino. The target product is synthesized through four-step reaction, the synthesis method is simple and rapid, the target compound is higher in yield, and a necessary foundation is provided for further research on the compound represented by the formula I or related compounds. In addition, the intermediate provided in the synthesis method is simple in structure and easy to obtain and provides convenience for the preparation of the target compound.