1361964-70-6Relevant academic research and scientific papers
Regioselective (Diacetoxyiodo)benzene-promoted halocyclization of unfunctionalized olefins
Liu, Gong-Qing,Li, Yue-Ming
, p. 10094 - 10109 (2014)
A metal-free method for intramolecular halocyclization of unfunctionalized olefins was detailed. (Diacetoxyiodo)benzene (PIDA) was very effective for haloamidation, haloetherification, and halolactonization of unfunctionalized olefins. In the presence of
MnI2-catalyzed regioselective intramolecular iodoamination of unfunctionalized olefins
Sun, Hui,Cui, Bin,Liu, Gong-Qing,Li, Yue-Ming
supporting information, p. 7170 - 7178 (2016/10/24)
MnI2-catalyzed intramolecular iodoamination of unfunctionalized olefins was reported. Interaction of MnI2with N-alkenyl amine/sulfonamide gave [sbnd]NRMnI which produced a [sbnd]CH2MnI intermediate via intramolecular amino
Highly selective palladium-catalyzed intramolecular chloroamination of unactivated alkenes by using hydrogen peroxide as an oxidant
Yin, Guoyin,Wu, Tao,Liu, Guosheng
supporting information; experimental part, p. 451 - 455 (2012/02/15)
Cheap and clean! A novel Pd-catalyzed oxidative intramolecular chloroamination of unactivated alkenes has been developed by using hydrogen peroxide as an oxidant and CaCl2 as a chlorine source. A series of chlorinated piperidine derivatives has
