Journal of Organic Chemistry p. 1985 - 1987 (1986)
Update date:2022-07-30
Topics: Regioselectivity Yield NMR spectroscopy Nucleophile Rearrangement TLC (thin-layer chromatography) Aryl group Azidation Halogenation Solvent Effects Stereoselectivity Anti-Markovnikov Addition Regiochemistry Radical mechanism Electrophilic addition Polar Mechanism
Sivasubramanian, Shanmugaperumal
Aravind, Sivasubramanian
Kumarasingh, Lovejoy Theodore
Arumugam, Natesan
The addition products of iodine azide to several 1-arylcyclohexanes have been shown to be 2-azido-1-iodo-1-arylcyclohexanes and not 1-azido-2-iodo-1-arylcyclohexanes as reported by Hassner et al.
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Doi:10.1002/hlca.200900149
(2009)Doi:10.1021/acs.orglett.1c00085
(2021)Doi:10.1007/BF00771640
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(2009)Doi:10.1039/c39880001030
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