34495-73-3Relevant articles and documents
TOTAL STEREOSPECIFICITY IN FREE RADICAL INTRAMOLECULAR ADDITION: CYCLISATION OF CIS AND TRANS 1-METHYL 4-HEXENYL N-CHLOROAMINES BY MEANS OF METALLIC SALTS
Bougeois, Jean-Luc,Stella, Lucien,Surzur, Jean-Marie
, p. 61 - 64 (1981)
Extremely high stereospecificity (up to 100percent diastereoisomeric purity) can be obtained for the metallic salts induced radical cyclisation of the cis and trans 1-methyl 4-hexenyl N-chloroamines.A possible mechanism for the highly effective trans-addition using metal-complexed aminyl radical is proposed.
REACTIONS OF ORGANIC HALIDES WITH OLEFINS UNDER Ni0-CATALYSIS. FORMAL ADDITION OF HYDROCARBONS TO CC-DOUBLE BONDS
Sustmann, Reiner,Hopp, Peter,Holl, Peter
, p. 689 - 692 (2007/10/02)
The reaction of various types of organic halides with electron deficient olefins under the influence of NiCl2 x 6 H2O in the presence of zinc and pyridine leads to formal addition products of hydrocarbons to CC-double bonds in good yield.