“…209 Also monochlorocyclopropanes give the same process. 210,211 The same process with 1-methyl-2-chlorocyclopropane 154 in the presence of a crown ether has led to the formation of cyclopropylmethylenecyclopropane 155 in good yields (Scheme 50). 212 When the elimination is carried out in the presence of a nucleophile (alcohol, thiol, or amine) the formation of the methylenecyclopropane is accompanied by nucleophilic substitution.…”
Section: Eliminations Of Hx Groups (X ) Halides)mentioning
confidence: 99%
“…When n = 1 the primary endo -methylenecyclopropane rearranges to the exo -methylenecyclopropane 153 with ring contraction (Scheme ) , …”
“…209 Also monochlorocyclopropanes give the same process. 210,211 The same process with 1-methyl-2-chlorocyclopropane 154 in the presence of a crown ether has led to the formation of cyclopropylmethylenecyclopropane 155 in good yields (Scheme 50). 212 When the elimination is carried out in the presence of a nucleophile (alcohol, thiol, or amine) the formation of the methylenecyclopropane is accompanied by nucleophilic substitution.…”
Section: Eliminations Of Hx Groups (X ) Halides)mentioning
confidence: 99%
“…When n = 1 the primary endo -methylenecyclopropane rearranges to the exo -methylenecyclopropane 153 with ring contraction (Scheme ) , …”
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