TY - JOUR
T1 - Synthesis and Diels-Alder reactions of allylidenecyclopropane [4]
AU - Zutterman, F.
AU - Krief, A.
PY - 1983/1/1
Y1 - 1983/1/1
N2 - Allylidenecyclopropane, readily available from 1-lithio-1-(phenylthio)cyclopropane, reacts with a large variety of electrophilic olefins and produces functionalized spirooctenes. The reactions are, in most cases, highly regioselective but lead mainly to the unexpected regioisomers.
AB - Allylidenecyclopropane, readily available from 1-lithio-1-(phenylthio)cyclopropane, reacts with a large variety of electrophilic olefins and produces functionalized spirooctenes. The reactions are, in most cases, highly regioselective but lead mainly to the unexpected regioisomers.
UR - http://www.scopus.com/inward/record.url?scp=0002315059&partnerID=8YFLogxK
M3 - Article
AN - SCOPUS:0002315059
SN - 0022-3263
VL - 48
SP - 1135
EP - 1137
JO - Journal of Organic Chemistry
JF - Journal of Organic Chemistry
IS - 7
ER -