183614-26-8Relevant articles and documents
Stereoselective preparation of highly functionalized (Z)-3-copper enoates by an iodine-copper exchange reaction
Yang, Xiaoyin,Knochel, Paul
, p. 2167 - 2172 (2006)
3-Iodoenoates are readily converted into the corresponding alkenylcopper species with complete retention of configuration of the double bond via an iodine-copper exchange reaction. Quenching reactions with various electrophiles provide highly functionalized enoates in good yields. Georg Thieme Verlag Stuttgart.