The various approaches which have been used to prepare macromonomers a
re presented in the first part of this review. Besides the pathways' b
ased on ''living'' polymerizations, intense efforts have been devoted
to develop methods allowing access to macromonomers by transformation
of omega-functional polymers. In the second part of this survey, the a
bility of macromonomers to copolymerize with comonomers and to homopol
ymerize is discussed. It appears that the macromonomers generally exhi
bit a lower reactivity than their micromolecular models. The reasons f
or this behaviour are commented upon.