The　transition-metal-catalyzed　allylation　reaction　is　an　efficient　strategy　for　the　construction　of　new　carbon-carbon　bonds　alongside　allyl　or　homoallylic　functionalization.　Herein　we　describe　a　Ni-catalyzed　reductive　allylation　of　alpha-chloroboronates　to　efficiently　render　the　corresponding　homoallylic　boronates,　which　could　be　readily　converted　into　valuable　homoallylic　alcohols　or　amines　or　1,4-diboronates.　This　reaction　features　a　broad　substrate　scope　with　good　functional　group　compatibility　that　is　complementary　to　the　existing　methods　for　the　preparation　of　homoallylic　boronates.