One pot stereoselective synthesis of chiral α,ω-diynes from bromoallenes and organobis(heterocuprates)

Organobis(heterocuprates), 7 and 8, have been prepared reacting in situ 1,4-dilithiobutane and di-Grignard reagents, obtained from 1,4-dibromobutane and 1,4-dibromobenzene, respectively, with CuSPh and LiCuBr2. The cross-coupling reaction of these di-cuprate reagents with 3-alkyl and 3,3-dialkyl 1-bromo-1,2-dienes (1) provides a general method for selective synthesis of 1,9-decadiynes (5) and 1,4-bis(2-propynyl)benzenes (6), characterized by two identical chiral centres in the alfa position to the triple bonds. The high 1,3-anti stereoselectivity of the coupling process allows us to obtain enantiomerically enriched alfa-omega-diynes 5 and 6 starting from optically active allenic substrates