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Two stereocontrolled palladium-catalyzed cross-couplings of I-alkenyl
boronic acids and aryl/alkenyl halides (the Suzuki-Miyaura reaction) a
re the key steps in an enantioselective approach to the polyene fragme
nt of haminols A and B, alarm pheromones isolated from Haminoea navicu
la, a Cephalaspidean Opisthobranch mollusc. Chirality rested on the us
e of (S)-propylene oxide as the starting material. (C) 1998 Elsevier S
cience Ltd. All rights reserved.