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Enantiose
lective copper-cata
lyzed a
lly
lic a
lky
lations were performed on a
lly
lic bromides with a protectedhydroxy
l or amine functiona
l group using severa
l Grignard reagents and Taniaphos
L1 as a
ligand. Thetermina
l o
lefin moiety in the products was transformed into various functiona
l groups without racemization,providing faci
le access to a variety of versati
le bifunctiona
l chira
l bui
lding b
locks.