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Angew Chem Int Ed Engl ; 48(27): 5022-5, 2009.
Article in English | MEDLINE | ID: mdl-19496091

ABSTRACT

Caught in the middle: The ionomycin calcium complex (see structure; O red, Ca green) was the target of an approach featuring the efficient asymmetric synthesis of an allene by a copper(I)-mediated anti-selective S(N)2' reaction, a highly stereoselective gold(III)-catalyzed cycloisomerization of an alpha-hydroxyallene, and a Rh-catalyzed rearrangement of an alpha-diazo-beta-hydroxyketone.


Subject(s)
Calcium/chemistry , Ionomycin/chemistry , Anti-Bacterial Agents/chemistry , Catalysis , Cyclization , Gold/chemistry , Stereoisomerism
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