Tetrahedron Letters p. 773 - 776 (1993)
Update date:2022-08-17
Topics:
Lautens, Mark
Chiu, Pauline
The ring opening of unsymmetrical oxabicyclic compounds was found to be highly regioselective, giving rise to products from the attack of the nucleophile distal to the bridgehead substituent. Ozonolysis furnished acyclic chains with up to five stereocenters and differentiated ends.
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