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1.
J Org Chem ; 63(17): 5831-5837, 1998 Aug 21.
Article in English | MEDLINE | ID: mdl-11672184

ABSTRACT

We achieved a total synthesis of terprenin, a novel potent immunoglobulin E antibody suppressant which was obtained from the fermentation broth of Aspergillus candidus RF-5672 and has a highly oxygenated p-terphenyl skeleton with a prenyloxy side chain. The key steps relied on the Suzuki reaction to construct the terphenyl skeleton and on regioselective halogenations to selectively combine the aromatic rings. The highly efficient and practical production of this important natural product offers promise for the development of a new type of antiallergic drug.

2.
Angew Chem Int Ed Engl ; 37(7): 973-975, 1998 Apr 20.
Article in English | MEDLINE | ID: mdl-29711491

ABSTRACT

Regioselective halogenations and Suzuki reactions ensure proper linkage of the aromatic rings in two total syntheses of terprenin (1). Both routes make it possible to prepare 1 efficiently and in large quantity.

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