4.8 Article

N-methoxy-N-acylnitrenium ions:: Application to the formal synthesis of (-)-TAN1251A

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卷 3, 期 7, 页码 1053-1056

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AMER CHEMICAL SOC
DOI: 10.1021/ol015626o

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  1. NIGMS NIH HHS [GM59157-01] Funding Source: Medline

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[GRAPHICS] A formal synthesis of the muscarinic M-1 receptor antagonist (-)-TAN1251A (7) from L-tyrosine is described. Central to this venture has been the construction of the 1-azaspiro[4.5]decane skeleton present in the natural product by an N-methoxy-N-acylnitrenium ion-induced spirocyclization. The dienone generated in this transformation, 10, was converted to (-)-TAN1251A via tricycle 9, an intermediate in Kawahara's recent synthesis of racemic 7.

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