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[摘要]：The prepn. of tricyclic amines from acyclic precursors is described using a cascade of tandem reactions involving condensation of an aldehyde with a primary amine, cyclization (with displacement of a halide), and then in situ deprotonation or decarboxylation to give an azomethine ylide or nitrone followed by intramol. dipolar cycloaddn. The methodol. is straightforward, and the aldehyde precursors are prepd. easily and quickly in high yield using nitrile alkylations followed by DIBAL-H redn. The relative ease of reaction of various substrates with different tether lengths between the aldehyde and the halide or dipolarophile has been studied. Several primary amines including simple amino acids such as glycine, alanine, and phenylalanine and derivs. such as glycine Et ester and also hydroxylamine have been investigated. High yields are obtained in the formation of different tricyclic ring sizes; the dipolar cycloaddn. necessarily creates a five-membered ring, and we have investigated the formation of five- and six-membered rings for the other two new ring sizes. In all cases, yields are high (except when using glycine when the tether to the terminal alkene dipolarophile leads to a six-membered ring), and most efficient is the formation of the tricyclic product in which all five-membered rings are formed. Examples with an alkyne as the dipolarophile were also successful. In all the reactions studied, the products are formed with complete regioselectivity and remarkably with complete stereoselectivity. The key step involves the formation of three new rings and potentially up to four new stereocenters in a single transformation. The power of the chem. was demonstrated by the synthesis of the core ring systems of the alkaloids (?-scandine and (?-myrioneurinol and the total syntheses of the alkaloids (?-aspidospermine (I), (?-quebrachamine (II), and (?-aspidospermidine (III). |
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