The intramolecular nitrile oxide cycloaddition route to spirocyclic alkaloids. A total synthesis of isonitramine and sibirine

Alan P. Kozikowski; P. W. Yuen

doi:10.1039/c39850000847

The intramolecular nitrile oxide cycloaddition route to spirocyclic alkaloids. A total synthesis of isonitramine and sibirine

Alan P. Kozikowski, P. W. Yuen

Research output: Contribution to journal › Article › peer-review

27 Scopus citations

Abstract

The intramolecular nitrile oxide cycloaddition reaction has been found to accommodate the construction of spirocycles in modest yield as revealed by a synthesis of the title alkaloids.

Original language	English (US)
Pages (from-to)	847-848
Number of pages	2
Journal	Journal of the Chemical Society, Chemical Communications
Issue number	13
DOIs	https://doi.org/10.1039/c39850000847
State	Published - 1985
Externally published	Yes

ASJC Scopus subject areas

Molecular Medicine

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title = "The intramolecular nitrile oxide cycloaddition route to spirocyclic alkaloids. A total synthesis of isonitramine and sibirine",

abstract = "The intramolecular nitrile oxide cycloaddition reaction has been found to accommodate the construction of spirocycles in modest yield as revealed by a synthesis of the title alkaloids.",

author = "Kozikowski, {Alan P.} and Yuen, {P. W.}",

year = "1985",

doi = "10.1039/c39850000847",

language = "English (US)",

pages = "847--848",

journal = "Journal of the Chemical Society, Chemical Communications",

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publisher = "Royal Society of Chemistry",

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AU - Kozikowski, Alan P.

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PY - 1985

Y1 - 1985

N2 - The intramolecular nitrile oxide cycloaddition reaction has been found to accommodate the construction of spirocycles in modest yield as revealed by a synthesis of the title alkaloids.

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M3 - Article

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JO - Journal of the Chemical Society, Chemical Communications

JF - Journal of the Chemical Society, Chemical Communications

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ER -

The intramolecular nitrile oxide cycloaddition route to spirocyclic alkaloids. A total synthesis of isonitramine and sibirine

Abstract

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