Generation of N-acyliminium ions via intramolecular conjugate addition reactions: A strategy for the total synthesis of nakadomarin A

Mark G. Nilson; Raymond L. Funk

doi:10.1021/ol061463y

Generation of N-acyliminium ions via intramolecular conjugate addition reactions: A strategy for the total synthesis of nakadomarin A

Mark G. Nilson, Raymond L. Funk

Chemistry

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

39 Scopus citations

Abstract

The rapid construction of the tetracyclic core ring system of nakadomarin A via a tandem enecarbamate Michael addition/N-acyliminium ion cyclization is described.

Original language	English (US)
Pages (from-to)	3833-3836
Number of pages	4
Journal	Organic Letters
Volume	8
Issue number	17
DOIs	https://doi.org/10.1021/ol061463y
State	Published - Aug 17 2006

All Science Journal Classification (ASJC) codes

Biochemistry
Physical and Theoretical Chemistry
Organic Chemistry

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10.1021/ol061463y

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title = "Generation of N-acyliminium ions via intramolecular conjugate addition reactions: A strategy for the total synthesis of nakadomarin A",

abstract = "The rapid construction of the tetracyclic core ring system of nakadomarin A via a tandem enecarbamate Michael addition/N-acyliminium ion cyclization is described.",

author = "Nilson, {Mark G.} and Funk, {Raymond L.}",

year = "2006",

month = aug,

day = "17",

doi = "10.1021/ol061463y",

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volume = "8",

pages = "3833--3836",

journal = "Organic Letters",

issn = "1523-7060",

publisher = "American Chemical Society",

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T1 - Generation of N-acyliminium ions via intramolecular conjugate addition reactions

T2 - A strategy for the total synthesis of nakadomarin A

AU - Nilson, Mark G.

AU - Funk, Raymond L.

PY - 2006/8/17

Y1 - 2006/8/17

N2 - The rapid construction of the tetracyclic core ring system of nakadomarin A via a tandem enecarbamate Michael addition/N-acyliminium ion cyclization is described.

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JO - Organic Letters

JF - Organic Letters

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Generation of N-acyliminium ions via intramolecular conjugate addition reactions: A strategy for the total synthesis of nakadomarin A

Abstract

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