Total synthesis of elaeokanine A

Hans F. Schmitthenner; Steven M. Weinreb

doi:10.1021/jo01304a054

Total synthesis of elaeokanine A

Hans F. Schmitthenner, Steven M. Weinreb

Chemistry

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

45 Scopus citations

Abstract

A new general approach to synthesis of Elaeocarpus alkaloids is discribed which utilizes the intramolecular imino Diels-Alder reaction as the key ringforming step. The methodology has been applied to total synthesis of the alkaloid Elaeokanine A.

Original language	English (US)
Pages (from-to)	3372-3373
Number of pages	2
Journal	Journal of Organic Chemistry
Volume	45
Issue number	16
DOIs	https://doi.org/10.1021/jo01304a054
State	Published - Aug 1980

All Science Journal Classification (ASJC) codes

Organic Chemistry

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10.1021/jo01304a054

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title = "Total synthesis of elaeokanine A",

abstract = "A new general approach to synthesis of Elaeocarpus alkaloids is discribed which utilizes the intramolecular imino Diels-Alder reaction as the key ringforming step. The methodology has been applied to total synthesis of the alkaloid Elaeokanine A.",

author = "Schmitthenner, \{Hans F.\} and Weinreb, \{Steven M.\}",

year = "1980",

month = aug,

doi = "10.1021/jo01304a054",

language = "English (US)",

volume = "45",

pages = "3372--3373",

journal = "Journal of Organic Chemistry",

issn = "0022-3263",

publisher = "American Chemical Society",

number = "16",

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T1 - Total synthesis of elaeokanine A

AU - Schmitthenner, Hans F.

AU - Weinreb, Steven M.

PY - 1980/8

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AB - A new general approach to synthesis of Elaeocarpus alkaloids is discribed which utilizes the intramolecular imino Diels-Alder reaction as the key ringforming step. The methodology has been applied to total synthesis of the alkaloid Elaeokanine A.

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DO - 10.1021/jo01304a054

M3 - Article

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SP - 3372

EP - 3373

JO - Journal of Organic Chemistry

JF - Journal of Organic Chemistry

IS - 16

ER -

Total synthesis of elaeokanine A

Abstract

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