Facile Bridged Bicycloalkane Synthesis via Intramolecular Nitrone-Olefin Cycloaddition

Raymond L. Funk; Linus H.M. Horcher; Joy Umstead Daggett; Marvin M. Hansen

doi:10.1021/jo00163a052

Facile Bridged Bicycloalkane Synthesis via Intramolecular Nitrone-Olefin Cycloaddition

Raymond L. Funk, Linus H.M. Horcher, Joy Umstead Daggett, Marvin M. Hansen

Chemistry

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

18 Scopus citations

Abstract

Exocyclic nitrones smoothly participate in intramolecular cycloaddition reactions to provide bridged bicycloalkanes. The application of this methodology in the first total synthesis of the antifertility agent (±)-7,12-secoishwaran-12-ol is also discussed.

Original language	English (US)
Pages (from-to)	2632-2634
Number of pages	3
Journal	Journal of Organic Chemistry
Volume	48
Issue number	15
DOIs	https://doi.org/10.1021/jo00163a052
State	Published - Jul 1983

All Science Journal Classification (ASJC) codes

Organic Chemistry

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10.1021/jo00163a052

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@article{4835f8641655413280ffe7252816e84e,

title = "Facile Bridged Bicycloalkane Synthesis via Intramolecular Nitrone-Olefin Cycloaddition",

abstract = "Exocyclic nitrones smoothly participate in intramolecular cycloaddition reactions to provide bridged bicycloalkanes. The application of this methodology in the first total synthesis of the antifertility agent (±)-7,12-secoishwaran-12-ol is also discussed.",

author = "Funk, {Raymond L.} and Horcher, {Linus H.M.} and Daggett, {Joy Umstead} and Hansen, {Marvin M.}",

year = "1983",

month = jul,

doi = "10.1021/jo00163a052",

language = "English (US)",

volume = "48",

pages = "2632--2634",

journal = "Journal of Organic Chemistry",

issn = "0022-3263",

publisher = "American Chemical Society",

number = "15",

}

TY - JOUR

T1 - Facile Bridged Bicycloalkane Synthesis via Intramolecular Nitrone-Olefin Cycloaddition

AU - Funk, Raymond L.

AU - Horcher, Linus H.M.

AU - Daggett, Joy Umstead

AU - Hansen, Marvin M.

PY - 1983/7

Y1 - 1983/7

N2 - Exocyclic nitrones smoothly participate in intramolecular cycloaddition reactions to provide bridged bicycloalkanes. The application of this methodology in the first total synthesis of the antifertility agent (±)-7,12-secoishwaran-12-ol is also discussed.

AB - Exocyclic nitrones smoothly participate in intramolecular cycloaddition reactions to provide bridged bicycloalkanes. The application of this methodology in the first total synthesis of the antifertility agent (±)-7,12-secoishwaran-12-ol is also discussed.

UR - http://www.scopus.com/inward/record.url?scp=0345547154&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=0345547154&partnerID=8YFLogxK

U2 - 10.1021/jo00163a052

DO - 10.1021/jo00163a052

M3 - Letter

AN - SCOPUS:0345547154

SN - 0022-3263

VL - 48

SP - 2632

EP - 2634

JO - Journal of Organic Chemistry

JF - Journal of Organic Chemistry

IS - 15

ER -

Facile Bridged Bicycloalkane Synthesis via Intramolecular Nitrone-Olefin Cycloaddition

Abstract

All Science Journal Classification (ASJC) codes

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