Furanodendralenes

Thomas Fallon; Anthony C. Willis; Michael N. Paddon-Row; Michael S. Sherburn

doi:10.1021/jo500458y

Furanodendralenes

Thomas Fallon, Anthony C. Willis, Michael N. Paddon-Row^*, Michael S. Sherburn

^*Corresponding author for this work

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

16 Citations (Scopus)

Abstract

An examination of Diels-Alder reactions of furan-containing analogues of dendralenes has revealed complex and fascinating reaction sequences, which chart the inherent site and stereoselectivity of these processes and give rapid access to structures of high molecular complexity.

Original language	English
Pages (from-to)	3185-3193
Number of pages	9
Journal	Journal of Organic Chemistry
Volume	79
Issue number	7
DOIs	https://doi.org/10.1021/jo500458y
Publication status	Published - 4 Apr 2014

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10.1021/jo500458y

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@article{290b74f44553472bb103168d98f0a32b,

title = "Furanodendralenes",

abstract = "An examination of Diels-Alder reactions of furan-containing analogues of dendralenes has revealed complex and fascinating reaction sequences, which chart the inherent site and stereoselectivity of these processes and give rapid access to structures of high molecular complexity.",

author = "Thomas Fallon and Willis, {Anthony C.} and Paddon-Row, {Michael N.} and Sherburn, {Michael S.}",

year = "2014",

month = apr,

day = "4",

doi = "10.1021/jo500458y",

language = "English",

volume = "79",

pages = "3185--3193",

journal = "Journal of Organic Chemistry",

issn = "0022-3263",

publisher = "American Chemical Society",

number = "7",

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TY - JOUR

T1 - Furanodendralenes

AU - Fallon, Thomas

AU - Willis, Anthony C.

AU - Paddon-Row, Michael N.

AU - Sherburn, Michael S.

PY - 2014/4/4

Y1 - 2014/4/4

N2 - An examination of Diels-Alder reactions of furan-containing analogues of dendralenes has revealed complex and fascinating reaction sequences, which chart the inherent site and stereoselectivity of these processes and give rapid access to structures of high molecular complexity.

AB - An examination of Diels-Alder reactions of furan-containing analogues of dendralenes has revealed complex and fascinating reaction sequences, which chart the inherent site and stereoselectivity of these processes and give rapid access to structures of high molecular complexity.

UR - http://www.scopus.com/inward/record.url?scp=84898077478&partnerID=8YFLogxK

U2 - 10.1021/jo500458y

DO - 10.1021/jo500458y

M3 - Article

SN - 0022-3263

VL - 79

SP - 3185

EP - 3193

JO - Journal of Organic Chemistry

JF - Journal of Organic Chemistry

IS - 7

ER -

Furanodendralenes

Abstract

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