Highly selective synthesis of oxabicycloalkanes by indium tribromide-mediated cyclization reactions of epoxyalkenes

Brendan M. Smith; Elizabeth J. Skellam; Samantha J. Oxley; Andrew E. Graham

doi:10.1039/b707001b

Highly selective synthesis of oxabicycloalkanes by indium tribromide-mediated cyclization reactions of epoxyalkenes

Brendan M. Smith, Elizabeth J. Skellam, Samantha J. Oxley, Andrew E. Graham^*

^*Awdur cyfatebol y gwaith hwn

Cyfadran Cyfrifiadureg, Peirianneg a Gwyddoniaeth

Allbwn ymchwil: Cyfraniad at gyfnodolyn › Erthygl › adolygiad gan gymheiriaid

27 Dyfyniadau (Scopus)

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The cyclization of epoxyalkenes to oxabicycloalkanes is catalyzed by stoichiometric quantities of indium tribromide which exhibits excellent selectivity giving the oxabicyclic product in high yield in preference to other cyclized or rearrangement products.

Iaith wreiddiol	Saesneg
Tudalennau (o-i)	1979-1982
Nifer y tudalennau	4
Cyfnodolyn	Organic and Biomolecular Chemistry
Cyfrol	5
Rhif cyhoeddi	12
Dynodwyr Gwrthrych Digidol (DOIs)	https://doi.org/10.1039/b707001b
Statws	Cyhoeddwyd - 2007

Mynediad at Ddogfen

10.1039/b707001bTrwydded: CC BY-NC-ND

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@article{266bab834aa84e6386eb1bf304e32a86,

title = "Highly selective synthesis of oxabicycloalkanes by indium tribromide-mediated cyclization reactions of epoxyalkenes",

abstract = "The cyclization of epoxyalkenes to oxabicycloalkanes is catalyzed by stoichiometric quantities of indium tribromide which exhibits excellent selectivity giving the oxabicyclic product in high yield in preference to other cyclized or rearrangement products. ",

author = "Smith, {Brendan M.} and Skellam, {Elizabeth J.} and Oxley, {Samantha J.} and Graham, {Andrew E.}",

year = "2007",

doi = "10.1039/b707001b",

language = "English",

volume = "5",

pages = "1979--1982",

journal = "Organic and Biomolecular Chemistry",

issn = "1477-0520",

publisher = "Royal Society of Chemistry",

number = "12",

}

TY - JOUR

T1 - Highly selective synthesis of oxabicycloalkanes by indium tribromide-mediated cyclization reactions of epoxyalkenes

AU - Smith, Brendan M.

AU - Skellam, Elizabeth J.

AU - Oxley, Samantha J.

AU - Graham, Andrew E.

PY - 2007

Y1 - 2007

N2 - The cyclization of epoxyalkenes to oxabicycloalkanes is catalyzed by stoichiometric quantities of indium tribromide which exhibits excellent selectivity giving the oxabicyclic product in high yield in preference to other cyclized or rearrangement products.

AB - The cyclization of epoxyalkenes to oxabicycloalkanes is catalyzed by stoichiometric quantities of indium tribromide which exhibits excellent selectivity giving the oxabicyclic product in high yield in preference to other cyclized or rearrangement products.

U2 - 10.1039/b707001b

DO - 10.1039/b707001b

M3 - Article

AN - SCOPUS:34249977897

VL - 5

SP - 1979

EP - 1982

JO - Organic and Biomolecular Chemistry

JF - Organic and Biomolecular Chemistry

SN - 1477-0520

IS - 12

ER -

Highly selective synthesis of oxabicycloalkanes by indium tribromide-mediated cyclization reactions of epoxyalkenes

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