Stereocontrolled access to optically-enriched oxabispidines

Heloise Brice, Duncan M. Gill, Laura Goldie, Philip S. Keegan, William J. Kerr, Per H. Svensson

Research output: Contribution to journalArticle

8 Citations (Scopus)

Abstract

A range of chiral, optically-enriched bicyclic oxabispidines were prepared from (S)-(-)-2,3-epoxypropylphthalimide using an efficient sequence featuring a stereocontrolled intramolecular Mannich reaction as the key transformation.

Original languageEnglish
Pages (from-to)4836-4838
Number of pages3
JournalChemical Communications
Volume48
Issue number40
DOIs
Publication statusPublished - 18 May 2012
Externally publishedYes

Cite this

Brice, H., Gill, D. M., Goldie, L., Keegan, P. S., Kerr, W. J., & Svensson, P. H. (2012). Stereocontrolled access to optically-enriched oxabispidines. Chemical Communications, 48(40), 4836-4838. https://doi.org/10.1039/c2cc30761h
Brice, Heloise ; Gill, Duncan M. ; Goldie, Laura ; Keegan, Philip S. ; Kerr, William J. ; Svensson, Per H. / Stereocontrolled access to optically-enriched oxabispidines. In: Chemical Communications. 2012 ; Vol. 48, No. 40. pp. 4836-4838.
@article{fbd550cef67e4edd91e23219c24906d6,
title = "Stereocontrolled access to optically-enriched oxabispidines",
abstract = "A range of chiral, optically-enriched bicyclic oxabispidines were prepared from (S)-(-)-2,3-epoxypropylphthalimide using an efficient sequence featuring a stereocontrolled intramolecular Mannich reaction as the key transformation.",
author = "Heloise Brice and Gill, {Duncan M.} and Laura Goldie and Keegan, {Philip S.} and Kerr, {William J.} and Svensson, {Per H.}",
year = "2012",
month = "5",
day = "18",
doi = "10.1039/c2cc30761h",
language = "English",
volume = "48",
pages = "4836--4838",
journal = "Chemical Communications",
issn = "1359-7345",
publisher = "Royal Society of Chemistry",
number = "40",

}

Brice, H, Gill, DM, Goldie, L, Keegan, PS, Kerr, WJ & Svensson, PH 2012, 'Stereocontrolled access to optically-enriched oxabispidines', Chemical Communications, vol. 48, no. 40, pp. 4836-4838. https://doi.org/10.1039/c2cc30761h

Stereocontrolled access to optically-enriched oxabispidines. / Brice, Heloise; Gill, Duncan M.; Goldie, Laura; Keegan, Philip S.; Kerr, William J.; Svensson, Per H.

In: Chemical Communications, Vol. 48, No. 40, 18.05.2012, p. 4836-4838.

Research output: Contribution to journalArticle

TY - JOUR

T1 - Stereocontrolled access to optically-enriched oxabispidines

AU - Brice, Heloise

AU - Gill, Duncan M.

AU - Goldie, Laura

AU - Keegan, Philip S.

AU - Kerr, William J.

AU - Svensson, Per H.

PY - 2012/5/18

Y1 - 2012/5/18

N2 - A range of chiral, optically-enriched bicyclic oxabispidines were prepared from (S)-(-)-2,3-epoxypropylphthalimide using an efficient sequence featuring a stereocontrolled intramolecular Mannich reaction as the key transformation.

AB - A range of chiral, optically-enriched bicyclic oxabispidines were prepared from (S)-(-)-2,3-epoxypropylphthalimide using an efficient sequence featuring a stereocontrolled intramolecular Mannich reaction as the key transformation.

UR - http://www.scopus.com/inward/record.url?scp=84860334008&partnerID=8YFLogxK

U2 - 10.1039/c2cc30761h

DO - 10.1039/c2cc30761h

M3 - Article

VL - 48

SP - 4836

EP - 4838

JO - Chemical Communications

JF - Chemical Communications

SN - 1359-7345

IS - 40

ER -

Brice H, Gill DM, Goldie L, Keegan PS, Kerr WJ, Svensson PH. Stereocontrolled access to optically-enriched oxabispidines. Chemical Communications. 2012 May 18;48(40):4836-4838. https://doi.org/10.1039/c2cc30761h