Stereocontrolled access to optically-enriched oxabispidines

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

doi:10.1039/c2cc30761h

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 journal › Article › peer-review

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 language	English
Pages (from-to)	4836-4838
Number of pages	3
Journal	Chemical Communications
Volume	48
Issue number	40
DOIs	https://doi.org/10.1039/c2cc30761h
Publication status	Published - 18 May 2012
Externally published	Yes

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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",

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day = "18",

doi = "10.1039/c2cc30761h",

language = "English",

volume = "48",

pages = "4836--4838",

journal = "Chemical Communications",

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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

C2 - 22499212

AN - SCOPUS:84860334008

VL - 48

SP - 4836

EP - 4838

JO - Chemical Communications

JF - Chemical Communications

SN - 1359-7345

IS - 40

ER -

Stereocontrolled access to optically-enriched oxabispidines

Abstract

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