Switching stereoselectivity in rhodium-catalysed 1,4-additions: The asymmetric synthesis of 2-substituted pyrrolizidinones

J.D. Hargrave; C.G. Frost; G. Bish

doi:10.1039/b610128c

Switching stereoselectivity in rhodium-catalysed 1,4-additions: The asymmetric synthesis of 2-substituted pyrrolizidinones

J.D. Hargrave, C.G. Frost, G. Bish

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

2 Citations (SciVal)

Abstract

The appropriate choice of organometallic nucleophile enables the straightforward preparation of different stereoisomers of 2-substituted pyrrolizidinones utilising the rhodium-catalysed 1,4-addition reaction.

Original language	English
Pages (from-to)	4389-4391
Number of pages	3
Journal	Chemical Communications
Volume	2006
Issue number	42
Early online date	2 Oct 2006
DOIs	https://doi.org/10.1039/b610128c
Publication status	Published - 2006

Access to Document

10.1039/b610128c

Cite this

@article{4ba27c0496f84584a613f7605cf2af4f,

title = "Switching stereoselectivity in rhodium-catalysed 1,4-additions: The asymmetric synthesis of 2-substituted pyrrolizidinones",

abstract = "The appropriate choice of organometallic nucleophile enables the straightforward preparation of different stereoisomers of 2-substituted pyrrolizidinones utilising the rhodium-catalysed 1,4-addition reaction. ",

author = "J.D. Hargrave and C.G. Frost and G. Bish",

year = "2006",

doi = "10.1039/b610128c",

language = "English",

volume = "2006",

pages = "4389--4391",

journal = "Chemical communications (Cambridge, England)",

issn = "1359-7345",

publisher = "Royal Society of Chemistry",

number = "42",

}

TY - JOUR

T1 - Switching stereoselectivity in rhodium-catalysed 1,4-additions

T2 - The asymmetric synthesis of 2-substituted pyrrolizidinones

AU - Hargrave, J.D.

AU - Frost, C.G.

AU - Bish, G.

PY - 2006

Y1 - 2006

N2 - The appropriate choice of organometallic nucleophile enables the straightforward preparation of different stereoisomers of 2-substituted pyrrolizidinones utilising the rhodium-catalysed 1,4-addition reaction.

AB - The appropriate choice of organometallic nucleophile enables the straightforward preparation of different stereoisomers of 2-substituted pyrrolizidinones utilising the rhodium-catalysed 1,4-addition reaction.

UR - http://www.scopus.com/inward/record.url?scp=33750238234&partnerID=8YFLogxK

UR - http://dx.doi.org/10.1039/b610128c

U2 - 10.1039/b610128c

DO - 10.1039/b610128c

M3 - Article

AN - SCOPUS:33750238234

VL - 2006

SP - 4389

EP - 4391

JO - Chemical communications (Cambridge, England)

JF - Chemical communications (Cambridge, England)

SN - 1359-7345

IS - 42

ER -

Switching stereoselectivity in rhodium-catalysed 1,4-additions: The asymmetric synthesis of 2-substituted pyrrolizidinones

Abstract

Access to Document

Other files and links

Fingerprint

HIGH RESOLUTION MASS SPECTROMETERS TO SUPPORT CHEMISTRY AT B ATH

Cite this

Switching stereoselectivity in rhodium-catalysed 1,4-additions: The asymmetric synthesis of 2-substituted pyrrolizidinones

Abstract

Access to Document

Other files and links

Fingerprint

Projects

HIGH RESOLUTION MASS SPECTROMETERS TO SUPPORT CHEMISTRY AT B ATH

Cite this