Copper-catalysed meso-bislactone ring opening using Grignard and mixed triorganozinc reagents

Scott Borthwick; Wolfgang Dohle; Paul R. Hirst; Kevin I. Booker-Milburn

doi:10.1016/j.tetlet.2006.07.146

Copper-catalysed meso-bislactone ring opening using Grignard and mixed triorganozinc reagents

Scott Borthwick, Wolfgang Dohle, Paul R. Hirst, Kevin I. Booker-Milburn^*

^*Corresponding author for this work

Research output: Contribution to journal › Article (Academic Journal) › peer-review

16 Citations (Scopus)

Abstract

An efficient copper-mediated S _N2′ ring-opening reaction of a meso-bislactone has been developed using Grignard reagents and, for the first time, mixed triorganozinc reagents. © 2006 Elsevier Ltd. All rights reserved.

Translated title of the contribution	Copper-catalysed meso-bislactone ring opeingin using Grignard and mixed triorganozinc reagents
Original language	English
Pages (from-to)	7205-7208
Number of pages	4
Journal	Tetrahedron Letters
Volume	47
Issue number	40
DOIs	https://doi.org/10.1016/j.tetlet.2006.07.146
Publication status	Published - 2 Oct 2006

Bibliographical note

Publisher: Elsevier

Keywords

Desymmetrisation
Grignard
meso-Bislactone
Organocopper
Organozinc

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title = "Copper-catalysed meso-bislactone ring opening using Grignard and mixed triorganozinc reagents",

abstract = "An efficient copper-mediated S N2′ ring-opening reaction of a meso-bislactone has been developed using Grignard reagents and, for the first time, mixed triorganozinc reagents. {\textcopyright} 2006 Elsevier Ltd. All rights reserved.",

keywords = "Desymmetrisation, Grignard, meso-Bislactone, Organocopper, Organozinc",

author = "Scott Borthwick and Wolfgang Dohle and Hirst, {Paul R.} and Booker-Milburn, {Kevin I.}",

note = "Publisher: Elsevier",

year = "2006",

month = oct,

day = "2",

doi = "10.1016/j.tetlet.2006.07.146",

language = "English",

volume = "47",

pages = "7205--7208",

journal = "Tetrahedron Letters",

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T1 - Copper-catalysed meso-bislactone ring opening using Grignard and mixed triorganozinc reagents

AU - Borthwick, Scott

AU - Dohle, Wolfgang

AU - Hirst, Paul R.

AU - Booker-Milburn, Kevin I.

N1 - Publisher: Elsevier

PY - 2006/10/2

Y1 - 2006/10/2

N2 - An efficient copper-mediated S N2′ ring-opening reaction of a meso-bislactone has been developed using Grignard reagents and, for the first time, mixed triorganozinc reagents. © 2006 Elsevier Ltd. All rights reserved.

AB - An efficient copper-mediated S N2′ ring-opening reaction of a meso-bislactone has been developed using Grignard reagents and, for the first time, mixed triorganozinc reagents. © 2006 Elsevier Ltd. All rights reserved.

KW - Desymmetrisation

KW - Grignard

KW - meso-Bislactone

KW - Organocopper

KW - Organozinc

UR - http://www.scopus.com/inward/record.url?scp=33747876134&partnerID=8YFLogxK

U2 - 10.1016/j.tetlet.2006.07.146

DO - 10.1016/j.tetlet.2006.07.146

M3 - Article (Academic Journal)

SN - 0040-4039

VL - 47

SP - 7205

EP - 7208

JO - Tetrahedron Letters

JF - Tetrahedron Letters

IS - 40

ER -

Copper-catalysed meso-bislactone ring opening using Grignard and mixed triorganozinc reagents

Abstract

Bibliographical note

Keywords

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TOTAL SYNTHESIS WITHOUT PROTECTING GROUPS: THE ALKALOIDS OF TUBEROSA STEMONA

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Copper-catalysed meso-bislactone ring opening using Grignard and mixed triorganozinc reagents

Abstract

Bibliographical note

Keywords

Access to Document

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Fingerprint

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TOTAL SYNTHESIS WITHOUT PROTECTING GROUPS: THE ALKALOIDS OF TUBEROSA STEMONA

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