A surprising steric effect on a tandem cycloaddition/ring-opening reaction: Rapid syntheses of difluorinated analogues of (hydroxymethyl)conduritols

John Fawcett; Andrew C. Moralee; Jonathan M. Percy; Vittoria Salafia; Mark A. Vincent; Ian H. Hillier

doi:10.1039/b401245c

A surprising steric effect on a tandem cycloaddition/ring-opening reaction: Rapid syntheses of difluorinated analogues of (hydroxymethyl)conduritols

John Fawcett
, Andrew C. Moralee
, Jonathan M. Percy
, Vittoria Salafia
, Mark A. Vincent
, Ian H. Hillier

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

Abstract

Difluorinated analogues of (hydroxymethyl)conduritols can be synthesised from selected furans and a difluorinated dienophile in two reaction steps.

Original language	English
Pages (from-to)	1062-1063
Number of pages	1
Journal	Chemical Communications
Volume	10
Issue number	9
DOIs	https://doi.org/10.1039/b401245c
Publication status	Published - 7 May 2004

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10.1039/b401245c

CCDC 229969: Experimental Crystal Structure Determination
Fawcett, J. (Contributor), Moralee, A. C. (Contributor), Percy, J. M. (Contributor), Salafia, V. (Contributor), Vincent, M. A. (Contributor) & Hillier, I. (Contributor), Cambridge Crystallographic Data Centre, 1 Jan 2004
DOI: 10.5517/cc7q9cl, http://www.ccdc.cam.ac.uk/services/structure_request?id=doi:10.5517/cc7q9cl&sid=DataCite
Dataset
CCDC 229970: Experimental Crystal Structure Determination
Fawcett, J. (Contributor), Moralee, A. C. (Contributor), Percy, J. M. (Contributor), Salafia, V. (Contributor), Vincent, M. A. (Contributor) & Hillier, I. (Contributor), Cambridge Crystallographic Data Centre, 1 Jan 2004
DOI: 10.5517/cc7q9dm, http://www.ccdc.cam.ac.uk/services/structure_request?id=doi:10.5517/cc7q9dm&sid=DataCite
Dataset
CCDC 229971: Experimental Crystal Structure Determination
Fawcett, J. (Contributor), Moralee, A. C. (Contributor), Percy, J. M. (Contributor), Salafia, V. (Contributor), Vincent, M. A. (Contributor) & Hillier, I. (Contributor), Cambridge Crystallographic Data Centre, 1 Jan 2004
DOI: 10.5517/cc7q9fn, http://www.ccdc.cam.ac.uk/services/structure_request?id=doi:10.5517/cc7q9fn&sid=DataCite
Dataset

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@article{3e7b53b64311402191b4fe3ae3fb14d9,

title = "A surprising steric effect on a tandem cycloaddition/ring-opening reaction: Rapid syntheses of difluorinated analogues of (hydroxymethyl)conduritols",

abstract = "Difluorinated analogues of (hydroxymethyl)conduritols can be synthesised from selected furans and a difluorinated dienophile in two reaction steps.",

author = "John Fawcett and Moralee, \{Andrew C.\} and Percy, \{Jonathan M.\} and Vittoria Salafia and Vincent, \{Mark A.\} and Hillier, \{Ian H.\}",

year = "2004",

month = may,

day = "7",

doi = "10.1039/b401245c",

language = "English",

volume = "10",

pages = "1062--1063",

journal = "Chemical Communications",

issn = "1359-7345",

publisher = "Royal Society of Chemistry",

number = "9",

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TY - JOUR

T1 - A surprising steric effect on a tandem cycloaddition/ring-opening reaction: Rapid syntheses of difluorinated analogues of (hydroxymethyl)conduritols

AU - Fawcett, John

AU - Moralee, Andrew C.

AU - Percy, Jonathan M.

AU - Salafia, Vittoria

AU - Vincent, Mark A.

AU - Hillier, Ian H.

PY - 2004/5/7

Y1 - 2004/5/7

N2 - Difluorinated analogues of (hydroxymethyl)conduritols can be synthesised from selected furans and a difluorinated dienophile in two reaction steps.

AB - Difluorinated analogues of (hydroxymethyl)conduritols can be synthesised from selected furans and a difluorinated dienophile in two reaction steps.

U2 - 10.1039/b401245c

DO - 10.1039/b401245c

M3 - Article

SN - 1359-7345

VL - 10

SP - 1062

EP - 1063

JO - Chemical Communications

JF - Chemical Communications

IS - 9

ER -

A surprising steric effect on a tandem cycloaddition/ring-opening reaction: Rapid syntheses of difluorinated analogues of (hydroxymethyl)conduritols

Abstract

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Datasets

CCDC 229969: Experimental Crystal Structure Determination

CCDC 229970: Experimental Crystal Structure Determination

CCDC 229971: Experimental Crystal Structure Determination

Cite this