Anne GAUCHER

Dr. Anne GAUCHER

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Research Focus & Metrics

Academic Career Length

36Years (1991-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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FGFlorent Le Guern
Florent Le Guern
VMVanessa Mussard
Vanessa Mussard
AGAnne GAUCHER
Anne GAUCHER
MRMartin Rottman
Martin Rottman
DPDamien PRIM
Damien PRIM
Potential of hydrogen (pH) is one of the most relevant parameters characterizing aqueous solutions. In biology, pH is intrinsically linked to cellular life since all metabolic pathways are implicated into ionic flows. In that way, determination of local pH offers a unique and major opportunity to increase our understanding of biological systems. Whereas the most common technique to obtain these data in analytical chemistry is to directly measure potential between two electrodes, in biological systems, this information has to be recovered in-situ without any physical interaction. Based on their non-invasive optical properties, fluorescent pH-sensitive probe are pertinent tools to develop. One of the most notorious pH-sensitive probes is fluorescein. In addition to excellent photophysical properties, this fluorophore presents a pH-sensitivity around neutral and physiologic domains. This review intends to shed new light on the recent use of fluorescein as pH-sensitive probes for biological applications, including targeted probes for specific imaging, flexible monitoring of bacterial growth, and biomedical applications.

15 September 2004 in Journal of the American Chemical Society
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JMJean-Paul Mazaleyrat
Jean-Paul Mazaleyrat
KWKaren Wright
Karen Wright
AGAnne GAUCHER
Anne GAUCHER
NTNathalie Toulemonde
Nathalie Toulemonde
MWMichel Wakselman
Michel Wakselman
CTClaudio Toniolo
Claudio Toniolo

23 October 2007 in European Journal of Organic Chemistry
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Vincent TerrassonVincent Terrasson
Vincent Terrasson
JMJulien Michaux
Julien Michaux
AGAnne GAUCHER
Anne GAUCHER
JWJohny Wehbe
Johny Wehbe
SMSylvain Marque
Sylvain Marque
Jm CampagneJm Campagne
Jm Campagne

10 April 2008 in Journal of the American Chemical Society
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LDLaurence Dutot
Laurence Dutot
KWKaren Wright
Karen Wright
AGAnne GAUCHER
Anne GAUCHER
MWMichel Wakselman
Michel Wakselman
JMJean-Paul Mazaleyrat
Jean-Paul Mazaleyrat
CTClaudio Toniolo
Claudio Toniolo

14 July 2009 in Chemical Communications
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GPGrégory Pieters
Grégory Pieters
AGAnne GAUCHER
Anne GAUCHER
DPDamien Prim
Damien Prim
JMJérôme Marrot
Jérôme Marrot
The first synthesis of 6,11-diamino-[6]carbohelicenes is described: the short 5 step sequence involves Suzuki–Miyaura coupling, functional group transformations and electrophilic aromatic cyclisation; the original strategy allows the preparation of di- and tetra-substituted helicenes in comfortable yields.

6 July 2011 in Organometallics
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Journal Article
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GGGuillaume Grach
Guillaume Grach
GPGrégory Pieters
Grégory Pieters
ADAurelia Dinut
Aurelia Dinut
Vincent TerrassonVincent Terrasson
Vincent Terrasson
RMRaouf Medimagh
Raouf Medimagh
YTYves Troin
Yves Troin