Matthew J Gaunt University Of Cambridge

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Professor Matthew Gaunt Yusuf Hamied Department Of Chemistry

Matthew Gaunt Department of Chemistry University of Cambridge Lensfield Road Cambridge CB2 1EW United Kingdom Email.

Matthew j gaunt university of cambridge. Gaunt Department of Chemistry University of Cambridge Lensfield Road CB2 1EW UK aarondtprincetonedu dr443camacuk mjg32camacuk Acknowledgements. The group in Autumn 2018. Smith Junior Research Fellow at University of Cambridge 2001 Promoted to Professor in October.

101039D1SC04554G This article is licensed under a Creative Commons Attribution-NonCommercial 30 Unported Licence. Ala Bunescu 1 Yusra Abdelhamid 1 Matthew J Gaunt 2 Affiliations 1 Yusuf Hamied Department of Chemistry University of Cambridge Lensfield Road Cambridge CB2 1EW United Kingdom. Palladium-catalysed C-H activation of aliphatic amines to give strained nitrogen heterocycles Nature 2014 510 129.

New Catalytic Strategies for Chemical Synthesis Despite the changing face of chemistry the importance of synthesis - the ability to generate molecules in a controlled fashion - has not diminished. A Steric Tethering Approach Enables Palladium-Catalysed C-H Activation of Primary Amino Alcohols Nature Chem. Yusuf Hamied Department of Chemistry University of Cambridge Lensfield Road Cambridge CB2 1EW United Kingdom.

We report a common strategy to facilitate the syntheses of the polycyclic alkaloids -FR901483 1 and -TAN1251C 2A divergent synthetic strategy provides access to both natural products through a pivotal spirolactam intermediate 3 which can be accessed on a gram-scaleA photocatalytic olefin hydroaminoalkylation brings together three readily available building blocks and. Matthew J Gaunts 138 research works with 11124 citations and 4531 reads including. Boschetti Jinquan Yu Jonathan B.

Gaunt MJ Yu J Spencer JB. We are particularly focused on palladium-catalyzed CH activation of aliphatic molecules photoredox catlaysis for alkylamine synthesis and high oxidation copper catalysis. We are grateful to AstraZeneca Pfizer and the EPSRC AKP FO RHS and MJG and the ERC MJG for fellowships.

Spencer Preferential Hydrogenolysis of NAP Esters Provides a New Orthogonal Protecting Group Strategy for Carboxylic Acids Tetrahedron Lett. Robert J Phipps 1 Matthew J Gaunt. Eric Schelter Pat Walsh gp8073 Joint Postdoc with Scholes.

Gaunt University of Cambridge Graduated University of Birmingham 1995 Ph. University of Cambridge Department of Chemistry Cambridge United Kingdom. Selective chemical functionalization of N6-methyladenine in DNA.

Spencer Postdoctoral Fellow at University of Pennsylvania 1999 - 2001 Advisor. Eleven postdocs seventeen PhD students three Part III students and one member of support staff. University of Cambridge 2020 Advisor.

Preferential hydrogenolysis of NAP esters provides a new orthogonal protecting group strategy for carboxylic acids Tetrahedron Letters. Ley University of Cambridge as a. University of Toronto 2020 Advisor.

I am a synthetic organic chemistry at the University of Cambridge. We report a new Pd II-catalyzed C-H bond amination reaction to form carbazoles an important motif that is prevalent in a range of systems. Gaunt MJ Boschetti CE Yu J Spencer JB.

Sci 2021 12 12812 DOI. 101126science1169975 Abstract For over a century chemical transformations of benzene derivatives have been guided by the high selectivity for electrophilic attack at the orthopara. However the increasingly complex synthetic problems being posed by nature medicine and materials demand new reactivity concepts and strategies in order to meet these challenges.

Our group aims to develop novel methodologies and technologies for organic synthesis. 44 1223336442 Search for more papers by this author Matthew J. Current areas of interest include.

Matthew Gaunt graduated from the University of Birmingham with First Class Honours for Chemistry in 1995. Carin C C Johansson. Gaunt University of Cambridge Frank Glorius Universität Münster Lukas J.

Reich and Matthew J. Affiliation 1 Department of Chemistry University of Cambridge Lensfield Road Cambridge CB2 1EW UK. We thank the EPSRC Mass Spectrometry Service at the.

2001 - 2003 Postdoctoral research with Professor Steven V. We are grateful to AstraZeneca the Herchel Smith Fund and the Royal Society for funding. Goossen Universität Bochum Véronique Gouverneur University of Oxford Stephen Hashmi Ruprecht-Karls-Universität Heidelberg Yujiro Hayashi Tohoku University Kenichiro Itami Nagoya University Timothy Jamison Massachusetts Institute of Technology Cambridge.

Department of Chemistry University of Cambridge Lensfield Road Cambridge CB2 1EW UK Fax. He subsequently completed his PhD studies under the supervision of Dr Jonathan Spencer at the University of Cambridge as a Wellcome Trust Scholar in 1999. 1999 40 1803 101016S0040-40399900014-3.

X-ray crystallography data was collected and solved by Peter D. Title of LectureNew Strategies for. University of Cambridge to begin independent research.

There are currently thirty-two members of the group. View information of former group members. Ala Bunescu Yusra Abdelhamid Matthew J.

My research group is interested in the development of new chemical reactivity ideas using catalysis. D from University of Cambridge 1999 Advisor. Michael T Taylor 1 Jennifer E Nelson 1 Marcos G Suero 1 Matthew J Gaunt 2 Affiliations 1 Department of Chemistry University of Cambridge Cambridge UK.

Mass spectrometry data were acquired at the EPSRC UK National Mass Spectrometry Facility at Swansea University. University of Pennsylvania 2021 Advisors.

Professor Matthew Gaunt Yusuf Hamied Department Of Chemistry