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17 O NMR spectroscopy as a tool to study hydrogen bonding of cholesterol in lipid bilayers
17 O NMR spectroscopy as a tool to study hydrogen bonding of cholesterol in lipid bilayers
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17 O NMR spectroscopy as a tool to study hydrogen bonding of cholesterol in lipid bilayers

Rowlands, Lucy J. ; Marks, Adam ; Sanderson, John M. ; Law, Robert V.

Chemical communications (Cambridge, England), 2020-11, Vol.56 (92), p.14499-14502 [Peer Reviewed Journal]

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17O NMR spectroscopy as a tool to study hydrogen bonding of cholesterol in lipid bilayers
17O NMR spectroscopy as a tool to study hydrogen bonding of cholesterol in lipid bilayers
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17O NMR spectroscopy as a tool to study hydrogen bonding of cholesterol in lipid bilayers

Rowlands, Lucy J ; Marks, Adam ; Sanderson, John M ; Law, Robert V

Chemical communications (Cambridge, England), 2020-11, Vol.56 (92), p.14499-14502 [Peer Reviewed Journal]

Cambridge: Royal Society of Chemistry

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3
O NMR spectroscopy as a tool to study hydrogen bonding of cholesterol in lipid bilayers
O NMR spectroscopy as a tool to study hydrogen bonding of cholesterol in lipid bilayers
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O NMR spectroscopy as a tool to study hydrogen bonding of cholesterol in lipid bilayers

Rowlands, Lucy J ; Marks, Adam ; Sanderson, John M ; Law, Robert V

Chemical communications (Cambridge, England), 2020-11, Vol.56 (92), p.14499-1452 [Peer Reviewed Journal]

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4
The synthesis of enantiomerically pure 4-substituted [2.2]paracyclophane derivatives by sulfoxide-metal exchange
The synthesis of enantiomerically pure 4-substituted [2.2]paracyclophane derivatives by sulfoxide-metal exchange
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The synthesis of enantiomerically pure 4-substituted [2.2]paracyclophane derivatives by sulfoxide-metal exchange

Hitchcock, Peter B ; Rowlands, Gareth J ; Parmar, Rakesh

Chemical communications (Cambridge, England), 2005-09 (33), p.4219-4221 [Peer Reviewed Journal]

England

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5
Chiral sulfoxides in the enantioselective allylation of aldehydes with allyltrichlorosilane
Chiral sulfoxides in the enantioselective allylation of aldehydes with allyltrichlorosilane
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Chiral sulfoxides in the enantioselective allylation of aldehydes with allyltrichlorosilane

Rowlands, Gareth J ; Kentish Barnes, William

Chemical communications (Cambridge, England), 2003-11 (21), p.2712-2713 [Peer Reviewed Journal]

England

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6
5-endo-trig Cyclisations in heterocycle synthesis: enantiospecific synthesis of (+)-monomorine I
5-endo-trig Cyclisations in heterocycle synthesis: enantiospecific synthesis of (+)-monomorine I
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5-endo-trig Cyclisations in heterocycle synthesis: enantiospecific synthesis of (+)-monomorine I

Berry, Malcolm B. ; Rowlands, Gareth J. ; Craig, Donald ; Jones, Philip S.

Chemical communications (Cambridge, England), 1997 (22), p.2141-2142 [Peer Reviewed Journal]

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7
EPR study of the H2O2 interaction with TiO2; evidence for a novel S = 1 surface radical pair
EPR study of the H2O2 interaction with TiO2; evidence for a novel S = 1 surface radical pair
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EPR study of the H2O2 interaction with TiO2; evidence for a novel S = 1 surface radical pair

Murphy, Damien M. ; Griffiths, Emyr W. ; Rowlands, Christopher C. ; Hancock, Fred E. ; Giamello, Elio

Chemical communications (Cambridge, England), 1997 (22), p.2177-2178 [Peer Reviewed Journal]

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8
The tethered Biginelli condensation in natural product synthesis
The tethered Biginelli condensation in natural product synthesis
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The tethered Biginelli condensation in natural product synthesis

Aron, Zachary D ; Overman, Larry E

Chemical communications (Cambridge, England), 2004-02 (3), p.253-265 [Peer Reviewed Journal]

England

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9
Cyanine dye mediated mitochondrial targeting enhances the anti-cancer activity of small-molecule cargoes
Cyanine dye mediated mitochondrial targeting enhances the anti-cancer activity of small-molecule cargoes
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Cyanine dye mediated mitochondrial targeting enhances the anti-cancer activity of small-molecule cargoes

Nödling, Alexander R ; Mills, Emily M ; Li, Xuefei ; Cardella, Davide ; Sayers, Edward J ; Wu, Shih-Hsiung ; Jones, Arwyn T ; Luk, Louis Y. P ; Tsai, Yu-Hsuan

Chemical communications (Cambridge, England), 2020-04, Vol.56 (34), p.4672-4675 [Peer Reviewed Journal]

England: Royal Society of Chemistry

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10
Progress toward colorimetric and fluorescent detection of carbonyl sulfide
Progress toward colorimetric and fluorescent detection of carbonyl sulfide
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Progress toward colorimetric and fluorescent detection of carbonyl sulfide

Cerda, Matthew M ; Fehr, Julia M ; Sherbow, Tobias J ; Pluth, Michael D

Chemical communications (Cambridge, England), 2020-08, Vol.56 (67), p.9644-9647 [Peer Reviewed Journal]

Cambridge: Royal Society of Chemistry

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