Toward an MIE atlas - tools for toxicity prediction
ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY
(2015)
250
Experiments with chemists and information
ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY
(2015)
250
Defining molecular initiating events in the adverse outcome pathway framework for risk assessment
Chem Res Toxicol
(2014)
27
2100
(doi: 10.1021/tx500345j)
Synthesis of 2,3-O-benzyl-ribose and xylose and their equilibration
Tetrahedron Asymmetry
(2014)
25
1424
(doi: 10.1016/j.tetasy.2014.09.004)
Towards an MIE atlas - Definition and role
Toxicology Letters
(2014)
229
S52
(doi: 10.1016/j.toxlet.2014.06.217)
ChemInform Abstract: Reversal of Facial Selectivity in a Thia‐Claisen Rearrangement by Incorporation of a Vinylic Bromine Substituent.
ChemInform
(2014)
45
no
(doi: 10.1002/chin.201410033)
Synthesis of 2,3-O-dibenzylribo and xylosides, and their equilibriation studies; Application to oligosaccharide synthesis
ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY
(2014)
248
Reversal of facial selectivity in a thia-Claisen rearrangement by incorporation of a vinylic bromine substituent.
Organic & Biomolecular Chemistry
(2013)
11
7530
(doi: 10.1039/c3ob41580e)
International chemical identifier for reactions (RInChI) Dr Antony Williams
Journal of Cheminformatics
(2013)
5
45
(doi: 10.1186/1758-2946-5-45)
Lewis acid catalysis and ligand exchange in the asymmetric binaphthol-catalyzed propargylation of ketones.
Journal of Organic Chemistry
(2013)
78
8796
(doi: 10.1021/jo401611q)
ChemInform Abstract: Organocatalytic Domino Reaction of Cyanosulfones: Access to Complex Cyclohexane Systems with Quaternary Carbon Centers.
ChemInform
(2013)
44
no
(doi: 10.1002/chin.201331055)
Understanding the mechanism of the asymmetric propargylation of aldehydes promoted by 1,1'-bi-2-naphthol-derived catalysts.
J Am Chem Soc
(2013)
135
6142
(doi: 10.1021/ja3122137)
International chemical identifier for chemical reactions
Journal of Cheminformatics
(2013)
5
o16
(doi: 10.1186/1758-2946-5-s1-o16)
Organocatalytic domino reaction of cyanosulfones: Access to complex cyclohexane systems with quaternary carbon centers
Org Lett
(2013)
15
1386
(doi: 10.1021/ol400356k)
Combining computational and experimental methods to understand and develop asymmetric methodology in organic chemistry
ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY
(2013)
245
The formation of high-purity isocyanurate through proazaphosphatrane-catalysed isocyanate cyclo-trimerisation: computational insights
Organic & Biomolecular Chemistry
(2013)
11
90
(doi: 10.1039/c2ob26547h)
Mechanism of amination of β-keto esters by azadicarboxylates catalyzed by an axially chiral guanidine: acyclic keto esters react through an E enolate.
Journal of the American Chemical Society
(2012)
134
16869
(doi: 10.1021/ja307712y)
In Silico Inspired Total Synthesis of (−)‐Dolabriferol
Angewandte Chemie (International ed. in English)
(2012)
51
4695
(doi: 10.1002/anie.201109080)
