D. Morton

发表

Synthesis of Natural-Product-Like Molecules with Over Eighty Distinct Scaffolds**

Adam Nelson, Daniel Morton, Christopher Cordier, 2008, Angewandte Chemie.

Natural products as an inspiration in the diversity-oriented synthesis of bioactive compound libraries

Adam Nelson, Daniel Morton, Christopher Cordier, 2008, Natural product reports.

Chiral non-racemic sulfinimines: versatile reagents for asymmetric synthesis

D. Morton, R. Stockman, 2006 .

Photochemical transformations of pyridinium salts: mechanistic studies and applications in synthesis.

Adam Nelson, Daniel Morton, A. Nelson, 2007, Organic & biomolecular chemistry.

Photochemical Transformations of Pyridinium Salts: Mechanistic Studies and Applications in Synthesis

A. Nelson, D. Morton, Teresa Damiano, 2007 .

An efficient method for synthesising unsymmetrical silaketals: substrates for ring-closing, including macrocycle-closing, metathesis† †Electronic supplementary information (ESI) available: Full experimental details and copies of NMR spectra for key compounds. See DOI: 10.1039/b804769n Click here for

C. Cordier, S. Warriner, A. Nelson, 2008, Organic & biomolecular chemistry.

A fluorous-tagged linker from which small molecules are released by ring-closing metathesis.

C. Cordier, S. Warriner, A. Nelson, 2008, The Journal of organic chemistry.

Natural Products as an Inspiration in the Diversity-Oriented Synthesis of Bioactive Compound Libraries

C. Cordier, A. Nelson, D. Morton, 2008 .

Metabolism of leukotriene A4 by human erythrocytes. A novel cellular source of leukotriene B4.

B. Samuelsson, F. Fitzpatrick, D. Morton, 1984, The Journal of biological chemistry.

Recent Advances in C-H Functionalization.

D. Morton, H. Davies, 2016, The Journal of organic chemistry.

Guiding principles for site selective and stereoselective intermolecular C-H functionalization by donor/acceptor rhodium carbenes.

Daniel Morton, Huw M. L. Davies, D. Morton, 2011, Chemical Society reviews.

Desymmetrisation of a centrosymmetric molecule by carbon-carbon bond formation: asymmetric aldol reactions of a centrosymmetric dialdehyde.

A. Nelson, D. Morton, R. Narquizian, 2007, Chemistry.

Collective Approach to Advancing C–H Functionalization

Huw M. L. Davies, Daniel Morton, D. Morton, 2017, ACS central science.

C-H functionalization: collaborative methods to redefine chemical logic.

D. Morton, H. Davies, 2014, Angewandte Chemie.

Direct synthesis of chiral aziridines from N-tert-butyl-sulfinylketimines.

R. Field, D. Morton, R. Stockman, 2006, Chemical communications.

Desymmetrization of a Centrosymmetric Molecule by Carbon—Carbon Bond Formation: Asymmetric Aldol Reactions of a Centrosymmetric Dialdehyde.

A. Nelson, D. Morton, R. Narquizian, 2007 .

Synthesis of chiral non-racemic substituted vinyl aziridines

A. Nadin, D. Morton, R. Stockman, 2008 .

A convenient synthesis of chiral nonracemic vinyl aziridines.

R. Field, D. Morton, R. Stockman, 2004, Organic letters.

Guiding Principles for Site Selective and Stereoselective Intermolecular C—H Functionalization by Donor/Acceptor Rhodium Carbenes

D. Morton, H. Davies, 2011 .

Novel aromatase inhibitors by structure-guided design.

Jessica Lo, Daniel Morton, Huw M. L. Davies, 2012, Journal of medicinal chemistry.

Rhodium Carbenoid InducedIntermolecular C-H Functionalization at TertiaryC-H Bonds

D. Morton, H. Davies, Zhan-Jiang Li, 2008 .

B-protected haloboronic acids for iterative cross-coupling

M. Burke, E. Gillis, D. Morton, 2009 .

Expanding the Carbene CH Insertion Toolbox

D. Morton, S. Blakey, 2015 .

Convenient method for the functionalization of the 4- and 6-positions of the androgen skeleton.

D. Ghosh, D. Morton, H. Davies, 2012, Chemical communications.