80) Desymmetrization of Meso-bisphosphates via Rhodium Catalyzed Asymmetric Allylic Arylation.
Reece Jacques, Alexander M. L. Hell, Robert D. C. Pullin, Stephen P. Fletcher
Tetrahedron 2019, DOI: 10.1016/j.tet.2019.130560.

79) Retooling Asymmetric Conjugate Additions for Sterically Demanding Substrates with an Iterative Data-Driven Approach.
Alexandre Brethomé, Robert S. Paton, Stephen P. Fletcher
ACS Catalysis 2019, DOI: 10.1021/acscatal.9b01814.

78) Enantio‐ and Diastereoselective Suzuki‐Miyaura Coupling with Racemic Bicycles.
Friedrich Wieland Goetzke Mike Mortimore Stephen P. Fletcher
Angewandte Chemie 2019, DOI: 10.1002/anie.201906478.

77) Highly Enantioselective Hiyama Cross-Coupling via Rh-Catalyzed Allylic Arylation of Racemic Allyl Chlorides.
Jesus Gonzalez, Philipp Schafer, and Stephen P. Fletcher
Organometallics 2019, DOI: 10.1021/acs.organomet.9b00197.

76) A chemically fuelled self-replicator.
Sarah M. Morrow, Ignacio Colomer & Stephen P. Fletcher
Nature Communications 2019, 10, 1011.

75) Conformational Effects on Physical-Organic Descriptors: The Case of Sterimol Steric Parameters.
A. V. Brethomé, S. P. Fletcher and R. S. Paton
ACS Catalysis 2019, 9, 2313–2323.

74) Controlling the Kinetics of Self-Reproducing Micelles by Catalyst Compartmentalization in a Biphasic System.
Elias A. J. Post and Stephen P Fletcher
J. Org. Chem. 2019, 84, 2741–2755.

73) Desymmetrization of meso-bisphosphates using copper catalysis and alkylzirconocene nucleophiles.
R. Jacques, R. Pullin and S. P. Fletcher
Nature Communications 2019, 10, 21.

72) β-Chloroaldehydes from Trapping Zirconium Enolates Produced in Asymmetric 1, 4-Additions.
Jiao Yu Joseph Wang, Thomas Palacin, and Stephen P. Fletcher
Organic Letters 2019, 21, 378–381.

71) Self-reproducing micelles coupled to a secondary catalyst.
Elias Post, Andrew Bissette and Stephen P. Fletcher
Chem. Commun. 2018, 54, 8777-8780.

70) A transient self-assembling self-replicator.
Ignacio Colomer, Sarah M. Morrow & Stephen P. Fletcher
Nature Communications 2018, 9, 2239.

69) Catalytic Asymmetric Synthesis of Geminal-Dicarboxylates.
Nisha Mistry and Stephen P. Fletcher
Chem. Sci., 2018, 9, 6307.

68) Construction of β to carbonyl stereogenic centres by asymmetric 1,4-addition of alkylzirconocenes to dienones and ynenones.
Zhenbo Gao and Stephen Patrick Fletcher
Chem. Commun. 2018, 54, 3601.

67) Molecular machines for catalysis.
Lucy van Dijk, Michael J. Tilby, Robert Szpera, Owen A. Smith, Holly A. P. Bunce & Stephen P. Fletcher
Nature Reviews Chemistry 2018 , 2, 117.

66) Formation of quaternary centres by copper catalysed asymmetric conjugate addition to β-substituted cyclopentenones with the aid of a quantitative structure–selectivity relationship.
Ruchuta Ardkhean, Mike Mortimore, Robert S. Paton and Stephen P. Fletcher
Chem. Sci. 2018, 9, 2628-2632.

65) Asymmetric cross-coupling of alkyl, alkenyl and (hetero)aryl nucleophiles with racemic allyl halides.
P. Schäfer, M. Sidera, T. Palacin and S. P. Fletcher
Chem. Commun. 2017, 5312499–12511.
Feature Article and Cover Article. (cover)

64) Asymmetric conjugate addition of alkylzirconium reagents to α,β-unsaturated thioesters: access to fragrances and acyclic stereochemical arrays.
Z. Gao and S. P. Fletcher
Chem. Commun. 2017, 5310216–10219.

63) Enantioselective conjugate addition catalyzed by a copper-phosphoramidite complex: Computational and experimental exploration of asymmetric induction.
R. Ardkhean, P. M. C. Roth, R. M. Maksymowicz, A. Curran, Q. Peng, R. S. Paton and S. P. Fletcher
ACS Catal. 2017, 76729–6737.

62) Potential for minimal self-replicating systems in a dynamic combinatorial library of equilibrating imines​.
S. M. Morrow, A. J. Bissette and S. P. Fletcher
Tetrahedron 2017, 735005–5010.
Symposium-in-Print on Dynamic Functional Molecular Systems dedicated to Ben Feringa

61) Asymmetric Suzuki–Miyaura coupling of heterocycles via Rhodium-catalyzed allylic arylation of racemates.
P. Schäfer, T. Palacin, M. Sidera and S. P. Fletcher
Nature Commun. 2017, 815762.

60) Transmission of chirality through space and across length scales.
S. M. Morrow, A. J. Bissette and S. P. Fletcher
Nature Nanotechnol. 2017, 12, 410–419.

59) Mechanistic Studies on a Cu-Catalyzed Asymmetric Allylic Alkylation with Cyclic Racemic Starting Materials.
E. Rideau, H. You, M. Sidera. T. D. W. Claridge and S. P. Fletcher
J. Am. Chem. Soc. 2017139, 5614–5624.

58) High-Power Actuation from Molecular Photoswitches in Enantiomerically Paired Soft Springs​.
S. J. Aßhoff, F. Lancia, S. Iamsaard, B. Matt, T. Kudernac, S. P. Fletcher and N. Katsonis
Angew. Chem. Int. Ed. 2017, 563261–3265. 'Very Important Paper'
Highlighted in C&EN 2017, 95, 11

57) Acyclic Quaternary Centers from Asymmetric Conjugate Addition of Alkylzirconium Reagents to Linear Trisubstituted Enones​.
Z. Gao and S. P. Fletcher
Chem. Science 2017, 8, 641–646.
Highlighted in Synfacts 2016, 12, 1271.

56) Visualization of the spontaneous emergence of a complex, dynamic, and autocatalytic system.
J. Ortega-Arroyo, A. J. Bissette, P. Kukura and  S. P. Fletcher
Proc. Natl. Acad. Sci. U. S. A. 2016, 113, 11122–11126.

55) Preparation of biomimetic photoresponsive polymer springs.
S. Iamsaard, E. Villemin, F. Lancia, S.-J. Aßhoff, S. P. Fletcher and N. Katsonis
Nature Protoc. 2016, 11, 1788–1797.

54) Cp2ZrMeCl: A Reagent for Asymmetric Methyl Addition.
K. Garrec and S. P. Fletcher
Org. Lett. 2016, 18, 3814–3817.
Highlighted as Synfact of the Month.

53) Fluorinated Azobenzenes for Shape-Persistent Liquid Crystal Polymer Networks
S. Iamsaard, E. Anger, S. J. Aßhoff, A. Depauw, S. P. Fletcher, and N. Katsonis
Angew. Chem. Int. Ed. 2016, 55, 9908–9912. 'Hot Paper'

52) Phosphoramidite Ligands Based on Simple 1,2-Diols: Synthesis, Use in Copper-Catalyzed Asymmetric Additions, and Achirotopic Stereogenic Phosphorus Centres​.
N. Mistry and S. P. Fletcher
Adv. Synth. Catal. 2016, 358, 2489–2496.

51) Living and immortal polymerization of seven and six membered lactones to high molecular weights with aluminum salen and salan catalysts​.
J. P. MacDonald, M. Sidera, S. P. Fletcher and M. P. Shaver
Eur. Polym. J. 2016, 74, 287–295.