THE KIMBER RESEARCH GROUP

 

58. The Kornblum DeLaMare rearrangement in natural product synthesis: 25 years of innovation

Kimber, M. C.* and Lee, D. S.* (Review)

Nat. Prod. Rep. 2024, advanced article doi.org/10/1039/D3NP00058C

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57. Synthesis of 1,3-disubstituted-[1.1.1]-bicyclopentane (BCP) salts: arylsulfonium, arylpyridinium and arylammonium isosteres

Monroe, H.; Elsegood, M. R. J.; Teat, S. J.; *Pritchard, G. J.; *Kimber, M. C.

Preprint: 2023, 10.26434/chemrxiv-2023-48v11

 

 

56. Transition metal free continuous flow synthesis of 2,5-diaryl furans: access to medicinal building blocks and optoelectronic materials​

Grantham, H. F.; Lee, R. J.; Wardas, G.; Mistry, J. -M.; Elsegood, M. R. J.; *Wright, I. A.; *Pritchard, G. P.; *Kimber, M. C.

J. Org. Chem. 2024, 89, 484.

Preprint: 2023, 10.26434/chemrxiv-2023-31ctw

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55. A family of bis-naphthyl C2-symmetric and asymmetric clefts: synthesis, solid state structure and calculation of the interplanar angle

Elgadi, G. S.; Elsegood, M. R. J.;  Patel, M.; Netz, P. A.; de Oliveira, T. E.; *Kimber, M. C. 

J. Org. Chem. 2023, 88, 3965.

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54. Concise synthesis of moracin M using Appel mediated dehydration of a bio-inspired endoperoxide

Al-Jawaheri, Y.; Elsegood, M. R. J.; Mistry, J. R.; *Kimber, M. C.

Tetrahedron Lett. 2023, 114, 154273

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53. The rearrangement of allkylallenes to 1,3-dienes

*Al-Jawaheri, Y.; *Kimber, M. C.

Reactions 2022, 3, 78 (Review).

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52. Dimeric cyclobutane formation under continuous flow conditions using organophotoredox catalysed [2+2]-cycloaddition

Grantham, H. F.; *Kimber, M. C.

ChemPhotoChem 2022, 6, eLoc. e202100219

Preprint: 10.33774/chemrxiv-2021-1c8zv

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51. A complementary approach to conjugated N-acyliminium formation through photoredox-catalyzed intermolecular radical addition to allenamides and allencarbamates  

Koleoso, O. K.; Turner, M.; Plasser, F.; *Kimber, M. C.

Beilstein J. Org. Chem. 2020, 16, 1983.

Preprint: http://doi.org/10.26434/chemrxiv.9771986.v1

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50. A general convergent strategy for the synthesis of tetra-substituted furan fatty acids (FuFAs)

Wang, Y.; *Pritchard, G. J.; *Kimber, M. C.

Eur. J. Org. Chem. 2020, 2914

Preprint: https://doi.org/10.26434/chemrxiv.11298398.v1

Highlighted on Organic Chemistry Portal October 2020.

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