Malcolm R. Banks

Bis-functionalisation of C₆₀via thermal rearrangement of an isolable fulleroaziridine bearing a ‘solubilising’ supermesityl ester moiety

Malcolm R. Banks, J. I. G. Cadogan, Ian Gosney et al. · Journal of the Chemical Society Chemical Communications · 1994 · 57 citations

Materials Science, Engineering, Novel Azidoformate 3 +9

Aziridino[2′,3′ : 1,2][60]fullerene

Malcolm R. Banks, J. I. G. Cadogan, Ian Gosney et al. · Journal of the Chemical Society Chemical Communications · 1995 · 51 citations

Crystal Structure, Chemical Engineering, Organic Material Chemistry +8

Enantiospecific preparation of [(2r,6s)-endo]-5-aza-1,10,10-trimethyl-3-oxatricyclo[5.2.1.02,6]decan-4-one by a nitrene-mediated route from [(1s)-endo]-(−)-borneol and its utility as a chiral auxiliary in some asymmetric transformations

Malcolm R. Banks, Alexander J. Blake, J. I. G. Cadogan et al. · Tetrahedron · 1992 · 51 citations

Enantioselective Synthesis, Engineering, Natural Sciences +9

Chemical transformations on the surface of [60]fullerene: Synthesis of [60]fullereno[1′,2′:4,5]oxazolidin-2-one

Malcolm R. Banks, J. I. G. Cadogan, Ian Gosney et al. · Tetrahedron Letters · 1994 · 45 citations

Chemical Transformations, Chemical Engineering, Engineering +4

Birch reduction of C₆₀—a new appraisal

Malcolm R. Banks, Michael J. Dale, Ian Gosney et al. · Journal of the Chemical Society Chemical Communications · 1993 · 40 citations

Engineering, Forestry, Organic Chemistry +17