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, +3

Journal of the Chemical Society Chemical Communications

Materials ScienceEngineeringNovel Azidoformate 3Fullerene SurfaceFullerene +7

Aziridino[2′,3′ : 1,2][60]fullerene

Malcolm R. Banks, J. I. G. Cadogan, Ian Gosney, +4

Journal of the Chemical Society Chemical Communications

Crystal StructureChemical EngineeringOrganic Material ChemistryEngineeringThermal Elimination +6

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, +8

Tetrahedron

Enantioselective SynthesisEngineeringNatural SciencesDiversity-oriented SynthesisChiral Auxiliary +7

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, +4

Tetrahedron Letters

Chemical TransformationsChemical EngineeringEngineeringSurface ChemistryFullerene +2

Birch reduction of C₆₀—a new appraisal

Malcolm R. Banks, Michael J. Dale, Ian Gosney, +12

Journal of the Chemical Society Chemical Communications

EngineeringForestryOrganic ChemistryBirch ReductionChemistry +15

Aziridino[2′,3′ : 1,6][60]fullerene: isolation of the first closed [5,6]-bridged fullerene adduct

Malcolm R. Banks, J. I. G. Cadogan, Ian Gosney, +6

Journal of the Chemical Society Chemical Communications

Chemical EngineeringEngineeringHeterocyclicAlkene MetathesisApplied Physics +8

Asymmetric Diels-Alder reactions employing modified camphor-derived oxazolidin-2-one chiral auxiliaries

Malcolm R. Banks, Alexander J. Blake, J. I. G. Cadogan, +4

Tetrahedron

Organic ChemistryStereoselective SynthesisChemistryAsymmetric Diels-alder ReactionsAsymmetric Catalysis +1

Preparation of enantiomerically pure fructose-derived 1,3-oxazin-2-one by INIR methodology and its application as a chiral auxiliary in some model asymmetric reactions

Malcolm R. Banks, J. I. G. Cadogan, Ian Gosney, +3

Tetrahedron

Pure Fructose-derived 1,3-Oxazin-2-oneEngineeringOrganic ChemistryStereoselective SynthesisChemistry +7

Highly regio- and stereo-specific preparation of a new carbohydrate-based 1,3-oxazin-2-one by the INIR method and its applications in some asymmetric transformations

Malcolm R. Banks, J. I. G. Cadogan, Ian Gosney, +2

Tetrahedron Asymmetry

Inir MethodStereo-specific PreparationEngineeringOrganic ChemistryStereoselective Synthesis +6

(5R)-7,8:9,10-Di-O-isopropylidene-2,6-dioxa-4-azaspiro[4,5]decan-3-one: a new chiral spirooxazolidin-2-one derived from D-(+)-galactose for use in asymmetric transformations

Malcolm R. Banks, Alexander J. Blake, J. I. G. Cadogan, +6

Journal of the Chemical Society Chemical Communications

New Chiral Spirooxazolidin-2-oneCrystalline Spirooxazolidin-2-one 2EngineeringBiochemistryNatural Sciences +13