C. J. F. BICHARD - Concepedia

Author

C. J. F. BICHARD

University of Oxford

Also Known As

C. Bichard, C. J. F. BICHARD, C. J. F. Bichard, C.J.F. Bichard, Claire J. F. Bichard, Claire J.F. Bichard

Publications

536

Citations

H-Index

Concepts

All Affiliations

University of Oxford MRC Laboratory of Molecular Biology National Hellenic Research Foundation

About

C. J. F. BICHARD is an author at University of Oxford specializing in biochemistry, natural sciences, and organic chemistry.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Biochemistry	6	6	297
2	Natural Sciences	5	5	278
3	Engineering	3	3	73
4	Medicine	3	3	225
5	Biomolecular Engineering	3	3	73

C. J. F. BICHARD

Publications

518

Citations

H-Index

Page 1

	Year	Citations
Potent inhibition of glycogen phosphorylase by a spirohydantoin of glucopyranose: First pyranose analogues of hydantocidin C. J. F. BICHARD, Edward P. Mitchell, Mark R. Wormald, Tetrahedron Letters Medicinal ChemistryBiochemistryMedicineNatural SciencesGlycobiology	1995	136
Design of Inhibitors of Glycogen Phosphorylase: A Study of .alpha.- and .beta.-C-Glucosides and 1-Thio-.beta.-D-glucose Compounds Kimberly A. Watson, Edward P. Mitchell, L.N. Johnson, Biochemistry	1994	121
Glucose analogue inhibitors of glycogen phosphorylase: from crystallographic analysis to drug prediction using GRID force-field and GOLPE variable selection Kimberly A. Watson, Edward P. Mitchell, L.N. Johnson, Acta Crystallographica Section D Biological Crystallography Drug TargetAldo-keto ReductaseGlycobiologyMolecular BiologyGlucose Analogues	1995	70
N‐acetyl‐<i>β</i>‐D‐glucopyranosylamine: A potent T‐state inhibitor of glycogen phosphorylase. A comparison with <i>α</i>‐D‐glucose Nikos G. Oikonomakos, Maria Kontou, S.E. Zographos, Protein Science	1995	60
The ring contraction of δ-lactones with leaving group α-substituents: a strategy for the synthesis of 2,5-disubstituted highly functionalised homochiral tetrahydrofurans Sik-man S. Choi, Paul M. Myerscough, Antony J. Fairbanks, Journal of the Chemical Society Chemical Communications Group α-SubstituentsEngineeringBiochemistryFunctionalised Homochiral TetrahydrofuransExcellent Yield	1992	37
Acid-catalysed transformation of α-trifluoromethanesulfonates of γ- and δ-lactones into 2,5-disubstituted homochiral tetrahydrofurans Joseph R. Wheatley, C. J. F. BICHARD, Simon J. Mantell, Journal of the Chemical Society Chemical Communications 2,5-Disubstituted Homochiral TetrahydrofuransMethanolic SolutionMethyl Tetrahydrofuran-α-carboxylatesEngineeringMethanol	1993	21
Acetonides of heptonolactones: Kiliani ascension of 3-O-benzyl-D-glucose and 3-O-benzyl-D-allose C. J. F. BICHARD, Joseph R. Wheatley, George W. J. Fleet Tetrahedron Asymmetry Kiliani AscensionHeterocyclicBiochemistryNatural SciencesOrganic Chemistry	1994	20
Acetonides of α-hydroxy-δ-altronolactones C. J. F. BICHARD, Antony J. Fairbanks, George W. J. Fleet, Tetrahedron Asymmetry Organic ChemistryMain Group ChemistryEnantioselective SynthesisChemistry	1991	19
The design of potential antidiabetic drugs: experimental investigation of a number of β-D-glucose analogue inhibitors of glycogen phosphorylase N.G. Oikonomakos, Maria Kontou, S.E. Zographos, European Journal of Drug Metabolism and Pharmacokinetics Diabetes ManagementPotential Antidiabetic DrugsBiochemistryβ-D-glucose Analogue InhibitorsMedicine	1994	19
Complex tetrahydrofurans from carbohydrate lactones: easy access to epimeric C-glycosides of glucofuranose from D-glycero-D-gulo-heptono-1,4-lactone C. J. F. BICHARD, Tilmann W. Brandstetter, Juan C. Estévez, Journal of the Chemical Society Perkin Transactions 1 Bioorganic ChemistryEngineeringGlycobiologyOrganic ChemistryEpimeric C-glycosides	1996	15

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