Hitesh J. Sanganee - Concepedia

Author

Hitesh J. Sanganee

Also Known As

H J Sanganee, H Sanganee, H. J. SANGANEE, H. Sanganee, HITESH SANGANEE, Hitesh J Sanganee, Hitesh J. Sanganee, Hitesh Sanganee, Maria Ryaboshapkina, Sanganee, H.J.

Publications

1.8K

Citations

H-Index

Concepts

All Affiliations

AstraZeneca (United Kingdom)University of Oxford Loughborough University AstraZeneca (Sweden)AstraZeneca (Singapore)

About

Hitesh J. Sanganee is an author at AstraZeneca (United Kingdom) specializing in organic chemistry, pharmacology, and chemistry.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Engineering	11	11	616
2	Medicine	11	11	513
3	Natural Sciences	7	7	466
4	Health Sciences	2	2	35
5	Allergy	1	1	14

Hitesh J. Sanganee

Publications

1.4K

Citations

H-Index

Page 1

	Year	Citations
Screening of a library of phage-displayed peptides identifies human Bcl-2 as a taxol-binding protein 1 1Edited by I. A. Wilson Diane J. Rodi, Robert W. Janes, Hitesh J. Sanganee, Journal of Molecular Biology Protein FunctionSignal TransductionBiochemistryG Protein-coupled ReceptorMedicine	1999	221
4-Substituted-5,5-dimethyl oxazolidin-2-ones as effective chiral auxiliaries for enolate alkylations and Michael additions Stephen G. Davies, Hitesh J. Sanganee Tetrahedron Asymmetry EngineeringMichael AdditionsPharmacologyOrganic ChemistryStereoselective Synthesis	1995	100
Asymmetric alkylations using SuperQuat auxiliaries—an investigation into the synthesis and stability of enolates derived from 5,5-disubstituted oxazolidin-2-ones Steven D. Bull, Stephen G. Davies, Simon Jones, Journal of the Chemical Society Perkin Transactions 1 Asymmetric CatalysisEngineeringHomochiral 4-Isopropyl-5,5-dimethyloxazolidin-2-one5,5-Disubstituted Oxazolidin-2-onesChiral Auxiliary	1999	86
One-Pot Catalytic Enantioselective Synthesis of Tetrahydropyridines via a Nitro-Mannich/Hydroamination Cascade David M. Barber, Hitesh J. Sanganee, Darren J. Dixon Organic Letters Chemical EngineeringUseful Tetrahydropyridine DerivativesEngineeringNovel OrganocatalystsOne-pot Nitro-mannich/hydroamination Cascade	2012	71
The ?SuperQuat? (R)-4-phenyl-5,5-dimethyl oxazolidin-2-one as an effective chiral auxiliary for conjugate additions: Asymmetric synthesis of (?)-Aplysillamide B Stephen G. Davies, Hitesh J. Sanganee, Peter Szolcsányi Tetrahedron EngineeringAsymmetric Synthesis-Aplysillamide BEffective Chiral AuxiliaryOrganic Chemistry	1999	70
A Practical Procedure for the Multigram Synthesis of the SuperQuat Chiral Auxiliaries Steven D. Bull, Stephen G. Davies, Simon Jones, Synlett Superquat Chiral AuxiliariesRapid AccessEngineeringNatural SciencesDiversity-oriented Synthesis	1998	69
One-pot nitro-Mannich/hydroamination cascades for the direct synthesis of 2,5-disubstituted pyrroles using base and gold catalysis David M. Barber, Hitesh J. Sanganee, Darren J. Dixon Chemical Communications Chemical EngineeringOne-pot Reaction CascadeEngineeringOrganic ChemistryCatalysis	2011	61
SuperQuat N-acyl-5,5-dimethyloxazolidin-2-ones for the asymmetric synthesis of α-alkyl and β-alkyl aldehydes Steven D. Bull, Stephen G. Davies, Rebecca L. Nicholson, Organic & Biomolecular Chemistry	2003	54
Cathepsin C Inhibitors: Property Optimization and Identification of a Clinical Candidate Mark Furber, A.K. Tiden, Philip Gardiner, Journal of Medicinal Chemistry Drug TargetCathepsin C InhibitorsLead IdentificationClinical CandidatePharmacotherapy	2014	54
One-Pot Asymmetric Nitro-Mannich/Hydroamination Cascades for the Synthesis of Pyrrolidine Derivatives: Combining Organocatalysis and Gold Catalysis David M. Barber, Andrej Ďuriš, Amber L. Thompson, ACS Catalysis Chemical EngineeringCascade ApproachEngineeringNovel OrganocatalystsOne-pot Nitro-mannich/hydroamination Cascade	2014	53

Page 1