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Hitesh J. Sanganee
Observed names:
H J Sanganee,
H Sanganee,
H. J. SANGANEE,
H. Sanganee,
HITESH SANGANEE,
Hitesh J Sanganee,
Hitesh Sanganee,
Sanganee, H.J.,
Sanganee, Hitesh J.
show all 9
Institutions:
AstraZeneca (United Kingdom),
Alexion Pharmaceuticals (United States)
Observed institutions:
Florida State University,
AstraZeneca (United Kingdom),
University of Michigan,
Melbourn Science Park,
University of Oxford,
Alexion Pharmaceuticals (United States),
Tianjin Medical University
show all 7
OpenAlex ID:
A5020130403
Screening of a library of phage-displayed peptides identifies human Bcl-2 as a taxol-binding protein 1 1Edited by I. A. Wilson
1999
·
Diane J Rodi
, Robert W Janes
, et al.
·
Journal of Molecular Biology
·
224
Rare variant associations with plasma protein levels in the UK Biobank
2023
·
Ryan S. Dhindsa
, Oliver S. Burren
, et al.
·
Nature
·
189
PDF
An Integrated Approach to Fragment-Based Lead Generation:Philosophy, Strategy and Case Studies from AstraZenecas Drug Discovery Programmes
2007
·
Jeffrey Albert
, Niklas Blomberg
, et al.
·
Current Topics in Medicinal Chemistry
·
126
4-Substituted-5,5-dimethyl oxazolidin-2-ones as effective chiral auxiliaries for enolate alkylations and Michael additions
1995
·
Stephen G. Davies
, Hitesh J. Sanganee
·
Tetrahedron Asymmetry
·
102
Asymmetric alkylations using SuperQuat auxiliaries—an investigation into the synthesis and stability of enolates derived from 5,5-disubstituted oxazolidin-2-ones
1999
·
Steven D. Bull
, Stephen G. Davies
, et al.
·
Journal of the Chemical Society Perkin Transactions 1
·
87
One-Pot Catalytic Enantioselective Synthesis of Tetrahydropyridines via a Nitro-Mannich/Hydroamination Cascade
2012
·
David M. Barber
, Hitesh J. Sanganee
, et al.
·
Organic Letters
·
73
The ?SuperQuat? (R)-4-phenyl-5,5-dimethyl oxazolidin-2-one as an effective chiral auxiliary for conjugate additions: Asymmetric synthesis of (?)-Aplysillamide B
1999
·
Stephen G. Davies
, Hitesh J. Sanganee
, et al.
·
Tetrahedron
·
71
A Practical Procedure for the Multigram Synthesis of the SuperQuat Chiral Auxiliaries
1998
·
Steven D. Bull
, Stephen G. Davies
, et al.
·
Synlett
·
69
One-pot nitro-Mannich/hydroamination cascades for the direct synthesis of 2,5-disubstituted pyrroles using base and gold catalysis
2011
·
David M. Barber
, Hitesh Sanganee
, et al.
·
Chemical Communications
·
61
Genetic architecture of telomere length in 462,666 UK Biobank whole-genome sequences
2024
·
Oliver S. Burren
, Ryan S. Dhindsa
, et al.
·
Nature Genetics
·
58
PDF
Pioneering government-sponsored drug repositioning collaborations: progress and learning
2015
·
Donald E. Frail
, Madeleine Brady
, et al.
·
Nature Reviews Drug Discovery
·
57
One-Pot Asymmetric Nitro-Mannich/Hydroamination Cascades for the Synthesis of Pyrrolidine Derivatives: Combining Organocatalysis and Gold Catalysis
2014
·
David M. Barber
, Andrej Ďuriš
, et al.
·
ACS Catalysis
·
55
PDF
Cathepsin C Inhibitors: Property Optimization and Identification of a Clinical Candidate
2014
·
Mark Furber
, Anna-Karin Tiden
, et al.
·
Journal of Medicinal Chemistry
·
54
SuperQuat N-acyl-5,5-dimethyloxazolidin-2-ones for the asymmetric synthesis of α-alkyl and β-alkyl aldehydes
2003
·
Steven D. Bull
, Stephen G. Davies
, et al.
·
Organic & Biomolecular Chemistry
·
54
Discovery of potent CRTh2 (DP2) receptor antagonists
2006
·
Timothy N. Birkinshaw
, Simon J. Teague
, et al.
·
Bioorganic & Medicinal Chemistry Letters
·
42
SuperQuat, (S)-4-benzyl-5,5-dimethyl-oxazolidin-2-one for the asymmetric synthesis of α-substituted-aldehydes
2000
·
Steven D Bull
, Stephen G Davies
, et al.
·
Tetrahedron Asymmetry
·
42
Potent Dual Inhibitors of TORC1 and TORC2 Complexes (KU-0063794 and KU-0068650) Demonstrate In Vitro and Ex Vivo Anti-Keloid Scar Activity
2013
·
Farhatullah Syed
, Hitesh J. Sanganee
, et al.
·
Journal of Investigative Dermatology
·
38
Substituted indole-1-acetic acids as potent and selective CRTh2 antagonists—discovery of AZD1981
2011
·
Tim Luker
, Roger Bonnert
, et al.
·
Bioorganic & Medicinal Chemistry Letters
·
38
Synthesis and utility of the 3,3-dimethyl-5-substituted-2-pyrrolidinone ‘Quat’ chiral auxiliary
2002
·
Stephen G. Davies
, Darren J. Dixon
, et al.
·
Tetrahedron Asymmetry
·
37
Asymmetric aldol and alkylation reactions mediated by the “quat” chiral auxiliary (R)-(−)-5-methyl-3,3-dimethyl-2-pyrrolidinone
1994
·
Stephen G. Davies
, Gilles J.-M. Doisneau
, et al.
·
Tetrahedron Letters
·
37
Synthesis of 5-substituted-3,3-dimethyl-2-pyrrolidinones: “quat” chiral auxiliaries
1994
·
Stephen G. Davies
, Gilles J.-M. Doisneau
, et al.
·
Tetrahedron Letters
·
35
Activation of the Wnt Pathway through AR79, a GSK3β Inhibitor, Promotes Prostate Cancer Growth in Soft Tissue and Bone
2013
·
Yuan Jiang
, Jinlu Dai
, et al.
·
Molecular Cancer Research
·
32
Stereoselective functionalisation of SuperQuat enamides: asymmetric synthesis of homochiral 1,2-diols and α-benzyloxy carbonyl compounds
2008
·
Caroline Aciro
, Stephen G. Davies
, et al.
·
Tetrahedron
·
31
Discovery of small molecule human C5a receptor antagonists
2009
·
Hitesh J. Sanganee
, Andrew Baxter
, et al.
·
Bioorganic & Medicinal Chemistry Letters
·
27
Oxidative Functionalisation of SuperQuat Enamides: Asymmetric Synthesis of Homochiral 1,2 Diols
2003
·
Stephen G. Davies
, Min-Suk Key
, et al.
·
Synlett
·
27
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Works count:
95
Citation count:
1,877
H-index:
26
I10-index:
35
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