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Benjamin F. Rahemtulla

Observed name: Rahemtulla, Benjamin F.
ORCID: 0000-0003-3702-0833
Observed ORCID: 0000-0003-3702-0833
OpenAlex ID: A5037344888
Catalytic Enantioselective Synthesis of C1‐ and C2‐Symmetric Spirobiindanones through Counterion‐Directed Enolate C‐Acylation
2016 · Benjamin F. Rahemtulla, Hugh F. Clark, et al. · Angewandte Chemie International Edition · 43
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Discovery of HC-7366: An Orally Bioavailable and Efficacious GCN2 Kinase Activator
2024 · Christopher G. Thomson, Thomas D. Aicher, et al. · Journal of Medicinal Chemistry · 18
Regioselective Synthesis of Fully Substituted Fused Pyrroles through an Oxidant-Free Multicomponent Reaction
2023 · Konstantinos Afratis, Joseph M. Bateman, et al. · Organic Letters · 12
Catalytic Enantioselective Synthesis of C1‐ and C2‐Symmetric Spirobiindanones through Counterion‐Directed Enolate C‐Acylation
2016 · Benjamin F. Rahemtulla, Hugh F. Clark, et al. · Angewandte Chemie · 7
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Access to Cyclic Aliphatic Sulfonyl Fluorides via Diels–Alder Cycloaddition
2025 · Christian J. Kuper, Delia Brustur, et al. · The Journal of Organic Chemistry · 3
Diastereoselective Synthesis of Morpholine Derivatives from Grignard Reagents and N-Sulfinyl Imines
2021 · Joseph M. Bateman, Diana Chan, et al. · Synlett · 1
Discovery of Potent, Orally Bioavailable, and CNS-Penetrant 1,2,3-Triazolopyridinyl Piperazine-Based PARP1-Selective Inhibitors
2026 · Tammy Ladduwahetty, Benjamin F. Rahemtulla, et al. · Journal of Medicinal Chemistry
Dicyclohexyl(2′,4′,6′‐triisopropyl‐3,6‐dimethoxy‐[1,1′‐biphenyl]‐2‐yl)phosphine; Di‐ tert ‐butyl(2′,4′,6′‐triisopropyl‐3,6‐dimethoxy‐[1,1′‐biphenyl]‐2‐yl)phosphine; and Diadamantan‐1‐yl(2′,4′,6′‐triisopropyl‐3,6‐dimethoxy‐[1,1′‐biphenyl]‐2‐yl)phosphine
2021 · Mustafa Moroglu, Joseph M. Bateman, et al. · Wiley eBooks
Development of cation-directed acylation reactions
2018 · Rahemtulla, Benjamin F. · Oxford University Research Archive (ORA) (University of Oxford)
CCDC 1486386: Experimental Crystal Structure Determination
2016 · Rahemtulla, Benjamin F., Clark, Hugh F., et al. · The Cambridge Structural Database
Works count: 10
Citation count: 84
H-index: 4
I10-index: 3
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