Year |
Citation |
Score |
2025 |
Nair SR, Sadhukhan S, Baire B. Intramolecular Halogenative-Arylation of Alkynes Using -halosuccinimide (NXS) Reagents in the CHCN-HO System. The Journal of Organic Chemistry. 90: 2230-2244. PMID 39895646 DOI: 10.1021/acs.joc.4c02598 |
0.617 |
|
2022 |
Sadhukhan S, Baire B. Tunable Lewis Basicity and Nucleophilicity of Water against α,α-Dihalo-β-acetoxyketones for the Selective Synthesis of α-Haloenones and 1,2-Diketones. The Journal of Organic Chemistry. PMID 35394788 DOI: 10.1021/acs.joc.1c02780 |
0.727 |
|
2020 |
Sadhukhan S, Santhi J, Baire B. The α,α-Dihalocarbonyl Building Blocks: An Avenue for New Reaction Development in Organic Synthesis. Chemistry (Weinheim An Der Bergstrasse, Germany). 26: 7145-7175. PMID 31916618 DOI: 10.1002/chem.201905475 |
0.722 |
|
2020 |
Sadhukhan S, Santhi J, Baire B. Frontispiece: The α,α‐Dihalocarbonyl Building Blocks: An Avenue for New Reaction Development in Organic Synthesis Chemistry – a European Journal. 26. DOI: 10.1002/chem.202083261 |
0.711 |
|
2019 |
Sadhukhan S, Baire B. Formal Halo-Meyer-Schuster Rearrangement of Propargylic Acetates through a Novel Intermediate and an Unexampled Mechanistic Pathway. Chemistry (Weinheim An Der Bergstrasse, Germany). 25: 9816-9820. PMID 31141230 DOI: 10.1002/chem.201901856 |
0.757 |
|
2019 |
Sadhukhan S, Baire B. Metal Free Synthesis of α‐Acetoxy/Hydroxymethyl Ketones from Propargylic acetates Chemistryselect. 4: 3376-3380. DOI: 10.1002/SLCT.201900786 |
0.615 |
|
2019 |
Sadhukhan S, Baire B. Front Cover: Formal Halo‐Meyer–Schuster Rearrangement of Propargylic Acetates through a Novel Intermediate and an Unexampled Mechanistic Pathway (Chem. Eur. J. 42/2019) Chemistry – a European Journal. 25: 9780-9780. DOI: 10.1002/chem.201902920 |
0.611 |
|
2018 |
Sadhukhan S, Baire B. An Unprecedented (Semi)Favorskii Rearrangement. Evidence for the 2-(Acyloxy)cyclopropanones. Organic Letters. 20: 1748-1751. PMID 29577730 DOI: 10.1021/acs.orglett.8b00218 |
0.725 |
|
2017 |
Sadhukhan S, Baire B. An Expeditious Approach to α,α-Dihalo-α′-acetoxyketones from Propargylic Acetates Chemistryselect. 2: 8500-8503. DOI: 10.1002/SLCT.201701398 |
0.706 |
|
2017 |
Sadhukhan S, Baire B. Lewis Basicity of Water for a Selective Monodehalogenation of α,α-Dihalo Ketones to α-Halo Ketones and Mechanistic Study Advanced Synthesis & Catalysis. 360: 298-304. DOI: 10.1002/ADSC.201701233 |
0.717 |
|
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