| 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 |
0.805 |
|
| 2024 |
Khan S, Baire B. BiX-Mediated Hydrohalogenations of HDDA Benzynes: An Approach to Polycyclic Aryl Halides. Organic Letters. 26: 8165-8170. PMID 39292185 DOI: 10.1021/acs.orglett.4c03061 |
0.785 |
|
| 2024 |
Bommanaboina B, Roy D, Baire B. Integrated synthesis of 3,4-carbazoquinone alkaloids -Me-carbazoquinocin A, B and D-F. Rsc Advances. 14: 27372-27384. PMID 39205936 DOI: 10.1039/d4ra05347h |
0.796 |
|
| 2023 |
Baire B, Gandhi S, Bommanaboina B, Roy D. The Bis(indolylmethyl) ethers: Design, Prototypical Synthesis, and Scope Studies. The Journal of Organic Chemistry. 88: 12115-12120. PMID 37537963 DOI: 10.1021/acs.joc.3c01116 |
0.777 |
|
| 2023 |
Roy D, Baire B. Diastereoselective Biomimetic Synthesis of Dimeric Tetrahydrocarbazoles via a Copper(II)-Catalyzed Cycloisomerization-[3+2] Cyclodimerization Cascade. Angewandte Chemie (International Ed. in English). e202304557. PMID 37134297 DOI: 10.1002/anie.202304557 |
0.806 |
|
| 2022 |
Roy D, Tharra P, Baire B. An approach to functionalized carbazoles from -enoate propargylic alcohols. A unified total synthesis of -Me-carazostatin, -Me-carbazoquinocin C and -Me-lipocarbazole A4. Chemical Communications (Cambridge, England). 58: 10210-10213. PMID 36000534 DOI: 10.1039/d2cc03526j |
0.8 |
|
| 2022 |
Yadav B, Baire B. Ag(I)-Promoted, Diastereoselective Cyclo-isomerization of -Alkynyl-7-azaindole-2-carbinols. Selective Synthesis of -1,2-Diarylpyrrolo[1,2-]indol-3-ones and ()-8-Benzylideneoxazolo[3',4'':1,5]pyrrolo[2,3-]pyridines. Organic Letters. 24: 5450-5455. PMID 35834489 DOI: 10.1021/acs.orglett.2c02179 |
0.622 |
|
| 2022 |
Mishra S, Nair SR, Baire B. Recent approaches for the synthesis of pyridines and (iso)quinolines using propargylic Alcohols. Organic & Biomolecular Chemistry. PMID 35678139 DOI: 10.1039/d2ob00587e |
0.792 |
|
| 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 |
0.607 |
|
| 2021 |
Baire B, Santhi J. Ag(I)-Promoted homo-dimerization of 2-(alk-2-yn-1-onyl)-1-alkynylbenzenes a [4 + 2] cycloaddition of benzopyrylium ions: access to structurally unique naphthalenes. Organic & Biomolecular Chemistry. 20: 247-251. PMID 34904139 DOI: 10.1039/d1ob02229f |
0.799 |
|
| 2021 |
Baire B, Yadav B. TfOH catalysed domino-double annulation of arenes with propargylic alcohols: a unified approach to indene polycyclic systems. Chemical Communications (Cambridge, England). 57: 12796-12799. PMID 34782905 DOI: 10.1039/d1cc05253e |
0.63 |
|
| 2021 |
Roy D, Tharra P, Baire B. An Approach for the Generation of γ-Propenylidene-γ-butenolides and Application to the Total Synthesis of Rubrolides. Organic Letters. PMID 34259007 DOI: 10.1021/acs.orglett.1c01529 |
0.781 |
|
| 2021 |
Khan S, Baire B. Fe-Catalysed Coupling Reactions Between Alkynes and Alcohols. Chemical Record (New York, N.Y.). PMID 34105249 DOI: 10.1002/tcr.202100130 |
0.789 |
|
| 2021 |
Nair SR, Baire B. Recent Dearomatization Strategies of Benzofurans and Benzothiophenes Asian Journal of Organic Chemistry. 10: 932-948. DOI: 10.1002/AJOC.202100025 |
0.757 |
|
| 2020 |
Baire B, Roy D. Evidence for atropisomerism in polycyclic γ-butenolides. Synthesis, scope and spectroscopic studies. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 33378093 DOI: 10.1002/chem.202005174 |
0.813 |
|
| 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 |
0.81 |
|
| 2020 |
Santhi J, Baire B. One‐pot, Direct Synthesis of 3‐Hydroxy‐3‐aryl‐1‐indanones and their 2‐Benzylidene Derivatives from 2‐Alkynylbenzophenones Chemistryselect. 5: 8151-8156. DOI: 10.1002/slct.202001104 |
0.803 |
|
| 2020 |
Gandhi S, Sivadas V, Baire B. Thiourea–Tertiary Amine Promoted Cascade Catalysis: A Tool for Complexity Generation European Journal of Organic Chemistry. 2021: 220-234. DOI: 10.1002/EJOC.202001114 |
0.77 |
|
| 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 |
0.805 |
|
| 2020 |
Gandhi S, Baire B. Fe(III)‐Catalyzed, Cyclizative Coupling between 2‐Alkynylbenzoates and Carbinols: Rapid Generation of Polycyclic Isocoumarins and Phthalides and Mechanistic Study Advanced Synthesis & Catalysis. 362: 2651-2657. DOI: 10.1002/adsc.202000313 |
0.766 |
|
| 2019 |
Debsharma K, Santhi J, Baire B, Prasad E. Aggregation-Induced Emission Active Donor-Acceptor Fluorophore as a Dual Sensor for Volatile Acids and Aromatic Amines. Acs Applied Materials & Interfaces. PMID 31790187 DOI: 10.1021/Acsami.9B17988 |
0.772 |
|
| 2019 |
Santhi J, Baire B. An Unusual Conversion of 2-(Alkynonyl)Alkynylbenzenes to Isocoumarins by a Retro-Favorskii-like Degradation. Chemistry, An Asian Journal. 14: 3161-3165. PMID 31355983 DOI: 10.1002/asia.201900745 |
0.798 |
|
| 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 |
0.636 |
|
| 2019 |
Chinta BS, Gandhi S, Baire B. Acid catalysed rearrangement of isobenzofurans to angularly fused phthalides. Organic & Biomolecular Chemistry. PMID 31032835 DOI: 10.1039/c9ob00708c |
0.782 |
|
| 2019 |
Jeyakumar M, Sathya S, Gandhi S, Tharra P, Suryanarayanan V, Singh SK, Baire B, Pandima Devi K. α-bisabolol β-D-fucopyranoside as a potential modulator of β-amyloid peptide induced neurotoxicity: An in vitro &in silico study. Bioorganic Chemistry. 88: 102935. PMID 31030060 DOI: 10.1016/j.bioorg.2019.102935 |
0.748 |
|
| 2019 |
Gandhi S, Baire B. Unusual formation of Cyclopenta[b]indoles from 3-Indolylmethanols and Alkynes. The Journal of Organic Chemistry. PMID 30852894 DOI: 10.1021/acs.joc.8b03027 |
0.811 |
|
| 2019 |
Chinta BS, Santhi J, Baire B. First Approach for Structurally Unique Thieno[2,3‐
e
] isobenzofuran‐8(6
H
)‐one Tricyclic Framework of Echinothiophene and Echinothiophenegenol Chemistryselect. 4: 9811-9813. DOI: 10.1002/slct.201902452 |
0.755 |
|
| 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 |
0.604 |
|
| 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 |
0.606 |
|
| 2018 |
Chinta BS, Sanapa H, Vasikarla KP, Baire B. Highly regioselective, electrophile induced cyclizations of 2-(prop-1-ynyl)benzamides. Organic & Biomolecular Chemistry. 16: 3947-3951. PMID 29745950 DOI: 10.1039/c8ob00434j |
0.761 |
|
| 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 |
0.612 |
|
| 2018 |
Tharra P, Baire B. Regioselective Cyclization of (Indol-3-yl)pentyn-3-ols as an Approach to (Tetrahydro)carbazoles. Organic Letters. 20: 1118-1121. PMID 29381074 DOI: 10.1021/acs.orglett.8b00042 |
0.818 |
|
| 2018 |
Chinta BS, Baire B. Total synthesis of selaginpulvilins A and C. Organic & Biomolecular Chemistry. 16: 262-265. PMID 29239444 DOI: 10.1039/c7ob02609a |
0.769 |
|
| 2018 |
Chinta BS, Sanapa H, Vasikarla KP, Baire B. Synthetic approach to seco-tetracenomycin natural products saccharothrixone A–C Tetrahedron Letters. 59: 1970-1973. DOI: 10.1016/J.TETLET.2018.04.031 |
0.734 |
|
| 2018 |
Gandhi S, Baire B. Calcium(II) Catalyzed Cycloisomerization of cis
-6-Hydroxy/(Acyloxy)hex-2-en-4-ynals to 2-Acyl- and 2-(Acyloxyalkenyl)furans Chemistryselect. 3: 4490-4494. DOI: 10.1002/SLCT.201800618 |
0.765 |
|
| 2018 |
Roy D, Tharra P, Baire B. Intercepted Meyer-Schuster Rearrangements in Organic Synthesis Asian Journal of Organic Chemistry. 7: 1015-1032. DOI: 10.1002/AJOC.201800089 |
0.776 |
|
| 2017 |
Ross SP, Baire B, Hoye TR. Mechanistic Duality in Tertiary Amine Additions to Thermally Generated Hexadehydro-Diels-Alder Benzynes. Organic Letters. PMID 28981290 DOI: 10.1021/Acs.Orglett.7B02888 |
0.529 |
|
| 2017 |
Tharra P, Baire B. A coherent study on the Z-enoate assisted Meyer-Schuster rearrangement. Organic & Biomolecular Chemistry. 15: 5579-5584. PMID 28639639 DOI: 10.1039/c7ob01221g |
0.782 |
|
| 2017 |
Chinta BS, Baire B. Formal total synthesis of selaginpulvilin D. Organic & Biomolecular Chemistry. 15: 5908-5911. PMID 28534921 DOI: 10.1039/c7ob00950j |
0.759 |
|
| 2017 |
Tharra P, Baire B. Unconventional Reactivity of (Z)-Enoate Propargylic Alcohols in the Presence of Acids. Chemistry (Weinheim An Der Bergstrasse, Germany). 23: 2014-2017. PMID 27935194 DOI: 10.1002/chem.201605654 |
0.814 |
|
| 2017 |
Chinta BS, Siraswar A, Baire B. The dehydro Diels-Alder (DDA) reaction based approach to isofuranonaphthalenone, nodulones A-C and xestolactone A Tetrahedron. 73: 4178-4185. DOI: 10.1016/J.TET.2016.11.015 |
0.754 |
|
| 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 |
0.589 |
|
| 2017 |
Santhi J, Baire B. Carbonyl Directed Regioselective Hydration of Alkynes under Ag-Catalysis Chemistryselect. 2: 4338-4342. DOI: 10.1002/SLCT.201700665 |
0.779 |
|
| 2017 |
Gandhi S, Baire B. Ag(I) Catalyzed Cascade Approach to 2-(α-Hydroxyacyl)pyrroles Chemistryselect. 2: 3964-3968. DOI: 10.1002/SLCT.201700514 |
0.789 |
|
| 2017 |
Gandhi S, Tharra P, Baire B. Ag(I)-Catalyzed Cyclizative Hydration of Alkynes and Propargylic Alcohols. A Mild Approach to 2-Acylfuran Derivatives Chemistryselect. 2: 1058-1062. DOI: 10.1002/SLCT.201601623 |
0.787 |
|
| 2017 |
Chinta BS, Baire B. On the Distribution of Linear versus Angular Naphthalenes in Aromatic Tetradehydro-Diels-Alder Reactions - Effect of Linker Structure and Steric Bulk European Journal of Organic Chemistry. 2017: 3381-3385. DOI: 10.1002/EJOC.201700588 |
0.739 |
|
| 2017 |
Chinta BS, Baire B. First Synthesis of the [5-5-6-6] Tetracyclic Framework of Spiropreussione B European Journal of Organic Chemistry. 2017: 3457-3460. DOI: 10.1002/EJOC.201700464 |
0.742 |
|
| 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 |
0.591 |
|
| 2016 |
Tharra P, Baire B. Regioselective, cascade [3+2] annulation of β-naphthols (resorcinols) with Z-enoate propargylic alcohols: a novel entry for the synthesis of complex naphtho(benzo)furans. Chemical Communications (Cambridge, England). 52: 14290-14293. PMID 27882364 DOI: 10.1039/c6cc08126f |
0.815 |
|
| 2016 |
Tharra P, Baire B. The Z-enoate assisted, Meyer-Schuster rearrangement cascade: unconventional synthesis of α-arylenone esters. Chemical Communications (Cambridge, England). 52: 12147-12150. PMID 27711450 DOI: 10.1039/c6cc06639a |
0.813 |
|
| 2016 |
Chinta BS, Baire B. A systematic study on the Cadiot–Chodkiewicz cross coupling reaction for the selective and efficient synthesis of hetero-diynes Rsc Advances. 6: 54449-54455. DOI: 10.1039/C6RA07308E |
0.762 |
|
| 2016 |
Chinta BS, Baire B. Catalyst free, three-component approach for unsymmetrical triarylmethanes (TRAMs) Tetrahedron Letters. 57: 5381-5384. DOI: 10.1016/J.TETLET.2016.10.087 |
0.712 |
|
| 2016 |
Chinta BS, Baire B. Reactivity of indole-3-alkoxides in the absence of acids: Rapid synthesis of homo-bisindolylmethanes Tetrahedron. 72: 8106-8116. DOI: 10.1016/J.TET.2016.10.067 |
0.759 |
|
| 2016 |
Chinta BS, Baire B. ChemInform Abstract: A Systematic Study on the Cadiot-Chodkiewicz Cross Coupling Reaction for the Selective and Efficient Synthesis of Hetero-diynes. Cheminform. 47. DOI: 10.1002/CHIN.201642061 |
0.769 |
|
| 2016 |
Santhi J, Baire B. N-Iodosuccinimide-Promoted Rapid Access to Indeno[1,2-c]pyrrolesvia[3+2] Annulation of Enamine-alkynes Advanced Synthesis & Catalysis. 358: 3817-3823. DOI: 10.1002/ADSC.201600711 |
0.765 |
|
| 2015 |
Chinta BS, Baire B. Stereoselective, Cascade Synthesis of trans-Enynones through Coupling-Isomerization Reaction. The Journal of Organic Chemistry. 80: 10208-17. PMID 26394546 DOI: 10.1021/acs.joc.5b01780 |
0.781 |
|
| 2015 |
Tharra P, Baire B. Mild Approach to 2-Acylfurans via Intercepted Meyer-Schuster Rearrangement of 6-Hydroxyhex-2-en-4-ynals. The Journal of Organic Chemistry. 80: 8314-28. PMID 26200129 DOI: 10.1021/acs.joc.5b01420 |
0.803 |
|
| 2015 |
Nguyen QL, Baire B, Hoye TR. Competition between classical and hexadehydro-Diels-Alder (HDDA) reactions of HDDA triynes with furan. Tetrahedron Letters. 56: 3265-3267. PMID 26028780 DOI: 10.1016/J.Tetlet.2014.12.053 |
0.508 |
|
| 2014 |
Hoye TR, Baire B, Wang T. Tactics for Probing Aryne Reactivity: Mechanistic Studies of Silicon-oxygen Bond Cleavage During the Trapping of (HDDA-generated) Benzynes by Silyl Ethers. Chemical Science (Royal Society of Chemistry : 2010). 5: 545-550. PMID 25419449 DOI: 10.1039/C3Sc53014K |
0.52 |
|
| 2014 |
Woods BP, Baire B, Hoye TR. Rates of hexadehydro-Diels-Alder (HDDA) cyclizations: impact of the linker structure. Organic Letters. 16: 4578-81. PMID 25153729 DOI: 10.1021/Ol502131R |
0.734 |
|
| 2014 |
Chen J, Baire B, Hoye TR. CYCLOADDITION REACTIONS OF AZIDE, FURAN, AND PYRROLE UNITS WITH BENZYNES GENERATED BY THE HEXADEHYDRO-DIELS-ALDER (HDDA) REACTION. Heterocycles. 88: 1191-1200. PMID 24910496 DOI: 10.3987/Com-13-S(S)83 |
0.523 |
|
| 2014 |
Hassig CA, Zeng FY, Kung P, Kiankarimi M, Kim S, Diaz PW, Zhai D, Welsh K, Morshedian S, Su Y, O'Keefe B, Newman DJ, Rusman Y, Kaur H, Salomon CE, ... ... Baire B, et al. Ultra-High-Throughput Screening of Natural Product Extracts to Identify Proapoptotic Inhibitors of Bcl-2 Family Proteins. Journal of Biomolecular Screening. 19: 1201-1211. PMID 24870016 DOI: 10.1177/1087057114536227 |
0.618 |
|
| 2014 |
Hoye TR, Chen J, Baire B. ChemInform Abstract: Cycloaddition Reactions of Azide, Furan, and Pyrrole Units with Benzynes Generated by the Hexadehydro-Diels-Alder (HDDA) Reaction. Cheminform. 45: no-no. DOI: 10.1002/chin.201423123 |
0.519 |
|
| 2013 |
Niu D, Willoughby PH, Woods BP, Baire B, Hoye TR. Alkane desaturation by concerted double hydrogen atom transfer to benzyne. Nature. 501: 531-4. PMID 24067712 DOI: 10.1038/Nature12492 |
0.793 |
|
| 2013 |
Baire B, Niu D, Willoughby PH, Woods BP, Hoye TR. Synthesis of complex benzenoids via the intermediate generation of o-benzynes through the hexadehydro-Diels-Alder reaction. Nature Protocols. 8: 501-8. PMID 23411632 DOI: 10.1038/Nprot.2013.017 |
0.812 |
|
| 2012 |
Hoye TR, Baire B, Niu D, Willoughby PH, Woods BP. The hexadehydro-Diels-Alder reaction. Nature. 490: 208-12. PMID 23060191 DOI: 10.1038/Nature11518 |
0.803 |
|
| Show low-probability matches. |