Beeraiah Baire - Publications

2013- IIT Madras 
Organic chemistry, natural products chemistry

63 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
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  0.774
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  0.803
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  0.798
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  0.788
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  0.609
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  0.798
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  0.632
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  0.778
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  0.793
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  0.754
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  0.812
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  0.802
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  0.769
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  0.804
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  0.765
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  0.771
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  0.795
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  0.635
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  0.779
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  0.808
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  0.754
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  0.603
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  0.605
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  0.763
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  0.614
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  0.817
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  0.737
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  0.763
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  0.775
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  0.531
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  0.78
2017 Chinta BS, Baire B. Formal total synthesis of selaginpulvilin D. Organic & Biomolecular Chemistry. 15: 5908-5911. PMID 28534921 DOI: 10.1039/c7ob00950j  0.76
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  0.755
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  0.593
2017 Santhi J, Baire B. Carbonyl Directed Regioselective Hydration of Alkynes under Ag-Catalysis Chemistryselect. 2: 4338-4342. DOI: 10.1002/SLCT.201700665  0.778
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  0.786
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  0.741
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  0.744
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  0.593
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  0.814
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  0.812
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  0.716
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  0.761
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  0.77
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  0.764
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  0.782
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  0.801
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  0.505
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  0.746
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  0.623
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  0.515
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  0.789
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  0.808
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  0.799
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