Year |
Citation |
Score |
2023 |
Basha KS, Balamurugan R. Gold(I)-Catalyzed Regioselective Hydroarylation of Propiolic Acid with Arylboronic Acids. Organic Letters. 25: 4803-4807. PMID 37353304 DOI: 10.1021/acs.orglett.3c01492 |
0.792 |
|
2023 |
Reddy YP, Srinivasadesikan V, Balamurugan R, Lin MC, Anwar S. Synthesis of tetrahydrochromenes and dihydronaphthofurans a cascade process of [3 + 3] and [3 + 2] annulation reactions: mechanistic insight for 6- and 5- cyclisation. Rsc Advances. 13: 5796-5803. PMID 36816068 DOI: 10.1039/d2ra08163f |
0.414 |
|
2023 |
Mandal M, Pradhan R, Lourderaj U, Balamurugan R. Dodging the Conventional Reactivity of -Alkynylanilines under Gold Catalysis for Distal 7-- Cyclization. The Journal of Organic Chemistry. 88: 2260-2287. PMID 36744758 DOI: 10.1021/acs.joc.2c02668 |
0.67 |
|
2022 |
Ramesh G, Srivardhan V, Balamurugan R. Ag(I)-catalyzed cyclization of -alkynylacetophenones facilitated through acetal formation: synthesis of C3-naphthyl indole derivatives. Organic & Biomolecular Chemistry. PMID 36416470 DOI: 10.1039/d2ob01873j |
0.818 |
|
2022 |
Mandal M, Balamurugan R. TfOH-promoted synthesis of indoles and benzofurans involving cyclative transposition of vinyl ketone. Chemical Communications (Cambridge, England). 58: 9778-9781. PMID 35969016 DOI: 10.1039/d2cc03730k |
0.674 |
|
2022 |
Ramesh G, Ramulu BV, Balamurugan R. Activation of -Propargyl Alcohol Benzaldehydes under Acetalization Conditions for Intramolecular Electrophile Intercepted Meyer-Schuster Rearrangement. The Journal of Organic Chemistry. PMID 35687605 DOI: 10.1021/acs.joc.2c00826 |
0.794 |
|
2021 |
Ramesh G, Balamurugan R. Triflic Acid-Catalyzed Synthesis of Indole-Substituted Indane Derivatives via Formed Acetal-Facilitated Nucleophilic Addition and 4π-Electron-5-Carbon Electrocyclization Sequence. The Journal of Organic Chemistry. 86: 16278-16292. PMID 34762435 DOI: 10.1021/acs.joc.1c01396 |
0.831 |
|
2021 |
Tarigopula C, Manojveer S, Balamurugan R. Synthesis of Highly Substituted Biaryls by the Construction of a Benzene Ring via Formed Acetals. The Journal of Organic Chemistry. 86: 11871-11883. PMID 34425048 DOI: 10.1021/acs.joc.1c01277 |
0.831 |
|
2020 |
Mandal M, Sakthivel S, Balamurugan R. Brønsted/Lewis Acid-Promoted Site-Selective Intramolecular Cycloisomerizations of Aryl-Fused 1,6-Diyn-3-ones for Diversity-Oriented Synthesis of Benzo-Fused Fluorenes and Fluorenones and Naphthyl Ketones. The Journal of Organic Chemistry. PMID 33253563 DOI: 10.1021/acs.joc.0c02131 |
0.698 |
|
2020 |
Qin X, Thota GK, Singh R, Balamurugan R, Goycoolea FM. Synthetic homoserine lactone analogues as antagonists of bacterial quorum sensing. Bioorganic Chemistry. 98: 103698. PMID 32217369 DOI: 10.1016/J.Bioorg.2020.103698 |
0.761 |
|
2018 |
Sakthivel S, Balamurugan R. Annulation of a Highly Functionalized Diazo Building Block with Indoles Under Sc(OTf)3/Rh2(OAc)4 Multicatalysis Through Michael Addition/Cyclization Sequence. The Journal of Organic Chemistry. PMID 30178678 DOI: 10.1021/Acs.Joc.8B02127 |
0.46 |
|
2018 |
Mandal M, Balamurugan R. Triflic acid-Mediated Expedient Synthesis of Benzo[a
]fluorenes and Fluorescent Benzo[a
]fluorenones Advanced Synthesis & Catalysis. 360: 1453-1465. DOI: 10.1002/Adsc.201701516 |
0.651 |
|
2017 |
Naveen N, Balamurugan R. Catalyst free synthesis of α-fluoro-β-hydroxy ketones/α-fluoro-ynols via electrophilic fluorination of tertiary propargyl alcohols using Selectfluor™ (F-TEDA-BF4). Organic & Biomolecular Chemistry. 15: 2063-2072. PMID 28210740 DOI: 10.1039/C7Ob00140A |
0.791 |
|
2017 |
Koppolu SR, Balamurugan R. In situ formed acetals facilitated direct Michael addition of unactivated ketones New Journal of Chemistry. 41: 1186-1192. DOI: 10.1039/C6Nj02954J |
0.833 |
|
2017 |
Kumar Thota G, Tamilarasan D, Balamurugan R. Synthesis of Highly Functionalized Pyrrolidine Derivatives from Easily Accessible Diethyl (E
)-4-Oxohex-2-enedioate European Journal of Organic Chemistry. 2017: 6417-6426. DOI: 10.1002/Ejoc.201700997 |
0.467 |
|
2017 |
Sakthivel S, Sharma A, Balamurugan R. Silver-Catalyzed Synthesis of Substituted Pyridine Derivatives from N
-Propargylic α-Enamino Esters European Journal of Organic Chemistry. 2017: 3941-3946. DOI: 10.1002/Ejoc.201700559 |
0.477 |
|
2016 |
Das SN, Wagenknecht M, Nareddy PK, Bhuvanachandra B, Niddana R, Balamurugan R, Swamy MJ, Moerschbacher BM, Podile AR. Amino groups of chitosan are crucial for binding to a family 32 carbohydrate binding module of a chitosanase from Paenibacillus elgii. The Journal of Biological Chemistry. PMID 27405759 DOI: 10.1074/Jbc.M116.721332 |
0.738 |
|
2016 |
Sakthivel S, Kothapalli RB, Balamurugan R. The directing group wins over acidity: kinetically controlled regioselective lithiation for functionalization of 2-(2,4-dihalophenyl)-1,3-dithiane derivatives. Organic & Biomolecular Chemistry. 14: 1670-9. PMID 26699693 DOI: 10.1039/C5Ob02172C |
0.804 |
|
2016 |
Tarigopula C, Thota GK, Balamurugan R. Efficient Synthesis of Functionalized β-Keto Esters and β-Diketones through Regioselective Hydration of Alkynyl Esters and Alkynyl Ketones by Use of a Cationic NHC-AuICatalyst European Journal of Organic Chemistry. 2016: 5855-5861. DOI: 10.1002/Ejoc.201601025 |
0.802 |
|
2015 |
Manojveer S, Balamurugan R. In Situ Formed Acetal-Facilitated Synthesis of Substituted Indene Derivatives from o-Alkenylbenzaldehydes. Organic Letters. 17: 3600-3. PMID 26151291 DOI: 10.1021/Acs.Orglett.5B01695 |
0.814 |
|
2015 |
Koppolu SR, Niddana R, Balamurugan R. Gold-catalysed glycosylation reaction using an easily accessible leaving group. Organic & Biomolecular Chemistry. 13: 5094-7. PMID 25858173 DOI: 10.1039/C5Ob00248F |
0.796 |
|
2015 |
Thota GK, Tarigopula C, Balamurugan R. Tandem activation by gold: synthesis of dioxolanes by intermolecular reaction of epoxides and alkynes in acetone Tetrahedron. 71: 2280-2289. DOI: 10.1016/J.Tet.2015.02.040 |
0.821 |
|
2015 |
Manojveer S, Balamurugan R. A Cascade Approach to Naphthalene Derivatives fromo-Alkynylbenzaldehydes and Enolizable Ketones via in-situ-Formed Acetals European Journal of Organic Chemistry. 2015: 4254-4260. DOI: 10.1002/Ejoc.201500497 |
0.818 |
|
2015 |
Naveen N, Koppolu SR, Balamurugan R. Silver Hexafluoroantimonate-Catalyzed Direct α-Alkylation of Unactivated Ketones Advanced Synthesis & Catalysis. 357: 1463-1473. DOI: 10.1002/Adsc.201400870 |
0.789 |
|
2014 |
Manojveer S, Balamurugan R. A facile access to substituted benzo[a]fluorenes from o-alkynylbenzaldehydes via in situ formed acetals. Chemical Communications (Cambridge, England). 50: 9925-8. PMID 25032517 DOI: 10.1039/C4Cc03934C |
0.838 |
|
2014 |
Koppolu SR, Naveen N, Balamurugan R. Triflic acid promoted direct α-alkylation of unactivated ketones using benzylic alcohols via in situ formed acetals. The Journal of Organic Chemistry. 79: 6069-78. PMID 24901388 DOI: 10.1021/Jo500759A |
0.805 |
|
2014 |
Manojveer S, Balamurugan R. Synthesis of naphthalene derivatives from ortho-alkynylacetophenone derivatives via tandem in situ incorporation of acetal and intramolecular heteroalkyne metathesis/annulation. Organic Letters. 16: 1712-5. PMID 24597947 DOI: 10.1021/Ol5003835 |
0.837 |
|
2014 |
Kothapalli RB, Niddana R, Balamurugan R. Synthesis of chiral α-diarylacetic esters by stereospecific 1,2-aryl migration promoted by in situ generated acetals from benzoins. Organic Letters. 16: 1278-81. PMID 24559219 DOI: 10.1021/Ol500292C |
0.772 |
|
2013 |
Gudla V, Balamurugan R. Synthesis of 1-arylnaphthalenes by gold-catalyzed one-pot sequential epoxide to carbonyl rearrangement and cyclization with arylalkynes. Chemistry, An Asian Journal. 8: 414-28. PMID 23184808 DOI: 10.1002/Asia.201200817 |
0.84 |
|
2012 |
Gudla V, Balamurugan R. AuCl3/AgSbF6-catalyzed rapid epoxide to carbonyl rearrangement Tetrahedron Letters. 53: 5243-5247. DOI: 10.1016/J.Tetlet.2012.07.056 |
0.804 |
|
2011 |
Gudla V, Balamurugan R. Synthesis of arylnaphthalene lignan scaffold by gold-catalyzed intramolecular sequential electrophilic addition and benzannulation. The Journal of Organic Chemistry. 76: 9919-33. PMID 22029795 DOI: 10.1021/Jo201918D |
0.815 |
|
2011 |
Balamurugan R, Manojveer S. Gold/copper-catalyzed activation of the aci-form of nitromethane in the synthesis of methylene-bridged bis-1,3-dicarbonyl compounds. Chemical Communications (Cambridge, England). 47: 11143-5. PMID 21894337 DOI: 10.1039/C1Cc14926A |
0.789 |
|
2011 |
Balamurugan R, Naveen N, Manojveer S, Nama MV. Homo and Heterocoupling of Terminal Alkynes Using Catalytic CuCl2 and DBU Australian Journal of Chemistry. 64: 567. DOI: 10.1071/Ch11080 |
0.778 |
|
2011 |
Balamurugan R, Kothapalli RB, Thota GK. Gold-Catalysed Activation of Epoxides: Application in the Synthesis of Bicyclic Ketals European Journal of Organic Chemistry. 2011: 1557-1569. DOI: 10.1002/Ejoc.201001214 |
0.792 |
|
2010 |
Dekker FJ, Rocks O, Vartak N, Menninger S, Hedberg C, Balamurugan R, Wetzel S, Renner S, Gerauer M, Schölermann B, Rusch M, Kramer JW, Rauh D, Coates GW, Brunsveld L, et al. Small-molecule inhibition of APT1 affects Ras localization and signaling. Nature Chemical Biology. 6: 449-56. PMID 20418879 DOI: 10.1038/Nchembio.362 |
0.601 |
|
2009 |
Balamurugan R, Gudla V. Gold-catalyzed electrophilic addition to arylalkynes. A facile method for the regioselective synthesis of substituted naphthalenes. Organic Letters. 11: 3116-9. PMID 19534473 DOI: 10.1021/Ol900863D |
0.827 |
|
2009 |
Reddy BG, Silk JD, Salio M, Balamurugan R, Shepherd D, Ritter G, Cerundolo V, Schmidt RR. Nonglycosidic agonists of invariant NKT cells for use as vaccine adjuvants. Chemmedchem. 4: 171-5. PMID 19160440 DOI: 10.1002/Cmdc.200800354 |
0.39 |
|
2009 |
Balamurugan R, Koppolu SR. Scope of AuCl3 in the activation of per-O-acetylglycals Tetrahedron. 65: 8139-8142. DOI: 10.1016/J.Tet.2009.07.087 |
0.774 |
|
2008 |
Wang Z, Gu C, Colby T, Shindo T, Balamurugan R, Waldmann H, Kaiser M, Van Der Hoorn RAL. β-Lactone probes identify a papain-like peptide ligase in Arabidopsis thaliana Nature Chemical Biology. 4: 557-563. PMID 18660805 DOI: 10.1038/Nchembio.104 |
0.402 |
|
2006 |
Yadav VK, Gupta A, Balamurugan R, Sriramurthy V, Kumar NV. Distinguishing the early and late transition states and exploring the validity of sigma --> sigma*#, sigma# --> sigma*, and sigma --> pi*(C=O) concepts in diastereoselection from NBO analysis. The Journal of Organic Chemistry. 71: 4178-82. PMID 16709058 DOI: 10.1021/Jo060291F |
0.594 |
|
2005 |
Balamurugan R, Dekker FJ, Waldmann H. Design of compound libraries based on natural product scaffolds and protein structure similarity clustering (PSSC). Molecular Biosystems. 1: 36-45. PMID 16880961 DOI: 10.1039/B503623B |
0.424 |
|
2004 |
Balamurugan R, Pachamuthu K, Schmidt RR. Michael-Type Addition to 2-Nitrogalactal - A Simple Method to Access 1,1-Linked Oligosaccharides Synlett. 2005: 134-138. DOI: 10.1055/S-2004-836059 |
0.505 |
|
2003 |
Yadav VK, Balamurugan R. Diastereoselective aldol reactions of enolates generated from vicinally substituted trimethylsilylmethyl cyclopropyl ketones. Organic Letters. 5: 4281-4. PMID 14601980 DOI: 10.1021/Ol035481G |
0.75 |
|
2003 |
Yadav VK, Babu K, Balamurugan R. Bicyclo[2.1.1]hexan-2-one as a new probe for the study of π-facial selectivity in nucleophilic additions. A comment Tetrahedron Letters. 44: 6617-6619. DOI: 10.1016/S0040-4039(03)01681-2 |
0.578 |
|
2002 |
Yadav VK, Balamurugan R. Synthesis of gamma-methylene oxacycles and alpha- and beta-alkylidene lactones via silicon-assisted ring opening of cyclopropyl carbinols. Chemical Communications (Cambridge, England). 514-5. PMID 12120567 DOI: 10.1039/B111332C |
0.613 |
|
2002 |
Yadav VK, Balamurugan R. 4-Oxatricyclo[5.2.1.0(2,6)]decan-10-one and 4-oxatricyclo[5.2.1.0(2,6)]dec-8-en-10-one. Experimental and DFT investigations of the pi-selectivities. The Journal of Organic Chemistry. 67: 587-90. PMID 11798335 DOI: 10.1021/Jo015945T |
0.584 |
|
2001 |
Parvez M, Yadav VK, Balamurugan R. pi-Facial selectivities of diastereotopic ketones: p-bromobenzoates of 4-hetero-1-decalinols. Acta Crystallographica. Section C, Crystal Structure Communications. 57: 1084-8. PMID 11588379 DOI: 10.1107/S0108270101009544 |
0.608 |
|
2001 |
Yadav VK, Balamurugan R. Silicon-assisted ring opening of donor-acceptor substituted cyclopropanes. An expedient entry to substituted dihydrofurans. Organic Letters. 3: 2717-9. PMID 11506617 DOI: 10.1021/Ol0163169 |
0.693 |
|
2001 |
Yadav VK, Balamurugan R, Parvez M, Yamdagni R. The thionophosphate–thiolophosphate photoisomerization proceeds predominantly through a non-chain radical pathway. Synthetically viable benzylation of tetrahydrofuran, propan-2-ol and olefins Journal of the Chemical Society-Perkin Transactions 1. 323-332. DOI: 10.1039/B003501G |
0.398 |
|
2000 |
Yadav VK, Jeyaraj DA, Balamurugan R. The Cation Complexation Model Predicts the Experimental π-Facial Selectivity of 2-ax- and 2-eq-Substituted Cyclohexanones. A Detailed Ab Initio MO Investigation Tetrahedron. 56: 7581-7589. DOI: 10.1016/S0040-4020(00)00663-3 |
0.588 |
|
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