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Uttam Krishan Tambar, Ph.D. - Publications

Affiliations: 
2009- Chemistry University of Texas Southwestern Medical Center, Dallas, TX, United States 
Area:
Organic Chemistry
Website:
http://tambargroup.com/
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51 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 Manna MS, Yoo SY, Sharique M, Choi H, Pudasaini B, Baik MH, Tambar UK. Copper-Catalyzed Regiodivergent Internal Allylic Alkylations. Angewandte Chemie (International Ed. in English). e202304848. PMID 37327025 DOI: 10.1002/anie.202304848  0.336
2023 Vincent CA, Chiriac MI, Troian-Gautier L, Tambar UK. Photocatalytic Sulfonyl Fluorination of Alkyl Organoboron Substrates. Acs Catalysis. 13: 3668-3675. PMID 37124721 DOI: 10.1021/acscatal.3c00107  0.806
2023 Ripak A, De Kreijger S, Sampaio RN, Vincent CA, Cauët É, Jabin I, Tambar UK, Elias B, Troian-Gautier L. Photosensitized Activation of Diazonium Derivatives for C-B Bond Formation. Chem Catalysis. 3. PMID 36936750 DOI: 10.1016/j.checat.2022.100490  0.781
2022 Yetra SR, Schmitt N, Tambar UK. Catalytic photochemical enantioselective α-alkylation with pyridinium salts. Chemical Science. 14: 586-592. PMID 36741522 DOI: 10.1039/d2sc05654b  0.729
2022 Rodriguez M, Kannangara A, Chlebowicz J, Akella R, He H, Tambar UK, Goldsmith EJ. Synthesis and Structural Characterization of Novel Trihalo-sulfone Inhibitors of WNK1. Acs Medicinal Chemistry Letters. 13: 1678-1684. PMID 36262391 DOI: 10.1021/acsmedchemlett.2c00216  0.715
2022 Nair VN, Tambar UK. Catalytic rearrangements of onium ylides in aromatic systems. Organic & Biomolecular Chemistry. 20: 3427-3439. PMID 35388871 DOI: 10.1039/d2ob00218c  0.376
2021 Gartman JA, Tambar UK. Synthetic Studies of the Rubellin Natural Products: Development of a Stereoselective Strategy and Total Synthesis of (+)-Rubellin C. The Journal of Organic Chemistry. PMID 34288689 DOI: 10.1021/acs.joc.1c00920  0.303
2021 Nair VN, Kojasoy V, Laconsay CJ, Kong WY, Tantillo DJ, Tambar UK. Catalyst-Controlled Regiodivergence in Rearrangements of Indole-Based Onium Ylides. Journal of the American Chemical Society. PMID 34124896 DOI: 10.1021/jacs.1c00283  0.367
2020 Sharique M, Tambar UK. N-Heterocyclic carbene based catalytic platform for Hauser-Kraus annulations. Chemical Science. 11: 7239-7243. PMID 34123009 DOI: 10.1039/d0sc03116j  0.309
2020 Gartman JA, Tambar UK. Total Synthesis of (+)-Rubellin C. Organic Letters. PMID 32806220 DOI: 10.1021/Acs.Orglett.0C02127  0.403
2020 Xu B, Troian-Gautier L, Dykstra R, Martin R, Gutierrez O, Tambar UK. Photocatalyzed Diastereoselective Isomerization of Cinnamyl Chlorides to Cyclopropanes. Journal of the American Chemical Society. PMID 32129997 DOI: 10.1021/Jacs.0C00147  0.502
2020 Sharique M, Tambar UK. N-Heterocyclic carbene based catalytic platform for Hauser–Kraus annulations Chemical Science. 11: 7239-7243. DOI: 10.1039/D0Sc03116J  0.422
2019 Xu B, Tambar UK. Remote Allylation of Unactivated C(sp)-H Bonds Triggered by Photogenerated Amidyl Radicals. Acs Catalysis. 9: 4627-4631. PMID 34109055 DOI: 10.1021/acscatal.9b00563  0.32
2019 Qin L, Sharique M, Tambar UK. Controllable, Sequential, and Stereoselective C-H Allylic Alkylation of Alkenes. Journal of the American Chemical Society. PMID 31613609 DOI: 10.1021/Jacs.9B08801  0.445
2019 Xu B, Tambar UK. Remote Allylation of Unactivated C(sp3)–H Bonds Triggered by Photogenerated Amidyl Radicals Acs Catalysis. 9: 4627-4631. DOI: 10.1021/Acscatal.9B00563  0.446
2018 Nash A, Qi X, Maity P, Owens K, Tambar UK. Development of the Vinylogous Pictet-Spengler Cyclization and Total Synthesis of (±)-Lundurine A. Angewandte Chemie (International Ed. in English). PMID 29663602 DOI: 10.1002/Anie.201803702  0.791
2018 Kim D, Nash A, Brabander JD, Tambar UK. Total synthesis of sparstolonin B via a palladium-catalyzed aldehyde α-arylation Tetrahedron. 74: 3787-3790. DOI: 10.1016/J.Tet.2018.05.012  0.48
2017 Bayeh L, Tambar UK. Catalytic Asymmetric Intermolecular Allylic Functionalization of Unactivated Internal Alkenes. Acs Catalysis. 7: 8533-8543. PMID 30009088 DOI: 10.1021/Acscatal.7B03081  0.5
2017 Xu B, Gartman J, Tambar UK. Copper-catalyzed [1,2]-rearrangements of allylic iodides and aryl α-diazoacetates. Tetrahedron. 73: 4150-4159. PMID 28966401 DOI: 10.1016/J.Tet.2017.01.048  0.461
2017 Bayeh L, Le PQ, Tambar UK. Catalytic allylic oxidation of internal alkenes to a multifunctional chiral building block. Nature. PMID 28636605 DOI: 10.1038/Nature22805  0.472
2017 Xu B, Tambar UK. Copper-Catalyzed Enantioselective, Diastereoselective, and Regioselective [2,3]-Rearrangements of Iodonium Ylides. Angewandte Chemie (International Ed. in English). PMID 28600841 DOI: 10.1002/Ange.201705317  0.481
2017 Sleet CE, Tambar UK. Copper-Catalyzed Aminothiolation of 1,3-Dienes via a Dihydrothiazine Intermediate. Angewandte Chemie (International Ed. in English). PMID 28407352 DOI: 10.1002/Anie.201701796  0.49
2017 Tambar UK. New advances in pericyclic reactions Tetrahedron. 73: 4009. DOI: 10.1016/J.Tet.2017.06.014  0.385
2017 Sleet CE, Tambar UK, Maity P. Brønsted acid catalyzed enantioselective pericyclic reactions Tetrahedron. 73: 4023-4038. DOI: 10.1016/J.Tet.2017.02.059  0.669
2016 Xu B, Tambar UK. Ligand-Controlled Regiodivergence in the Copper-Catalyzed [2,3]- and [1,2]-Rearrangements of Iodonium Ylides. Journal of the American Chemical Society. PMID 27603216 DOI: 10.1021/Jacs.6B08624  0.44
2015 Yu Y, Tambar UK. Palladium-Catalyzed Cross-Coupling of α-Bromocarbonyls and Allylic Alcohols for the Synthesis of α-Aryl Dicarbonyl Compounds. Chemical Science (Royal Society of Chemistry : 2010). 6: 2777-2781. PMID 26229586 DOI: 10.1039/C5Sc00505A  0.464
2015 Scheuermann TH, Stroud D, Sleet CE, Bayeh L, Shokri C, Wang H, Caldwell CG, Longgood J, MacMillan JB, Bruick RK, Gardner KH, Tambar UK. Isoform-Selective and Stereoselective Inhibition of Hypoxia Inducible Factor-2. Journal of Medicinal Chemistry. PMID 26226049 DOI: 10.1021/Acs.Jmedchem.5B00529  0.488
2014 Bao H, Bayeh L, Tambar UK. Regioselective and Diastereoselective Aminoarylation of 1,3-Dienes. Chemical Science (Royal Society of Chemistry : 2010). 5: 4863-4867. PMID 25431651 DOI: 10.1039/C4Sc01152J  0.625
2014 Tso SC, Gui WJ, Wu CY, Chuang JL, Qi X, Skvora KJ, Dork K, Wallace AL, Morlock LK, Lee BH, Hutson SM, Strom SC, Williams NS, Tambar UK, Wynn RM, et al. Benzothiophene carboxylate derivatives as novel allosteric inhibitors of branched-chain α-ketoacid dehydrogenase kinase. The Journal of Biological Chemistry. 289: 20583-93. PMID 24895126 DOI: 10.1074/Jbc.M114.569251  0.655
2014 Bao H, Bayeh L, Tambar UK. Allylic functionalization of unactivated olefins with Grignard reagents. Angewandte Chemie (International Ed. in English). 53: 1664-8. PMID 24458538 DOI: 10.1002/Anie.201309134  0.62
2014 Tso SC, Qi X, Gui WJ, Wu CY, Chuang JL, Wernstedt-Asterholm I, Morlock LK, Owens KR, Scherer PE, Williams NS, Tambar UK, Wynn RM, Chuang DT. Structure-guided development of specific pyruvate dehydrogenase kinase inhibitors targeting the ATP-binding pocket. The Journal of Biological Chemistry. 289: 4432-43. PMID 24356970 DOI: 10.1074/Jbc.M113.533885  0.72
2014 Soheili A, Johnson C, Tambar UK. Synthesis of (±)-amathaspiramide F: Stereochemical switch of a [2,3]-stevens rearrangement Strategies and Tactics in Organic Synthesis. 10: 131-154. DOI: 10.1016/B978-0-12-417185-5.00006-5  0.797
2013 Bao H, Bayeh L, Tambar UK. Catalytic Enantioselective Allylic Amination of Olefins for the Synthesis of ent-Sitagliptin. Synlett : Accounts and Rapid Communications in Synthetic Organic Chemistry. 24: 2459-2463. PMID 25378809 DOI: 10.1055/S-0033-1340079  0.655
2013 Maity P, Pemberton RP, Tantillo DJ, Tambar UK. Brønsted acid catalyzed enantioselective indole aza-Claisen rearrangement mediated by an arene CH-O interaction. Journal of the American Chemical Society. 135: 16380-3. PMID 24164401 DOI: 10.1021/Ja4095473  0.666
2013 Soheili A, Tambar UK. Synthesis of (±)-amathaspiramide F and discovery of an unusual stereocontrolling element for the [2,3]-Stevens rearrangement. Organic Letters. 15: 5138-41. PMID 24066807 DOI: 10.1021/Ol4025937  0.793
2013 Nash A, Soheili A, Tambar UK. Stereoselective synthesis of functionalized cyclic amino acid derivatives via a [2,3]-Stevens rearrangement and ring-closing metathesis. Organic Letters. 15: 4770-3. PMID 24001141 DOI: 10.1021/Ol402129H  0.8
2013 Tso SC, Qi X, Gui WJ, Chuang JL, Morlock LK, Wallace AL, Ahmed K, Laxman S, Campeau PM, Lee BH, Hutson SM, Tu BP, Williams NS, Tambar UK, Wynn RM, et al. Structure-based design and mechanisms of allosteric inhibitors for mitochondrial branched-chain α-ketoacid dehydrogenase kinase. Proceedings of the National Academy of Sciences of the United States of America. 110: 9728-33. PMID 23716694 DOI: 10.1073/Pnas.1303220110  0.642
2012 Bao H, Tambar UK. Catalytic enantioselective allylic amination of unactivated terminal olefins via an ene reaction/[2,3]-rearrangement. Journal of the American Chemical Society. 134: 18495-8. PMID 23106555 DOI: 10.1021/Ja307851B  0.672
2011 Soheili A, Tambar UK. Tandem catalytic allylic amination and [2,3]-Stevens rearrangement of tertiary amines. Journal of the American Chemical Society. 133: 12956-9. PMID 21793509 DOI: 10.1021/Ja204717B  0.822
2011 Qi X, Bao H, Tambar UK. Total synthesis of (±)-trigonoliimine C via oxidative rearrangement of an unsymmetrical bis-tryptamine. Journal of the American Chemical Society. 133: 10050-3. PMID 21671591 DOI: 10.1021/Ja203960B  0.743
2011 Bao H, Qi X, Tambar UK. Catalytic enantioselective [2,3]-rearrangements of amine N-oxides. Journal of the American Chemical Society. 133: 1206-8. PMID 21218772 DOI: 10.1021/Ja110500M  0.776
2011 Bao H, Qi X, Tambar UK. Stereoselective [2,3]-rearrangements of amine N -oxides Synlett. 1789-1792. DOI: 10.1055/S-0030-1260962  0.748
2010 Tambar UK, Lee SK, Leighton JL. Enantioselective (formal) aza-Diels-Alder reactions with non-Danishefsky-type dienes. Journal of the American Chemical Society. 132: 10248-50. PMID 20662502 DOI: 10.1021/Ja104480G  0.803
2010 Lee SK, Tambar UK, Perl NR, Leighton JL. Highly enantioselective formal aza-Diels-Alder reactions with acylhydrazones and Danishefsky's diene promoted by a silicon Lewis acid Tetrahedron. 66: 4769-4774. DOI: 10.1016/J.Tet.2010.03.036  0.802
2009 Ebner DC, Tambar UK, Stoltz BM, Storgaard M, Ide ND, Ragan JA, Ellman JA. The direct acyl-alkylation of arynes. Preparation of methyl 2-(2-Acetylphenyl)acetate Organic Syntheses. 86: 161-171.  0.754
2008 Krishnan S, Bagdanoff JT, Ebner DC, Ramtohul YK, Tambar UK, Stoltz BM. Pd-catalyzed enantioselective aerobic oxidation of secondary alcohols: applications to the total synthesis of alkaloids. Journal of the American Chemical Society. 130: 13745-54. PMID 18798630 DOI: 10.1021/Ja804738B  0.769
2007 Tambar UK, Kano T, Zepernick JF, Stoltz BM. The development and scope of a versatile tandem Stille-oxa-electrocyclization reaction Tetrahedron Letters. 48: 345-350. DOI: 10.1016/J.Tetlet.2006.11.097  0.699
2006 Tambar UK, Kano T, Zepernick JF, Stoltz BM. Convergent and diastereoselective synthesis of the polycyclic pyran core of saudin. The Journal of Organic Chemistry. 71: 8357-64. PMID 17064005 DOI: 10.1021/Jo061236+  0.684
2006 Tambar UK, Ebner DC, Stoltz BM. A convergent and enantioselective synthesis of (+)-amurensinine via selective C-H and C-C bond insertion reactions. Journal of the American Chemical Society. 128: 11752-3. PMID 16953603 DOI: 10.1021/Ja0651815  0.785
2005 Tambar UK, Kano T, Stoltz BM. Progress toward the total synthesis of saudin: development of a tandem Stille-oxa-electrocyclization reaction. Organic Letters. 7: 2413-6. PMID 15932211 DOI: 10.1021/Ol050705B  0.701
2005 Tambar UK, Stoltz BM. The direct acyl-alkylation of arynes. Journal of the American Chemical Society. 127: 5340-1. PMID 15826170 DOI: 10.1021/JA050859M  0.553
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