Kendall N Houk


Ontology type: schema:Person     


Person Info

NAME

Kendall N

SURNAME

Houk

Publications in SciGraph latest 50 shown

  • 2022-05-25 Facile access to fused 2D/3D rings via intermolecular cascade dearomative [2 + 2] cycloaddition/rearrangement reactions of quinolines with alkenes in NATURE CATALYSIS
  • 2022-05-11 Discovery and characterization of a terpene biosynthetic pathway featuring a norbornene-forming Diels-Alderase in NATURE COMMUNICATIONS
  • 2022-04-11 Halogen-bond-assisted radical activation of glycosyl donors enables mild and stereoconvergent 1,2-cis-glycosylation in NATURE CHEMISTRY
  • 2022-03-28 Lattice strain suppresses point defect formation in halide perovskites in NANO RESEARCH
  • 2022-01-12 Allylic C(sp3)–H arylation of olefins via ternary catalysis in NATURE SYNTHESIS
  • 2021-12-09 Enzymatic control of endo- and exo-stereoselective Diels–Alder reactions with broad substrate scope in NATURE CATALYSIS
  • 2021-10-18 An enantioselective ambimodal cross-Diels–Alder reaction and applications in synthesis in NATURE CATALYSIS
  • 2021-09-02 Unveiling the full reaction path of the Suzuki–Miyaura cross-coupling in a single-molecule junction in NATURE NANOTECHNOLOGY
  • 2021-09-02 Facile generation of bridged medium-sized polycyclic systems by rhodium-catalysed intramolecular (3+2) dipolar cycloadditions in NATURE COMMUNICATIONS
  • 2021-08-12 Organocatalytic enantioselective dearomatization of thiophenes by 1,10-conjugate addition of indole imine methides in NATURE COMMUNICATIONS
  • 2021-08-05 Conformational dynamics of androgen receptors bound to agonists and antagonists in SCIENTIFIC REPORTS
  • 2021-07-19 Cleaving arene rings for acyclic alkenylnitrile synthesis in NATURE
  • 2021-03-01 Catalytic mechanism and endo-to-exo selectivity reversion of an octalin-forming natural Diels–Alderase in NATURE CATALYSIS
  • 2021-02-15 Dipolar order in an amphidynamic crystalline metal–organic framework through reorienting linkers in NATURE CHEMISTRY
  • 2021-02-01 Efficient Lewis acid catalysis of an abiological reaction in a de novo protein scaffold in NATURE CHEMISTRY
  • 2021-01-22 Phosphorus(III)-assisted regioselective C–H silylation of heteroarenes in NATURE COMMUNICATIONS
  • 2020-12-14 Catalytic enantioselective synthesis of chiral tetraarylmethanes in NATURE CATALYSIS
  • 2020-10-12 Enzyme-free synthesis of natural phospholipids in water in NATURE CHEMISTRY
  • 2020-09-30 An enzymatic Alder-ene reaction in NATURE
  • 2020-08-26 Intercepting fleeting cyclic allenes with asymmetric nickel catalysis in NATURE
  • 2020-05-25 FAD-dependent enzyme-catalysed intermolecular [4+2] cycloaddition in natural product biosynthesis in NATURE CHEMISTRY
  • 2020-03-23 Demystifying the asymmetry-amplifying, autocatalytic behaviour of the Soai reaction through structural, mechanistic and computational studies in NATURE CHEMISTRY
  • 2020-03-02 Differentiation and functionalization of remote C–H bonds in adjacent positions in NATURE CHEMISTRY
  • 2020-02-17 Aminoperoxide adducts expand the catalytic repertoire of flavin monooxygenases in NATURE CHEMICAL BIOLOGY
  • 2020-02-10 Electronic complementarity permits hindered butenolide heterodimerization and discovery of novel cGAS/STING pathway antagonists in NATURE CHEMISTRY
  • 2020-01-27 Enantioselective C–H functionalization of bicyclo[1.1.1]pentanes in NATURE CATALYSIS
  • 2019-09-30 Metal-free directed sp2-C–H borylation in NATURE
  • 2019-09-23 Controllable catalytic difluorocarbene transfer enables access to diversified fluoroalkylated arenes in NATURE CHEMISTRY
  • 2019-09-23 Fungal indole alkaloid biogenesis through evolution of a bifunctional reductase/Diels–Alderase in NATURE CHEMISTRY
  • 2019-07-22 Structural basis for stereoselective dehydration and hydrogen-bonding catalysis by the SAM-dependent pericyclase LepI in NATURE CHEMISTRY
  • 2019-06-03 Rational design, enantioselective synthesis and catalytic applications of axially chiral EBINOLs in NATURE CATALYSIS
  • 2019-03-13 Enzyme-catalysed [6+4] cycloadditions in the biosynthesis of natural products in NATURE
  • 2019-01-09 Diels-Alder reactivities of cycloalkenediones with tetrazine in JOURNAL OF MOLECULAR MODELING
  • 2018-08-06 Design of catalysts for site-selective and enantioselective functionalization of non-activated primary C–H bonds in NATURE CHEMISTRY
  • 2018-07-30 Diels–Alder cycloadditions of strained azacyclic allenes in NATURE CHEMISTRY
  • 2018-07-19 Enzymatic one-step ring contraction for quinolone biosynthesis in NATURE COMMUNICATIONS
  • 2018-06-27 A promiscuous cytochrome P450 aromatic O-demethylase for lignin bioconversion in NATURE COMMUNICATIONS
  • 2018-06-18 Biosynthesis of thiocarboxylic acid-containing natural products in NATURE COMMUNICATIONS
  • 2018-03-12 Structural basis of the Cope rearrangement and cyclization in hapalindole biogenesis in NATURE CHEMICAL BIOLOGY
  • 2017-09-13 SAM-dependent enzyme-catalysed pericyclic reactions in natural product biosynthesis in NATURE
  • 2017-02-17 A potassium tert-butoxide and hydrosilane system for ultra-deep desulfurization of fuels in NATURE ENERGY
  • 2017-01-23 Enzyme-catalyzed cationic epoxide rearrangements in quinolone alkaloid biosynthesis in NATURE CHEMICAL BIOLOGY
  • 2016-11-11 Biocatalytic trifluoromethylation of unprotected phenols in NATURE COMMUNICATIONS
  • 2016-07-25 MIDA boronates are hydrolysed fast and slow by two different mechanisms in NATURE CHEMISTRY
  • 2015-07-22 Conversion of amides to esters by the nickel-catalysed activation of amide C–N bonds in NATURE
  • 2015-06-29 Enzymatic hydroxylation of an unactivated methylene C–H bond guided by molecular dynamics simulations in NATURE CHEMISTRY
  • 2014-11-24 Substrate control in stereoselective lanthionine biosynthesis in NATURE CHEMISTRY
  • 2014-05-18 A carbonate-forming Baeyer-Villiger monooxygenase in NATURE CHEMICAL BIOLOGY
  • 2014-04-13 The role of distant mutations and allosteric regulation on LovD active site dynamics in NATURE CHEMICAL BIOLOGY
  • 2013-07-10 Metal-free oxidation of aromatic carbon–hydrogen bonds through a reverse-rebound mechanism in NATURE
  • Affiliations

  • University of California, Los Angeles (current)
  • National Institute of Standards and Technology
  • University of Insubria
  • Kodak (United States)
  • Peking University
  • AstraZeneca (United Kingdom)
  • Louisiana State University
  • University of Pennsylvania
  • Nanjing University
  • Carnegie Mellon University
  • University of Arizona
  • Autonomous University of Madrid
  • University of Hong Kong
  • Rutgers, The State University of New Jersey
  • University of Miami
  • Hacettepe University
  • University of Copenhagen
  • Babraham Institute
  • University of Illinois Urbana-Champaign
  • Brandeis University
  • Institute of Medicinal Molecular Design
  • Osaka Sangyo University
  • University of Queensland
  • Université Catholique de Louvain
  • Heidelberg University
  • University of Catania
  • California NanoSystems Institute
  • Bunkyo University
  • Xiamen University
  • University of Pavia
  • UNSW Sydney
  • Duke University
  • University of Washington
  • Columbia University
  • Boğaziçi University
  • University of Wisconsin–Madison
  • Saarland University
  • University of Pittsburgh
  • Barnard College
  • The University of Texas at Austin
  • Ludwig-Maximilians-Universität München
  • California Institute of Technology
  • University of North Texas
  • ETH Zurich
  • Massachusetts Institute of Technology
  • Georgia Institute of Technology
  • The Ohio State University
  • University of Cologne
  • Washington University in St. Louis
  • Keio University
  • MSD (United States)
  • University of Birmingham
  • University of Melbourne
  • University of California System
  • University of California, Berkeley
  • Cornell University
  • Tokyo Institute of Technology
  • Osaka University
  • University of St Andrews
  • University of Massachusetts Amherst
  • University of South Florida
  • Uppsala University
  • Scripps Research Institute
  • University of Bordeaux
  • Oregon State University
  • University of Erlangen-Nuremberg
  • University of Louisville
  • University of California, San Diego
  • Eli Lilly (United States)
  • University of California, Irvine
  • King's College London
  • University of the Ryukyus
  • University of Rochester
  • University of Florida
  • University of Basel
  • University of Oklahoma
  • University of Oxford
  • Technical University of Munich
  • University of Duisburg-Essen
  • Northwestern University
  • University of Oregon
  • Brock University
  • TU Darmstadt
  • University of Würzburg
  • Rice University
  • Fred Hutchinson Cancer Research Center
  • Boston College
  • University of Tokyo
  • Ruhr University Bochum
  • Texas A&M University
  • Stockholm University
  • University of California, Santa Cruz
  • Yale University
  • University of Notre Dame
  • JSON-LD is the canonical representation for SciGraph data.

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