K. Burgess

M. van der Auweraer, K. Burgess, N. Boens, 2009, Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology.

Naturally Assembled Excimers in Xanthenes as Singular and Highly Efficient Laser Dyes in Liquid and Solid Media

K. Burgess, Á. Costela, I. García‐Moreno, 2013 .

Click-Addressable Cassette for Photoaffinity Labeling.

K. Burgess, Bosheng Zhao, 2018, ACS medicinal chemistry letters.

In Vitro and In Vivo Photocytotoxicity of Boron Dipyrromethene Derivatives for Photodynamic Therapy

H. Bergh, G. Wagnières, K. Burgess, 2011 .

An agent for optical imaging of TrkC-expressing, breast cancer.

K. Burgess, Anyanee Kamkaew, Feng Li, 2017, MedChemComm.

Molecular basis of neurotrophin-receptor interactions.

K. Burgess, M. Pattarawarapan, 2003, Journal of medicinal chemistry.

A method for removal of N-BOC protecting groups from substrates on TFA-sensitive resins

K. Burgess, D. Russell, Jieping Zhu, 1998 .

Syntheses of second generation, 14-membered ring β-turn mimics

K. Burgess, Hong-Boon Lee, M. Pattarawarapan, 2003 .

Hows and Whys of Tumor-Seeking Dyes.

K. Burgess, S. Usama, 2021, Accounts of chemical research.

B,O-chelated azadipyrromethenes as near-IR probes.

Michael J. Hall, K. Burgess, R. Bandichhor, 2008, Organic letters.

Base dependence in copper-catalyzed Huisgen reactions: efficient formation of bistriazoles.

K. Burgess, Yu Angell, 2007, Angewandte Chemie.

Chiral N-heterocyclic carbene-transition metal complexes in asymmetric catalysis

K. Burgess, M. Perry, 2003 .

Optically active iridium imidazol-2-ylidene-oxazoline complexes: preparation and use in asymmetric hydrogenation of arylalkenes.

M. T. Powell, K. Burgess, J. Reibenspies, 2003, Journal of the American Chemical Society.

Syntheses of highly fluorescent GFP-chromophore analogues.

K. Burgess, Liangxing Wu, 2008, Journal of the American Chemical Society.

BODIPY dyes in photodynamic therapy.

K. Burgess, L. Kiew, Hong-Boon Lee, 2013, Chemical Society reviews.

BODIPY dyes in photodynamic therapy.

K. Burgess, L. Kiew, Hong-Boon Lee, 2013, Chemical Society reviews.

A Chemoselective Route to β-Enamino Esters and Thioesters

K. Burgess, Dongyue Xin, 2014, Organic letters.

Anthracene-BODIPY cassettes: syntheses and energy transfer.

R. Hochstrasser, K. Burgess, M. Wolford, 2003, Chemistry.

Synthetic helical peptide capping strategies.

K. Burgess, J. Whisenant, 2022, Chemical Society reviews.

Benzophenoxazine-Based Fluorescent Dyes for Labeling Biomolecules

Kevin Burgess, K. Burgess, Jiney Jose, 2006 .

Tetrahedron report number 775 Benzophenoxazine-based fluorescent dyes for labeling biomolecules

K. Burgess, Jiney Jose, 2006 .

Small molecule and protein-based neurotrophic ligands: agonists and antagonists as therapeutic agents

K. Burgess, H. Saragovi, 1999 .

PROTACs suppression of CDK4/6, crucial kinases for cell cycle regulation in cancer.

K. Burgess, Bosheng Zhao, 2019, Chemical communications.

Encapsulated energy-transfer cassettes with extremely well resolved fluorescent outputs.

P. Anzenbacher, K. Burgess, A. Loudet, 2011, Journal of the American Chemical Society.

Blocking Coronavirus 19 Infection via the SARS-CoV-2 Spike Protein: Initial Steps

K. Burgess, J. Whisenant, 2020, ACS medicinal chemistry letters.

Dimeric β-turn peptidomimetics as ligands for the neurotrophin receptor TrkC

K. Burgess, D. Linthicum, K. Gokulan, 2001 .

Fluorescent PARP Inhibitors Applied To Intracranial Glioblastoma: Accumulation and Persistence In Vivo.

K. Burgess, Zhen Yang, Zheng Li, 2022, ACS medicinal chemistry letters.

A designed peptidomimetic agonistic ligand of TrkA nerve growth factor receptors.

A. Cuello, K. Burgess, H. Saragovi, 2000, Molecular pharmacology.

Syntheses of nucleoside triphosphates.

K. Burgess, D. Cook, 2000, Chemical reviews.

MALDI AND FAB MASS SPECTROMETRY OF NUCLEOSIDE TRIPHOSPHATES: A COMPARATIVE STUDY

K. Burgess, D. Russell, A. Shitangkoon, 1996 .

Oligoethylene glycol-substituted aza-BODIPY dyes as red emitting ER-probes.

K. Burgess, Dongyue Xin, N. Wanichacheva, 2015, Organic & biomolecular chemistry.

Bivalent diketopiperazine-based tropomysin receptor kinase C (TrkC) antagonists.

Jing Liu, K. Burgess, H. Saragovi, 2010, Journal of medicinal chemistry.

A peptidomimetic of NT-3 acts as a TrkC antagonist

K. Burgess, Hong-Boon Lee, M. Pattarawarapan, 2009, Peptides.

Bivalent peptidomimetic ligands of TrkC are biased agonists and selectively induce neuritogenesis or potentiate neurotrophin-3 trophic signals.

Yu-Chin Li, K. Burgess, H. Saragovi, 2009, ACS chemical biology.

A monovalent agonist of TrkA tyrosine kinase receptors can be converted into a bivalent antagonist.

E. Purisima, Jing Liu, K. Burgess, 2010, Biochimica et biophysica acta.

TrkC-Targeted Kinase Inhibitors And PROTACs.

K. Burgess, Bosheng Zhao, 2019, Molecular pharmaceutics.

Catalytic homogeneous asymmetric hydrogenations of largely unfunctionalized alkenes.

K. Burgess, Xiuhua Cui, 2005, Chemical reviews.

Conformations of cis- and trans-2,3-methanomethionine stereoisomers in the tripeptide mimic system Ac[cyclo-M]NHiPr.

K. Burgess, C. Ke, 2009, The journal of peptide research : official journal of the American Peptide Society.

Rapid and visual detection of Cd2+ based on aza-BODIPY near infrared dye and its application in real and biological samples for environmental contamination screening.

K. Burgess, Jitnapa Sirirak, N. Wanichacheva, 2020, Journal of hazardous materials.

A Near-Infrared Fluorescence Chemosensor Based on Isothiocyanate-Aza-BODIPY for Cyanide Detection at the Parts per Billion Level: Applications in Buffer Media and Living Cell Imaging.

K. Burgess, Anyanee Kamkaew, V. Promarak, 2019, ChemPlusChem.

K. Burgess, Tianxiong Mi, 2020, ACS medicinal chemistry letters.

Aza-BODIPY dyes with enhanced hydrophilicity.

K. Burgess, A. Kamkaew, 2015, Chemical communications.

Syntheses of regioisomerically pure 5- or 6-halogenated fluoresceins.

K. Burgess, G. Jiao, J. Han, 2003, The Journal of organic chemistry.

The importance of phosphine-to-rhodium ratios in enantioselective hydroborations

K. Burgess, W. Donk, 1994 .

Rigid, conjugated, fluoresceinated thymidine triphosphates: syntheses and polymerase mediated incorporation into DNA analogues.

M. Metzker, K. Burgess, Wade C. Haaland, 2003, Chemistry.

Asymmetric synthesis of 3-phenyl-2,3-methanophenylalanine developed by panning catalysts in a library format

K. Burgess, J. Reibenspies, Mike B. Welch, 1998 .

An allylic/acyclic adenosine nucleoside triphosphate for termination of DNA synthesis by DNA template-dependent polymerases.

R. Gibbs, K. Burgess, L. Thoresen, 1999, Nucleic acids research.

Acyclic nucleoside triphosphate analogs as terminators in biocatalytic DNA replication

R. Gibbs, K. Burgess, C. I. Martinez, 1997 .

Energy transfer cassettes in silica nanoparticles target intracellular organelles.

D. Son, K. Burgess, R. Burghardt, 2011, Organic & biomolecular chemistry.

Flavylium- and Silylrhodapolymethines In Excitation Multiplexing.

K. Burgess, Conghe Tian, 2021, ChemPhotoChem.

A combinatorial method for solution-phase synthesis of labeled bivalent beta-turn mimics.

K. Burgess, H. Saragovi, Yu Angell, 2008, Journal of the American Chemical Society.

Preferred Secondary Structures as a Possible Driving Force for Macrocyclization

K. Burgess, M. Pattarawarapan, S. Roy, 2000 .

Protein-protein interface mimicry by an oxazoline piperidine-2,4-dione.

K. Burgess, Xun Li, Dongyue Xin, 2015, Organic letters.

Transition-metal promoted hydroborations of alkenes, emerging methodology for organic transformations

K. Burgess, Ohlmeyer Michael, 1991 .

Synthetic approaches to stereoisomers and analogues of castanospermine

K. Burgess, Ian Herderson, 1992 .

Carbene-metal hydrides can be much less acidic than phosphine-metal hydrides: significance in hydrogenations.

K. Burgess, Yubo Fan, Ye Zhu, 2010, Journal of the American Chemical Society.

A modular approach to trans-chelating, N-heterocyclic carbene ligand complexes

K. Burgess, Xiuhua Cui, M. Perry, 2002 .

Chiral imidazolylidine ligands for asymmetric hydrogenation of aryl alkenes.

M. T. Powell, K. Burgess, D. Hou, 2001, Journal of the American Chemical Society.

New Optically Active N-Heterocyclic Carbene Complexes for Hydrogenation: A Tale with an Atropisomeric Twist

K. Burgess, J. Reibenspies, Vorawit Banphavichit, 2007 .

TITANIUM-MEDIATED ADDITIONS OF BOROHYDRIDE TO ALKENES

K. Burgess, W. Donk, 1994 .

Chemiluminescent energy-transfer cassettes based on fluorescein and nile red.

Erwen Mei, K. Burgess, Junyan Han, 2007, Angewandte Chemie.

A labeled guanidine ligand for studying sweet taste.

K. Burgess, D. Linthicum, N. Cairns, 1998, Bioorganic & Medicinal Chemistry Letters.

Enantioselective hydroborations catalyzed by rhodium(+1) complexes

K. Burgess, W. Donk, Ohlmeyer Michael, 1991 .

Heterogeneous Phase Transfer Catalysis in Solid Phase Syntheses of Anth-Cyclic Tetrapeptides.

K. Burgess, Kwok‐yin Wong, Dongyue Xin, 2016, Journal of Organic Chemistry.

4,4-Difluoro-4-bora-3a,4a-diaza-s-indacene (BODIPY) dyes modified for extended conjugation and restricted bond rotations.

K. Burgess, A. Burghart, A. Derecskei-Kovacs, 2000, The Journal of organic chemistry.

Synthesis and spectroscopic properties of 2-ketopyrrole–BF2 complexes: a new class of fluorescent dye

K. Burgess, J. Reibenspies, A. Burghart, 2000 .

Regioselective and stereoselective nucleophilic addition to electrophilic vinylcyclopropanes

K. Burgess, 1987 .

Conjugate nucleophilic ring opening of activated vinylcyclopropanes facilitated by homogenous palladium catalysis

K. Burgess, 1985 .

Solid-Phase Organic Synthesis

K. Burgess, 1999 .

Fluorescent proton sensors based on energy transfer.

Roxanne M. Jenkins, K. Burgess, Junyan Han, 2011, The Journal of organic chemistry.

Correlations of structure and rates of energy transfer for through-bond energy-transfer cassettes.

R. Hochstrasser, K. Burgess, A. Loudet, 2006, The journal of physical chemistry. A.

Fluorescent, through-bond energy transfer cassettes for labeling multiple biological molecules in one experiment.

K. Burgess, G. Jiao, L. Thoresen, 2003, Journal of the American Chemical Society.

Energy transfer cassettes based on BODIPY® dyes

K. Burgess, L. Johansson, F. Bergström, 2000 .

On formation of thiohydantoins from amino acids under acylation conditions.

K. Burgess, Samuel Reyes, 2006, The Journal of organic chemistry.

Pyrrolinone-pyrrolidine oligomers as universal peptidomimetics.

T. Ioerger, Eunhwa Ko, K. Burgess, 2011, Journal of the American Chemical Society.

Termination of DNA synthesis by novel 3'-modified-deoxyribonucleoside 5'-triphosphates.

R A Gibbs, M. Metzker, R. Gibbs, 1994, Nucleic acids research.

A cheap, catalytic, scalable, and environmentally benign method for alkene epoxidations.

K. Burgess, B. S. Lane, B. Lane, 2001, Journal of the American Chemical Society.

Microwave-assisted syntheses of regioisomerically pure bromorhodamine derivatives.

K. Burgess, G. Jiao, J. C. Castro, 2003, Organic letters.

Pyrrole-based scaffolds for turn mimics.

Eunhwa Ko, K. Burgess, 2011, Organic letters.

Functionalized BF(2) Chelated Azadipyrromethene Dyes.

K. Burgess, R. Bandichhor, A. Loudet, 2008, Tetrahedron.

Chlorotris(triphenylphosphine)‐rhodium(I)

K. Burgess, Young-Jun Park, W. Donk, 2006 .

Stereochemical assignments via cyclic derivatives: a cautionary note

K. Burgess, K. Whitmire, Ohlmeyer Michael, 1990 .

Asymmetric syntheses of optically active .alpha.,.beta.-disubstituted .beta.-amino acids

K. Burgess, L. Liu, B. Pal, 1993 .

An asymmetric synthesis of D-1,6-Diepicastanospermine

K. Burgess, D. Chaplin, 1992 .

Solution- and solid-phase syntheses of substituted guanidinocarboxylic acids.

K. Burgess, M. Pattarawarapan, A. Zhang, 2000, Journal of combinatorial chemistry.

A route to several stereoisomers of castanospermine

K. Burgess, A. Elbein, I. Henderson, 1992 .

A new approach to swainsonine and castanospermine analogues

K. Burgess, I. Henderson, 1990 .

Anthranilic acid-containing cyclic tetrapeptides: at the crossroads of conformational rigidity and synthetic accessibility.

K. Burgess, Dongyue Xin, 2016, Organic & biomolecular chemistry.

Total Syntheses of Vancomycin.

K. Burgess, A. Zhang, 1999, Angewandte Chemie.

Comparison Of Asymmetric Hydrogenations Of Unsaturated- Carboxylic Acids And -Esters.

K. Burgess, Sakunchai Khumsubdee, 2013, ACS catalysis.

Solid-phase syntheses of beta-turn analogues to mimic or disrupt protein-protein interactions.

K. Burgess, 2001, Accounts of chemical research.

Highly Stereoselective Syntheses of All 1,2,3-Me,OH,Me Triads via Asymmetric Hydrogenation Reactions

K. Burgess, Ye Zhu, 2013 .

Enantioselective Hydroborations Catalyzed by Rhodium(+1) Complexes.

K. Burgess, W. Donk, Ohlmeyer Michael, 1991 .

On deuterium-labeling studies for probing rhodium-catalyzed hydroboration reactions

K. Burgess, W. Donk, A. Kook, 1991 .

Enantioselective hydroboration mediated by homochiral rhodium catalysts

K. Burgess, Ohlmeyer Michael, 1988 .

Manipulation of substrate-controlled diastereoselectivities in hydroborations of acyclic allylamine derivatives

K. Burgess, M. Ohlmeyer, 1991 .

Substrate-controlled diastereoselectivities in catalyzed and uncatalyzed hydroborations of acyclic allylic alcohol derivatives: secondary orbital effects involving d.pi.-p.pi. interactions

K. Burgess, M. Ohlmeyer, J. Cassidy, 1991 .

Substrate-controlled diastereoselectivity in catalyzed and uncatalyzed hydroborations of allylic amine derivatives

K. Burgess, Ohlmeyer Michael, 1989 .

Diastereocontrol in rhodium-catalyzed hydroboration of chiral acyclic allylic alcohol derivatives

K. Burgess, M. Ohlmeyer, 1989 .

Stereochemically matched (and mismatched) bisphosphine ligands: DIOP-DIPAMP hybrids

K. Burgess, M. Ohlmeyer, K. Whitmire, 1992 .

Asymmetric hydrogenation routes to deoxypolyketide chirons.

K. Burgess, Yubo Fan, Jianguang Zhou, 2007, Chemistry.

(η4‐1,5‐Cyclooctadiene)(1‐[(4S)‐(2‐(1‐adamantyl)‐4,5‐dihydrooxazolyl)ethyl]‐3‐(2,6‐diisopropylphenyl)imidazolin‐2‐ylidene)iridium(I) Tetrakis(3,5‐bis(trifluoromethyl)phenyl)borate and (η4‐1,5‐Cyclooctadiene)(1‐[(4R)‐(2‐(1‐adamantyl)‐4,5‐dihydrooxazolyl)ethyl]‐3‐(2,6‐diisopropylphenyl)imidazolin‐2‐yl

K. Burgess, Ye Zhu, 2011 .

Homo-Roche ester derivatives by asymmetric hydrogenation and organocatalysis.

K. Burgess, Hua Zhou, Sakunchai Khumsubdee, 2013, The Journal of organic chemistry.

Asymmetric Syntheses of 2,3-Methanoamino Acids

K. Burgess, K. Ho, D. Moye-Sherman, 1994 .

Comparison of the Effects of (2S,3S)-2,3-Methanomethionine, (2R,3R)-2,3-Methanomethionine, and (2R,3R)-2,3-Methanophenylalanine on the Conformations of Small Peptides

K. Burgess, K. Ho, B. Pal, 1995 .

Synthesis of vicinal dimethyl chirons by asymmetric hydrogenation of trisubstituted alkenes.

K. Burgess, Jian Zhao, 2009, Journal of the American Chemical Society.

Filling gaps in asymmetric hydrogenation methods for acyclic stereocontrol: application to chirons for polyketide-derived natural products.

K. Burgess, Ye Zhu, 2012, Accounts of chemical research.

Reactions of triosmium clusters with organic compounds

K. Burgess, 1984 .

Asymmetric syntheses of all four stereoisomers of 2,3-methanomethionine

K. Burgess, K. Ho, 1992 .

Conformational Preferences of RNase A C-Peptide Derivatives Containing a Highly Constrained Analogue of Phenylalanine

K. Burgess, A. Scholtz, D. Lim, 1998 .

LARGE SCALE SYNTHESES OF N-PROTECTED 2,3-METHANOMETHIONINE STEREOISOMERS

K. Burgess, C. Ke, 1996 .

Synthesis of a valuable cyclopropyl chiron for preparations of 2,3-methanoamino acids

K. Burgess, K. Ho, C. Ke, 1993 .

Asymmetric syntheses of protected derivatives of ornithine- and arginine-2,3-methanologs

K. Burgess, K. Ho, 1992 .

Microwave-assisted functionalization of bromo-fluorescein and bromorhodamine derivatives

K. Burgess, J. C. Castro, J. Han, 2003 .

New and Efficient Synthesis of an Amino Acid for Preparing Phosphine-Functionalized Peptidomimetics

K. Burgess, A. Porte, and Wilfred A. van der Donk, 1998 .

A Reagent for Determining Optical Purities of Diols by Formation of Diastereomeric Arylboronate Esters

K. Burgess, A. Porte, 1994 .

Optically active C 3 -symmetric triarylphosphines in asymmetric allylations

M. T. Powell, K. Burgess, J. Reibenspies, 2001 .

On the efficacy of propeller-shaped, C3-symmetric triarylphosphines in asymmetric catalysis

M. T. Powell, K. Burgess, A. Porte, 1998 .

Enantioselective hydrogenations of arylalkenes mediated by [Ir(cod) (JM-Phos) ]+ complexes.

K. Burgess, J. Reibenspies, T. Colacot, 2001, Chemistry.

Iridium‐Catalyzed Asymmetric Hydrogenation of Vinyl Ethers

K. Burgess, Ye Zhu, 2008 .

Hydroboration reactions mediated by bis(mesityl)niobium: Beware of the trojan horse

K. Burgess, M. Jaspars, 1993 .

Enantioselective esterifications of unsaturated alcohols mediated by a lipase prepared from Pseudomonas sp

K. Burgess, L. Jennings, 1991 .

Stereoselective syntheses of γ-hydroxy-α,β-unsaturated esters: An asymmetric version of the “spac” reaction

K. Burgess, I. Henderson, 1989 .

Accelerated Syntheses and Screening of Stereoselective Transition Metal Catalysts

K. Burgess, A. Porte, 1998 .

Electronic effects steer the mechanism of asymmetric hydrogenations of unfunctionalized aryl-substituted alkenes.

K. Burgess, M. Hall, Yubo Fan, 2004, Journal of the American Chemical Society.

Stereoselective hydrogenations of aryl-substituted dienes.

K. Burgess, Xiuhua Cui, J. Ogle, 2005, Chemical communications.

Lipase-mediated resolutions of SPAC reaction products

K. Burgess, I. Henderson, 1990 .

Conjugate nucleophilic ring opening of activated vinylcyclopropanes facilitated by homogenous palladium catalysis

K. Burgess, 1985 .

Iridium catalyzed enantioselective hydrogenation of α-alkoxy and β-alkoxy vinyl ethers

K. Burgess, Ye Zhu, 2012 .

New Catalysts and Conditions for a CH Insertion Reaction Identified by High Throughput Catalyst Screening

Kevin Burgess, K. Burgess, G. Sulikowski, 1996 .

Biocatalytic desymmetrizations of pentitol derivatives

K. Burgess, I. Henderson, 1991 .

Preparation of a deoxynojirimycin analog containing an imidazole ring

K. Burgess, A. Elbein, Yu-Mei Zeng, 1994 .

Kinetic resolutions of chiral unsaturated alcohols that cannot be resolved efficiently via enantioselective epoxidation

K. Burgess, L. Jennings, 1990 .

Universal peptidomimetics.

Eunhwa Ko, Jing Liu, K. Burgess, 2011, Journal of the American Chemical Society.

New, optically active phosphine oxazoline (JM-Phos) ligands: syntheses and applications in allylation reactions.

K. Burgess, J. Reibenspies, D. Hou, 2001, The Journal of organic chemistry.

Syntheses of Nucleoside Triphosphates

K. Burgess, D. Cook, 2000 .

Expanding the scope of oligo-pyrrolinone-pyrrolidines as protein-protein interface mimics.

K. Burgess, L. Pérez, Dongyue Xin, 2013, The Journal of organic chemistry.

Omegatides: constrained analogs of peptide primary sequence.

Eunhwa Ko, K. Burgess, D. Fedoseyenko, 2012, Organic & biomolecular chemistry.

Reactions of catecholborane with Wilkinson's catalyst: implications for transition metal-catalyzed hydroborations of alkenes

K. Burgess, S. Westcott, J. Calabrese, 1992 .

Optically active building blocks from the SPAC reaction: a completely asymmetric synthesis of (4S-cis)-5-(cyclohexylmethyl)-4-hydroxy-2-pyrrolidinone, a statine analog

K. Burgess, I. Henderson, J. Cassidy, 1991 .

An asymmetric hydrogenation route to (-)-spongidepsin.

K. Burgess, A. Loudet, Ye Zhu, 2010, Organic letters.

Alpha,omega-functionalized 2,4-dimethylpentane dyads and 2,4,6-trimethylheptane triads through asymmetric hydrogenation.

K. Burgess, Jianguang Zhou, 2007, Angewandte Chemie.

Chapter 46. Great Expectations for a Total Synthesis of Vancomycin

K. Burgess, C. I. Martinez, Dongyeol Lim and, 2003 .

Rapid and efficient solid phase syntheses of cyclic peptides with endocyclic biaryl ether bonds

K. Burgess, Jieping Zhu, D. Lim, 1997 .

Syntheses of Nucleosides Designed for Combinatorial DNA Sequencing

R. Gibbs, K. Burgess, Mike B. Welch, 1999 .

Ruthenium-catalyzed hydroborations of alkenes

K. Burgess, M. Jaspars, 1993 .

Iridium-mediated asymmetric hydrogenation of 2,3-diphenylbutadiene: a revealing kinetic study.

K. Burgess, Xiuhua Cui, 2003, Journal of the American Chemical Society.

Aldol-type chirons from asymmetric hydrogenations of trisubstituted alkenes.

K. Burgess, Jian Zhao, 2009, Organic letters.

Asymmetric hydrogenation approaches to valuable, acyclic 1,3-hydroxymethyl chirons.

K. Burgess, Ye Zhu, 2008, Journal of the American Chemical Society.

Synthesis of (S,R,R,S,R,S)-4,6,8,10,16,18- hexamethyldocosane from Antitrogus parvulus via diastereoselective hydrogenations.

K. Burgess, Jianguang Zhou, Ye Zhu, 2007, Organic letters.

An Approach to 2,3-Methanoamino Acids with Extended Side Chains: Syntheses of trans-BOC-cyclo-Lys(CBZ)-OH, trans-BOC-cyclo-Glu-OEt, and trans-BOC-cyclo-Arg(CBZ)-OH

K. Burgess, D. Lim, 1997 .

On titanium-promoted hydroborations of alkenes by borohydride and by catecholborane

K. Burgess, W. Donk, 1994 .

A Platinum‐Gold Cluster: Chloro‐1κCl‐Bis(Triethylphosphine‐1κP)Bis(Triphenyl‐ Phosphine)‐2κP, 3κP‐Triangulo‐ Digold‐Platinum(1 +) Trifluoromethanesulfonate

K. Burgess, M. Ohlmeyer, P. Braunstein, 2007 .

Reaction of the unsaturated mixed metal cluster [Os3(µ-H)(CO)10(µ-AuPR3)](R = Ph, Et) with carbon monoxide and the chemistry of the products; the X-ray crystal structure of [Os3(CO)10(µ-AuPEt3)2]

K. Burgess, P. Raithby, Jack Lewis, 1983 .

Metathesis for catalyst design: metacatalysis

K. Burgess, Sakunchai Khumsubdee, 2014 .

Asymmetric hydrogenation routes to deoxypolyketide chirons.

K. Burgess, Yubo Fan, Jianguang Zhou, 2007, Chemistry.

Heterovalent selectivity and the combinatorial advantage.

Kevin Burgess, Samuel J Reyes, K. Burgess, 2006, Chemical Society reviews.

Chiral 1,3-cyclobutane amino acids: Syntheses and extended conformations

K. Burgess, Shiming Li, Joe Rebenspies, 1997 .

Exploring key orientations at protein-protein interfaces with small molecule probes.

Kevin Burgess, Thomas R Ioerger, T. Ioerger, 2013, Journal of the American Chemical Society.

Biocatalytic resolutions of sulfinylalkanoates: a facile route to optically active sulfoxides

K. Burgess, K. Ho, I. Henderson, 1992 .

Non-covalent delivery of proteins into mammalian cells.

K. Burgess, R. Burghardt, J. Pellois, 2008, Organic & biomolecular chemistry.

The infrared vibrational assignment for the µ2-bridging methylene ligand in metal cluster complexes and its comparison with frequencies assigned to CH2 species chemisorbed on metal surfaces

K. Burgess, N. Sheppard, Jack Lewis, 1982 .

Spirocyclic Peptidomimetics Featuring 2,3-Methanoamino Acids

K. Burgess, D. Lim, 1997 .

Solid‐Phase Syntheses of Unnatural Biopolymers Containing Repeating Urea Units

K. Burgess, D. Linthicum, Hunwoo Shin, 1995 .

Synthesis and reactivity of isocyanatogoldtriosmium clusters

K. Burgess, Jack Lewis, B. Johnson, 1983 .

Syntheses of goldtriosmium-isocyanate clusters

K. Burgess, Jack Lewis, B. Johnson, 1983 .

Photochemistry of Os3(CO)12 with AuPPh3Cl: synthesis and structural characterisation of (µ-AuPPh3)(µ-Cl)Os3(CO)10

K. Burgess, N. Leadbeater, P. Raithby, 1998 .

Syntheses of some organogoldtriosmium clusters; X-ray crystal structure of [Os3(CO)8(PPh3){Au(PPh3)}(2-NHC5H4N)]

K. Burgess, P. Raithby, Jack Lewis, 1983 .

Reactions of [Os3(µ-H)2(CO)10] with organic azides: structural characterization of [Os3(µ-H)(CO)10(µ-HN3Ph)] and [Os3(µ-H)2(CO)9(µ3-NPh)]

K. Burgess, P. Raithby, Jack Lewis, 1982 .

Water-soluble through-bond energy transfer cassettes for intracellular imaging.

K. Burgess, R. Bandichhor, A. Petrescu, 2006, Journal of the American Chemical Society.

Productive Manipulation of Cyanine Dye π-Networks.

K. Burgess, S. Usama, Tye Thompson, 2019, Angewandte Chemie.

Solid Phase Syntheses of Oligoureas

K. Burgess, D. Russell, D. Linthicum, 1997 .

Chiral 1,3‐Cyclobutane Amino Acids: Syntheses and Extended Conformations.

K. Burgess, Shiming Li, Joe Rebenspies, 1997 .

JM-PHOS Ligands: Second-Generation Phosphine Oxazolines for Asymmetric Catalysis

K. Burgess, Duen-Ren Hou and, 1999 .

Reactions of [Os3(µ-H)2(CO)10] with diazo-compounds: structural characterization of [Os3(µ-H)(CO)10(µ-NHNCPh2)] and [Os3(µ-H)(CO)10(µ-NHNCPhMe)]

K. Burgess, P. Raithby, Jack Lewis, 1982 .

μ‐Nitrido‐Bis(Triphenylphosphorus) (1+) μ‐Carbonyl‐Decacarbonyl‐μ‐Hydridotriosmate(1‐)

R. L. Gray, K. Burgess, D. Darensbourg, 2007 .

An iterative route to "decorated" ethylene glycol-based linkers.

K. Burgess, Genliang Lu, Sang Q. Lam, 2006, Chemical communications.

Synthesis and reactivity of triosmium clusters containing a 2-substituted pyridine moiety

K. Burgess, Jack Lewis, B. Johnson, 1982 .

Metallation of 2-ethenylpyridine at triosmium clusters: X-ray crystal structures of the open trinuclear clusters [Os3H(CO)9L(NC5H4CHCH)](L = CO or PMe2Ph)

N. Walker, K. Burgess, M. Hursthouse, 1985 .

Reactions of triosmium clusters with organic azides; x-ray crystal structures of [Os3(CO)10(NCMe)(N3COPh)], [Os3(μ-H)(CO)10(HN3Ph)], and [Os3(μ-H)2(CO)9(μ3-NPh)]

K. Burgess, P. Raithby, Jack Lewis, 1982 .

Functionalization of the 4,4-difluoro-4-bora-3a,4a-diaza-s-indacene (BODIPY) core.

K. Burgess, Lingling Li, B. Nguyen, 2008, Bioorganic & medicinal chemistry letters.

Ring Closure to β-Turn Mimics via Copper-Catalyzed Azide/Alkyne Cycloadditions

K. Burgess, Yu Angell, 2005 .

Anionic and Heteronuclear Triosmium Clusters

K. Burgess, R. D. Adams, Ross P. White, 2007 .

Active targeted ligand-aza-bodipy conjugate for near-infrared photodynamic therapy in melanoma.

K. Burgess, J. Wittayakun, Nanyan Fu, 2020, International journal of pharmaceutics.

Near-infrared aza-BODIPY fluorescent probe for selective Cu2+ detection and its potential in living cell imaging.

K. Burgess, A. Charoenpanich, Jitnapa Sirirak, 2017, Dalton transactions.

Enhanced antiopiate activity and enzyme resistance in a peptidomimetic of FMRFamide containing E-2,3-methanomethionine and E-2,3-methanophenylalanine

Jeffrey A. Jones, K. Burgess, J. Lake, 1996, Peptides.

Subcutaneous injection of an analog of neuropeptide FF precipitates morphine abstinence syndrome.

K. Burgess, J. Lake, D. Malin, 1993, Life sciences.

Manganese-catalyzed epoxidations of alkenes in bicarbonate solutions.

V. DeRose, K. Burgess, B. S. Lane, 2002, Journal of the American Chemical Society.

Preparation of Nano-ZrO2 powder via a microwave-assisted hydrothermal method

K. Burgess, Guangxin Wang, K. Tang, 2021 .

Long-Lasting Rescue of Age-Associated Deficits in Cognition and the CNS Cholinergic Phenotype by a Partial Agonist Peptidomimetic Ligand of TrkA

K. Burgess, R. Quirion, P. Clarke, 2004, The Journal of Neuroscience.

Side Reactions In Organic Synthesis: A Guide to Successful Synthesis Design

K. Burgess, 2005 .

(2R,3R)‐(Z)‐Cyclophenylalanine

K. Burgess, K. Ho, 2001 .

Biocatalytic resolutions of .alpha.-methylene-.beta.-hydroxy esters and ketones

K. Burgess, L. Jennings, 1990 .

A new solid-phase linker for Suzuki coupling with concomitant macrocyclization: synthesis of β-turn mimics

Kevin Burgess, K. Burgess, Wen Li, 1999 .

Comparisons of the conformational biases imposed by trans‐2,3‐methanomethionine and α‐methylmethionine

K. Burgess, D. Lim, D. Moye-Sherman, 1997, Biopolymers.

Syntheses and spectral properties of functionalized, water-soluble BODIPY derivatives.

K. Burgess, Junyan Han, Lingling Li, 2008, The Journal of organic chemistry.

Syntheses, photophysical properties, and application of through-bond energy-transfer cassettes for biotechnology.

M. Metzker, R. Hochstrasser, K. Burgess, 2006, Chemistry.

Substrate‐Controlled Diastereoselectivities in Catalyzed and Uncatalyzed Hydroboration of Acyclic Allylic Alcohol Derivatives: Secondary Orbital Effects Involving dπ‐pπ Interactions.

K. Burgess, M. Ohlmeyer, J. Cassidy, 1991 .

A Near-IR Fluorescent Dasatinib Derivative That Localizes in Cancer Cells.

K. Burgess, S. Usama, Bosheng Zhao, 2019, Bioconjugate chemistry.

Enhanced antiopiate activity and enzyme resistance in peptidomimetics of FMRFamide containing (E)-2,3-methanomethionine

K. Burgess, J. Lake, D. Malin, 1993, Peptides.

Through-space 13C–19F coupling can reveal conformations of modified BODIPY dyes†

K. Burgess, A. Derecskei-Kovacs, J. Reibenspies, 1999 .

Oligonucleotides with strongly fluorescent groups pi-conjugated to a nucleobase: syntheses, melting temperatures, and conformation.

K. Burgess, G. Jiao, 2003, Bioorganic & medicinal chemistry letters.

Stereochemically matched sulfinylacetates for double diastereoselection in the spac reaction

K. Burgess, I. Henderson, 1991 .

Practical asymmetric syntheses of all four 2,3-methanoleucine stereoisomers

K. Burgess, W. Li, 1995 .

Rosamines Targeting the Cancer Oxidative Phosphorylation Pathway

K. Burgess, L. Kiew, Hong-Boon Lee, 2014, PloS one.

New cytotoxic rosamine derivatives selectively accumulate in the mitochondria of cancer cells

K. Burgess, Hong-Boon Lee, Liangxing Wu, 2009, Anti-cancer drugs.

Double-targeting using a TrkC ligand conjugated to dipyrrometheneboron difluoride (BODIPY) based photodynamic therapy (PDT) agent.

K. Burgess, A. Kamkaew, 2013, Journal of medicinal chemistry.

On the stability of furanopyrimidin-2-one bases in oligonucleotides.

K. Burgess, G. Jiao, 2004, Chemical communications.

Selective small molecule peptidomimetic ligands of TrkC and TrkA receptors afford discrete or complete neurotrophic activities.

Yoshua Bengio, K. Burgess, Hong-Boon Lee, 2005, Chemistry & biology.

In vivo studies of nanostructure-based photosensitizers for photodynamic cancer therapy.

K. Burgess, L. Kiew, Hong-Boon Lee, 2014, Small.

Conjugation of Dasatinib with MHI‐148 Has a Significant Advantageous Effect in Viability Assays for Glioblastoma Cells

K. Burgess, S. Usama, R. Sitcheran, 2019, ChemMedChem.

Piptide Chemotypes for Perturbation of the Interaction of Urokinase with Its Receptor.

K. Burgess, Chen-Ming Lin, Maritess Arancillo, 2022, Journal of medicinal chemistry.

Small molecules targeting the NEDD8·NAE protein–protein interaction

K. Burgess, Zhe Gao, Chen-Ming Lin, 2020, Chemical science.

Cyanine-Gemcitabine Conjugates as Targeted Theranostic Agents for Glioblastoma Tumor Cells.

K. Burgess, S. Usama, R. Sitcheran, 2019, Journal of medicinal chemistry.

Small Molecule Ligands For Active Targeting Of TrkC-expressing Tumor Cells.

Eunhwa Ko, K. Burgess, A. Kamkaew, 2012, ACS medicinal chemistry letters.

Synthesis and Solution Conformation of Cyclo[RGDRGD]: A Cyclic Peptide with Selectivity for the αVβ3 Receptor

S. Mousa, K. Burgess, D. Lim, 1996 .

Stereocontrol in Catalyzed and Uncatalyzed Hydroborations

K. Burgess, M. Ohlmeyer, 1992 .

3- and 5-Functionalized BODIPYs via the Liebeskind-Srogl reaction.

K. Burgess, Junyan Han, E. Peña‐Cabrera, 2009, Organic & biomolecular chemistry.

Synthesis of 3,5-Diaryl-4,4-difluoro-4-bora-3a,4a-diaza-s-indacene (BODIPY®) Dyes

K. Burgess, Heejin Kim, A. Burghart, 1998 .

Synthesis of 3,5‐Diaryl‐4,4‐difluoro‐4‐bora‐3a,4a‐diaza‐s‐indacene (BODIPY®) Dyes.

K. Burgess, Heejin Kim, A. Burghart, 1999 .

QuatCy: A Heptamethine Cyanine Modification With Improved Characteristics

H. Choi, K. Burgess, Shinsuke Nomura, 2019, Theranostics.

SNAr Cyclizations To Form Cyclic Peptidomimetics of β-Turns

K. Burgess, Yangbo Feng, Zhicheng Wang, 1998 .

Fluorescent amino- and thiopyronin dyes.

K. Burgess, Liangxing Wu, 2008, Organic letters.

DiSSiMiL: Diverse Small Size Mini-Libraries applied to simple and rapid epitope mapping of a monoclonal antibody.

K. Burgess, W. Zheng, H. Saragovi, 2001, The journal of peptide research : official journal of the American Peptide Society.

Intracellular imaging of organelles with new water-soluble benzophenoxazine dyes.

K. Burgess, R. Burghardt, A. Loudet, 2010, Organic & biomolecular chemistry.

Unconventional Secondary Structure Mimics: Ladder‐Rungs

K. Burgess, J. Whisenant, Chen-Ming Lin, 2020, Angewandte Chemie.

Unconventional Secondary Structure Mimics: Ladder-rungs.

K. Burgess, J. Whisenant, Chen-Ming Lin, 2020, Angewandte Chemie.

Nucleophilic Aromatic Substitution—A Possible Key Step in Total Syntheses of Vancomycin

K. Burgess, D. Lim, C. I. Martinez, 1996 .

Fluorescent kinase inhibitors as probes in cancer.

K. Burgess, S. Usama, Bosheng Zhao, 2021, Chemical Society reviews.

Pyridiniums as potential synthetic substitutes for nitrogen mustards

A. Katritzky, K. Burgess, Ranjan C. Patel, 1982 .

Role of Albumin in Accumulation and Persistence of Tumor-Seeking Cyanine Dyes.

H. Choi, K. Burgess, Shinsuke Nomura, 2020, Bioconjugate chemistry.

A Linker Scaffold to Present Dimers of Pharmacophores Prepared by Solid-Phase Syntheses.

K. Burgess, M. Pattarawarapan, 2000, Angewandte Chemie.

Tropomyosin Receptor Kinase C Targeted Delivery of a Peptidomimetic Ligand-Photosensitizer Conjugate Induces Antitumor Immune Responses Following Photodynamic Therapy

K. Burgess, L. Kiew, Hong-Boon Lee, 2016, Scientific Reports.

On the Mechanisms of Uptake of Tumor-Seeking Cyanine Dyes.

K. Burgess, S. Usama, Chen-Ming Lin, 2018, Bioconjugate chemistry.

PROTAC Compatibilities, Degrading Cell‐Surface Receptors, and the Sticky Problem of Finding a Molecular Glue

K. Burgess, Conghe Tian, 2020, ChemMedChem.

QuatCy-I2 and MHI-I2 in Photodynamic Therapy.

H. Choi, K. Burgess, S. Usama, 2022, ACS medicinal chemistry letters.

Protein labelling and albumin binding characteristics of the near-IR Cy7 fluorophore, QuatCy.

K. Burgess, S. Usama, Sopida Thavornpradit, 2019, Organic & biomolecular chemistry.

Correlations between secondary structure- and protein-protein interface-mimicry: the interface mimicry hypothesis.

T. Ioerger, K. Burgess, Chen-Ming Lin, 2019, Organic & biomolecular chemistry.

Syntheses and properties of water-soluble Nile Red derivatives.

K. Burgess, Jiney Jose, 2006, The Journal of organic chemistry.

Energy transfer dyads based on Nile Red.

K. Burgess, Y. Ueno, Jiney Jose, 2009, Tetrahedron letters.

Water-soluble Nile Blue derivatives: syntheses and photophysical properties.

K. Burgess, Y. Ueno, Jiney Jose, 2009, Chemistry.

A zwitterionic near-infrared dye linked TrkC targeting agent for imaging metastatic breast cancer.

K. Burgess, Feng Li, Zheng Li, 2018, MedChemComm.

Resin type can have important effects on solid phase asymmetricalkylation reactions

K. Burgess, D. Lim, 1997 .

Application of novel phosphine oxazoline ligands in asymmetric allylations of 4-acyloxy-2-pentene derivatives

K. Burgess, A. Porte, 1998 .

Evaluation of "norpeptides" as potential inhibitors of HIV-proteases.

K. Burgess, B. Pal, 1994, Bioorganic & medicinal chemistry.

Application of Novel Phosphine Oxazoline Ligands in Asymmetric Allylations of 4‐Acyloxy‐2‐pentene Derivatives.

K. Burgess, A. Porte, 1998 .

Syntheses and Activities of New C10 β-Turn Peptidomimetics

K. Burgess, Hong-Boon Lee, M. Pattarawarapan, 2004 .

Syntheses and activities of new C10 beta-turn peptidomimetics.

K. Burgess, Hong-Boon Lee, M. Pattarawarapan, 2004, The Journal of organic chemistry.

A small library of peptidomimetics to systematically vary and test the effects of X1 constraints

K. Burgess, C. Godbout, K. Payza, 1996 .

A γ-turn structure induced by 2S,3S-2,3-methanomethionine

B. Pettitt, K. Burgess, K. Ho, 1994 .

A comparison between oxazoline-imidazolinylidene, -imidazolylidine, -benzimidazolylidene hydrogenation catalysts.

K. Burgess, Yubo Fan, Sakunchai Khumsubdee, 2013, The Journal of organic chemistry.

Small Molecule Probes That Perturb A Protein-protein Interface In Antithrombin.

K. Burgess, A. Holzenburg, Dongyue Xin, 2014, Chemical science.

A multifaceted secondary structure mimic based on piperidine-piperidinones.

T. Ioerger, K. Burgess, Dongyue Xin, 2014, Angewandte Chemie.

Bicyclic Schellman Loop Mimics (BSMs): Rigid Synthetic C-Caps for Enforcing Peptide Helicity

K. Burgess, Tianxiong Mi, Duyen Nguyen, 2023, ACS central science.

Resin effects in solid phase SNAr and SN2 macrocyclizations

K. Burgess, Yangbo Feng, 2000 .

Chitosan-Coated Poly(lactic-co-glycolic acid)-Diiodinated boron-Dipyrromethene Nanoparticles Improve Tumor Selectivity and Stealth Properties in Photodynamic Cancer Therapy.

K. Burgess, L. Kiew, Hong-Boon Lee, 2016, Journal of biomedical nanotechnology.

Cyclic semipeptoids: peptoid-organic hybrid macrocycles.

K. Burgess, Ernest Nnanabu, 2006, Organic letters.

Targeted Maytansinoid Conjugate Improves Therapeutic Index for Metastatic Breast Cancer Cells.

K. Burgess, Feng Li, Zheng Li, 2018, Bioconjugate chemistry.

4,4‐Difluoro‐1,3,5,7‐tetramethyl‐4‐bora‐3a,4a‐diaza‐s‐indacene

K. Burgess, R. Bandichhor, N. Bhuvanesh, 2006 .

ASYMMETRIC SYNTHESES OF THE STEREOISOMERS OF PROTECTED 2,3-METHANOGLUTAMINE

K. Burgess, D. Lim, 1995 .

Novel Small Molecule Probes for Metastatic Melanoma.

W. Cai, K. Burgess, Nanyan Fu, 2017, ACS medicinal chemistry letters.

Asymmetric Syntheses of the Stereoisomers of Protected 2,3- Methanoglutamine.

K. Burgess, D. Lim, 1996 .

Synthesis of aminobenzoic Acid-based nonpeptide templates: applications in peptidomimetic drug discovery.

K. Burgess, W. Li, Wen Li, 1999, Methods in molecular medicine.

Evaluating minimalist mimics by exploring key orientations on secondary structures (EKOS).

T. Ioerger, Eunhwa Ko, K. Burgess, 2013, Organic & biomolecular chemistry.

Highly efficient and photostable photonic materials from diiodinated BODIPY laser dyes

K. Burgess, Á. Costela, I. García‐Moreno, 2011 .

Combinatorial Assembly of Small Molecules into Bivalent Antagonists of TrkC or TrkA Receptors

Eunhwa Ko, K. Burgess, A. Malakhov, 2014, PloS one.

Fluorinated and iodinated templates for syntheses of β-turn peptidomimetics

K. Burgess, Luyong Jiang, 2002 .

Facile macrocyclizations to beta-turn mimics with diverse structural, physical, and conformational properties.

K. Burgess, C. Park, 2001, Journal of combinatorial chemistry.

Conformations of Peptidomimetics Formed by SNAr Macrocyclizations: 13‐ to 16‐Membered Ring Systems[≠]

K. Burgess, Yangbo Feng, Zhicheng Wang, 1999 .

Solid‐Phase SNAr Macrocyclizations To Give Turn–Extended‐Turn Peptidomimetics

K. Burgess, Yangbo Feng, 1999 .

Small Molecule Inhibitors of the PCSK9·LDLR Interaction.

K. Burgess, Xiaowen Liang, Bosheng Zhao, 2018, Journal of the American Chemical Society.

Oligonucleotides with Strongly Fluorescent Groups π-Conjugated to a Nucleobase: Syntheses, Melting Temperatures, and Conformation.

K. Burgess, G. Jiao, 2003 .

New templates for syntheses of ring-fused, C(10) beta-turn peptidomimetics leading to the first reported small-molecule mimic of neurotrophin-3.

K. Burgess, M. Pattarawarapan, U. Saragovi, 2002, Journal of medicinal chemistry.

Libraries of opiate and anti-opiate peptidomimetics containing 2,3-methanoleucine.

K. Burgess, R. Rothman, D. Linthicum, 1997, Bioorganic & medicinal chemistry.

Encapsulated Energy-Transfer Cassettes with Extremely Well Resolved Fluorescent Outputs

P. Anzenbacher, K. Burgess, A. Loudet, 2010 .

Enantioselective Esterifications of Unsaturated Alcohols Mediated by a Lipase Prepared from Pseudomonas sp.

K. Burgess, L. Jennings, 2010 .

Correlations between secondary structure- and protein-protein interface-mimicry: the interface mimicry hypothesis.

T. Ioerger, K. Burgess, Chen-Ming Lin, 2019, Organic & biomolecular chemistry.

Fluorescent indicators for intracellular pH.

K. Burgess, Junyan Han, 2010, Chemical reviews.

Anthranilic acid-containing cyclic tetrapeptides: at the crossroads of conformational rigidity and synthetic accessibility.

K. Burgess, Dongyue Xin, 2016, Organic & biomolecular chemistry.

An agent for optical imaging of TrkC-expressing, breast cancer.

K. Burgess, Feng Li, Zheng Li, 2017, MedChemComm.

β-Turn peptidomimetics incorporating i + 1–i + 3 residues: solid phase syntheses and conformational properties

K. Burgess, Samuel Reyes, 2005 .

Produktive Modifikationen von Cyaninfarbstoff‐π‐Netzwerken

K. Burgess, S. Usama, Tye Thompson, 2019, Angewandte Chemie.

Synthesis of aminobenzoic Acid-based nonpeptide templates: applications in peptidomimetic drug discovery.

K. Burgess, Wen Li, 1999, Methods in molecular medicine.

Organelle-selective energy transfer: a fluorescent indicator of intracellular environment.

K. Burgess, R. Burghardt, A. Loudet, 2011, Bioorganic & medicinal chemistry letters.

Design and Optimization of New Phosphine Oxazoline Ligands via High-Throughput Catalyst Screening.

K. Burgess, J. Reibenspies, A. Porte, 1999 .