from CaltechAUTHORS

• Yu, Hao; Sercel, Zachary P.; et el. (2023) Total Synthesis of Aleutianamine; Journal of the American Chemical Society; Vol. 145; No. 47; 25533-25537; PMCID PMC10690800; 10.1021/jacs.3c10212
• Nishiura, Yuji; Gonzalez, Kevin J.; et el. (2023) Enantioselective 1,3-Dipolar Cycloadditions of α-Methylene Lactams to Construct Spirocycles; Organic Letters; Vol. 25; No. 35; 6469-6473; PMCID PMC10496134; 10.1021/acs.orglett.3c01978
• Zhang, Tianyi; Nishiura, Yuji; et el. (2023) Palladium-Catalyzed Asymmetric Conjugate Addition of Arylboronic Acids to α,β-Unsaturated Lactams: Enantioselective Construction of All-Carbon Quaternary Stereocenters in Saturated Nitrogen-Containing Heterocycles; Organic Letters; Vol. 25; No. 35; 6479-6484; PMCID PMC10496148; 10.1021/acs.orglett.3c02064
• Kim, Alexia N.; Ngamnithiporn, Aurapat; et el. (2023) Recent Advances in the Total Synthesis of the Tetrahydroisoquinoline Alkaloids (2002–2020); Chemical Reviews; Vol. 123; No. 15; 9447-9496; PMCID PMC10416225; 10.1021/acs.chemrev.3c00054
• Barbor, Jay P.; Nair, Vaishnavi N.; et el. (2023) Development of a Nickel-Catalyzed N–N Coupling for the Synthesis of Hydrazides; Journal of the American Chemical Society; Vol. 145; No. 28; 15071-15077; PMCID PMC10360072; 10.1021/jacs.3c04834
• Greßies, Steffen; Süße, Lars; et el. (2023) Tandem Dearomatization/Enantioselective Allylic Alkylation of Pyridines; Journal of the American Chemical Society; Vol. 145; No. 22; 11907-11913; PMCID PMC10251512; 10.1021/jacs.3c02470
• Flesch, Kaylin N.; Cusumano, Alexander Q.; et el. (2023) Divergent Catalysis: Catalytic Asymmetric [4+2] Cycloaddition of Palladium Enolates; Journal of the American Chemical Society; Vol. 145; No. 20; 11301-11310; 10.1021/jacs.3c02104
• Flesch, Kaylin N.; Cusumano, Alexander Q.; et el. (2023) Divergent Catalysis: Catalytic Asymmetric [4+2] Cycloaddition of Palladium Enolates; Journal of the American Chemical Society; Vol. 145; No. 20; 11301-11310; PMCID PMC10388310; 10.1021/jacs.3c02104
• Hafeman, Nicholas J.; Loskot, Steven A.; et el. (2023) Total synthesis of (−)-scabrolide A and (−)-yonarolide; Chemical Science; Vol. 14; No. 18; 4745-4758; PMCID PMC10173254; 10.1039/d3sc00651d
• Murphy, Sara E.; Crounse, John D.; et el. (2023) Accretion product formation in the self-reaction of ethene-derived hydroxy peroxy radicals; Environmental Science: Atmospheres; 10.1039/d3ea00020f
• Rand, Alexander W.; Gonzalez, Kevin J.; et el. (2023) Total Synthesis of Strempeliopidine and Non-Natural Stereoisomers through a Convergent Petasis Borono-Mannich Reaction; Journal of the American Chemical Society; Vol. 145; No. 13; 7278-7287; PMCID PMC10281614; 10.1021/jacs.2c13146
• Gonzalez, Kevin J.; Rand, Alexander W.; et el. (2023) Development of a Non‐Directed Petasis‐Type Reaction by an Aromaticity‐Disrupting Strategy; Angewandte Chemie International Edition; Vol. 62; No. 14; Art. No. e202218921; PMCID PMC10033435; 10.1002/anie.202218921
• Reimann, Christopher E.; Kim, Kelly E.; et el. (2023) What is a cross-coupling? An argument for a universal definition; Tetrahedron; Vol. 130; Art. No. 133176; PMCID PMC9878734; 10.1016/j.tet.2022.133176
• Hafeman, Nicholas J.; Chan, Melinda; et el. (2022) Asymmetric Total Synthesis of Havellockate; Journal of the American Chemical Society; Vol. 144; No. 44; 20232-20236; PMCID PMC9997676; 10.1021/jacs.2c09583
• Hafeman, Nicholas J.; Chan, Melinda; et el. (2022) Asymmetric Total Synthesis of Havellockate; Journal of the American Chemical Society; Vol. 144; No. 44; 20232-20236; PMCID PMC9997676; 10.1021/jacs.2c09583
• Zhang, Tianyi; Cusumano, Alexander Q.; et el. (2022) Investigations of an Unexpected [2+2] Photocycloaddition in the Synthesis of (−)-Scabrolide A from Quantum Mechanics Calculations; Journal of Organic Chemistry; Vol. 87; No. 21; 14115-14124; 10.1021/acs.joc.2c01693
• Goldstein, Elizabeth L.; Takada, Hirokazu; et el. (2022) Synthesis of enantioenriched 2,2-disubstituted pyrrolidines via sequential asymmetric allylic alkylation and ring contraction; Tetrahedron; Vol. 123; Art. No. 132940; 10.1016/j.tet.2022.132940
• Moghadam, Farbod A.; Hicks, Elliot F.; et el. (2022) Ir-Catalyzed Asymmetric Allylic Alkylation of Dialkyl Malonates Enabling the Construction of Enantioenriched All-Carbon Quaternary Centers; Journal of the American Chemical Society; Vol. 144; No. 18; 7983-7987; 10.1021/jacs.2c02960
• Kim, Alexia N.; Ngamnithiporn, Aurapat; et el. (2022) Iridium-catalyzed asymmetric trans-selective hydrogenation of 1,3-disubstituted isoquinolines; Chemical Science; Vol. 13; No. 11; 3227-3232; PMCID PMC8926345; 10.1039/d1sc06729j
• Chimiak, L.; Eiler, J.; et el. (2022) Isotope effects at the origin of life: Fingerprints of the Strecker synthesis; Geochimica et Cosmochimica Acta; Vol. 321; 78-98; 10.1016/j.gca.2022.01.015
• Samkian, Adrian E.; Sercel, Zachary P.; et el. (2022) Some unusual transformations of a highly reactive α-bromocaranone; Tetrahedron Letters; Vol. 89; Art. No. 153496; 10.1016/j.tetlet.2021.153496
• Kim, Kelly E.; Kim, Alexia N.; et el. (2021) Late-Stage Diversification: A Motivating Force in Organic Synthesis; Journal of the American Chemical Society; Vol. 143; No. 41; 16890-16901; PMCID PMC9285880; 10.1021/jacs.1c08920
• Lohrey, Trevor D.; Cusumano, Alexander Q.; et el. (2021) Identifying the Imperative Role of Metal–Olefin Interactions in Catalytic C–O Reductive Elimination from Nickel(II); ACS Catalysis; Vol. 11; No. 16; 10208-10222; PMCID PMC8849544; 10.1021/acscatal.1c02790
• Sercel, Zachary P.; Sun, Alexander W.; et el. (2021) Synthesis of Enantioenriched gem-Disubstituted 4-Imidazolidinones by Palladium-Catalyzed Decarboxylative Asymmetric Allylic Alkylation; Organic Letters; Vol. 23; No. 16; 6348-6351; PMCID PMC8534816; 10.1021/acs.orglett.1c02134
• Reimann, Christopher E.; Ngamnithiporn, Aurapat; et el. (2021) The Enantioselective Synthesis of Eburnamonine, Eucophylline, and 16′-epi-Leucophyllidine; Angewandte Chemie International Edition; Vol. 60; No. 33; 17957-17962; PMCID PMC8338904; 10.1002/anie.202106184
• Cusumano, Alexander Q.; Houk, K. N.; et el. (2021) Synthetic strategy toward ineleganolide: A cautionary tale; Tetrahedron; Vol. 93; Art. No. 132289; PMCID PMC8294177; 10.1016/j.tet.2021.132289
• Yu, Donna D.; Van Citters, Gregg; et el. (2021) Discovery of novel modulators for the PPARα (peroxisome proliferator activated receptor α): Potential therapies for nonalcoholic fatty liver disease; Bioorganic and Medicinal Chemistry; Vol. 41; Art. No. 116193; 10.1016/j.bmc.2021.116193
• Han, Seo-Jung; Cavitt, Marchello A.; et el. (2021) A Synthetic Strategy toward Eight-Membered Cyclic Amines by Cycloetherification and Claisen Rearrangement; Organic Letters; Vol. 23; No. 9; 3300-3303; PMCID PMC8846577; 10.1021/acs.orglett.1c00763
• Süsse, Lars and Stoltz, Brian M. (2021) Enantioselective Formation of Quaternary Centers by Allylic Alkylation with First-Row Transition-Metal Catalysts; Chemical Reviews; Vol. 121; No. 7; 4084-4099; PMCID PMC8846597; 10.1021/acs.chemrev.0c01115
• Zhang, Gang; Li, Shan; et el. (2021) A covalent p97/VCP ATPase inhibitor can overcome resistance to CB-5083 and NMS-873 in colorectal cancer cells; European Journal of Medicinal Chemistry; Vol. 213; Art. No. 113148; PMCID PMC7954469; 10.1016/j.ejmech.2020.113148
• Sardini, Stephen R. and Stoltz, Brian M. (2021) Discussion Addendum for: Preparation of (S)-tert-ButylPyOx and Palladium-Catalyzed Asymmetric Conjugate Addition of Arylboronic Acids; Organic Syntheses; Vol. 98; 117-130; PMCID PMC9558615; 10.15227/orgsyn.098.0117
• Fulton, Tyler J.; Cusumano, Alexander Q.; et el. (2020) Global Diastereoconvergence in the Ireland–Claisen Rearrangement of Isomeric Enolates: Synthesis of Tetrasubstituted α-Amino Acids; Journal of the American Chemical Society; Vol. 142; No. 52; 21938-21947; PMCID PMC8552564; 10.1021/jacs.0c11480
• Kim, Kelly E.; Sakazaki, Yuka; et el. (2020) Synthesis of non-natural cyanthiwigin–gagunin hybrids through late-stage diversification of the cyanthiwigin natural product core; Tetrahedron; Vol. 76; No. 51; Art. No. 130755; 10.1016/j.tet.2019.130755
• Kim, Alexia N. and Stoltz, Brian M. (2020) Recent Advances in Homogeneous Catalysts for the Asymmetric Hydrogenation of Heteroarenes; ACS Catalysis; Vol. 10; No. 23; 13834-13851; PMCID PMC8460131; 10.1021/acscatal.0c03958
• Cusumano, Alexander Q.; Goddard, William A., III; et el. (2020) Transition Metal Catalyzed [π2s + π2s + σ2s + σ2s] Pericyclic Reaction: Woodward–Hoffmann Rules, Aromaticity, and Electron Flow; Journal of the American Chemical Society; Vol. 142; No. 45; 19033-19039; PMCID PMC8549492; 10.1021/jacs.0c09575
• Ngamnithiporn, Aurapat; Iwayama, Toshihiko; et el. (2020) Enantioselective synthesis of highly oxygenated acyclic quaternary center-containing building blocks via palladium-catalyzed decarboxylative allylic alkylation of cyclic siloxyketones; Chemical Science; Vol. 11; No. 40; 11068-11071; PMCID PMC8162308; 10.1039/d0sc04383d
• Fulton, Tyler J.; Chen, Anthony Y.; et el. (2020) Enantioselective Total Synthesis of (–)-Myrifabral A and B; Chemical Science; Vol. 11; No. 39; 10802-10806; PMCID PMC8162428; 10.1039/d0sc01141j
• Kenseth, Christopher M.; Hafeman, Nicholas J.; et el. (2020) Synthesis of Carboxylic Acid and Dimer Ester Surrogates to Constrain the Abundance and Distribution of Molecular Products in α-Pinene and β-Pinene Secondary Organic Aerosol; Environmental Science and Technology; Vol. 54; No. 20; 12829-12839; 10.1021/acs.est.0c01566
• Wolf, William J.; Li, Jiaming; et el. (2020) Efficient Synthesis of Geminal-Dialkyl Dienes for Olefin Metathesis Polymerization; Macromolecules; Vol. 53; No. 18; 7803-7809; PMCID PMC8297823; 10.1021/acs.macromol.0c01606
• Cusumano, Alexander Q.; Stoltz, Brian M.; et el. (2020) Reaction Mechanism, Origins of Enantioselectivity, and Reactivity Trends in Asymmetric Allylic Alkylation: A Comprehensive Quantum Mechanics Investigation of a C(sp³)–C(sp³) Cross-Coupling; Journal of the American Chemical Society; Vol. 142; No. 32; 13917-13933; PMCID PMC7802888; 10.1021/jacs.0c06243
• Inanaga, Kazato; Wollenburg, Marco; et el. (2020) Catalytic enantioselective synthesis of carbocyclic and heterocyclic spiranes via a decarboxylative aldol cyclization; Chemical Science; Vol. 11; No. 28; 7390-7395; PMCID PMC7574022; 10.1039/d0sc02366c
• Duquette, Douglas C.; Cusumano, Alexander Q.; et el. (2020) Probing Trends in Enantioinduction via Substrate Design: Palladium-Catalyzed Decarboxylative Allylic Alkylation of α-Enaminones; Organic Letters; Vol. 22; No. 13; 4966-4969; PMCID PMC7608880; 10.1021/acs.orglett.0c01441
• Lavernhe, Rémi; Alexy, Eric J.; et el. (2020) Palladium-Catalyzed Enantioselective Decarboxylative Allylic Alkylation of Acyclic α-N-Pyrrolyl/Indolyl Ketones; Organic Letters; Vol. 22; No. 11; 4272-4275; PMCID PMC7608871; 10.1021/acs.orglett.0c01303
• Baek, Doohyun; Ryu, Huijeong; et el. (2020) Catalytic enantioselective synthesis of tetrasubstituted chromanones via palladium-catalyzed asymmetric conjugate arylation using chiral pyridine-dihydroisoquinoline ligands; Chemical Science; Vol. 11; No. 18; 4602-4607; PMCID PMC7574023; 10.1039/d0sc00412j
• Hafeman, Nicholas J.; Loskot, Steven A.; et el. (2020) The Total Synthesis of (–)-Scabrolide A; Journal of the American Chemical Society; Vol. 142; No. 19; 8585-8590; 10.1021/jacs.0c02513
• Kim, Alexia N.; Ngamnithiporn, Aurapat; et el. (2020) Iridium-Catalyzed Enantioselective and Diastereoselective Hydrogenation of 1,3-Disubstituted Isoquinolines; ACS Catalysis; Vol. 10; No. 5; 3241-3248; PMCID PMC8152574; 10.1021/acscatal.0c00211
• Jette, Carina I.; Tong, Z. Jaron; et el. (2020) Copper-Catalyzed Enantioselective Allylic Alkylation with a γ-Butyrolactone-Derived Silyl Ketene Acetal; Angewandte Chemie International Edition; Vol. 59; No. 5; 2033-2038; PMCID PMC7051182; 10.1002/anie.201912618
• Lavernhe, Rémi; Alexy, Eric J.; et el. (2020) Palladium-Catalyzed Enantioselective Decarboxylative Allylic Alkylation of Protected Benzoin-Derived Enol Carbonates; Advanced Synthesis and Catalysis; Vol. 362; No. 2; 344-347; PMCID PMC7942817; 10.1002/adsc.201901281
• Park, Dongseong; Jette, Carina I.; et el. (2020) Enantioselective Alkynylation of Trifluoromethyl Ketones Catalyzed by Cation-Binding Salen Nickel Complexes; Angewandte Chemie International Edition; Vol. 59; No. 2; 775-779; 10.1002/anie.201913057
• Li, Jiaming; Stoltz, Brian M.; et el. (2019) Enantioselective Synthesis of 15-Deoxy-Δ¹²,¹⁴-Prostaglandin J₂; Organic Letters; Vol. 21; No. 24; 10139-10142; 10.1021/acs.orglett.9b04198
• Wright, Austin C. and Stoltz, Brian M. (2019) Enantioselective construction of the tricyclic core of curcusones A–D via a cross-electrophile coupling approach; Chemical Science; Vol. 10; No. 45; 10562-10565; PMCID PMC6988747; 10.1039/c9sc04127c
• Wright, Austin C.; Lee, Chung Whan; et el. (2019) Progress toward the Enantioselective Synthesis of Curcusones A–D via a Divinylcyclopropane Rearrangement Strategy; Organic Letters; Vol. 21; No. 23; 9658-9662; 10.1021/acs.orglett.9b03829
• Sercel, Zachary P.; Sun, Alexander W.; et el. (2019) Palladium-Catalyzed Decarboxylative Asymmetric Allylic Alkylation of 1,4-Diazepan-5-ones; Organic Letters; Vol. 21; No. 22; 9158-9161; PMCID PMC8579948; 10.1021/acs.orglett.9b03530
• Velasco-Rubio, Álvaro; Alexy, Eric J.; et el. (2019) Stereospecific Overman Rearrangement of Substituted Cyclic Vinyl Bromides: Access to Fully Substituted α-Amino Ketones; Organic Letters; Vol. 21; No. 22; 8962-8965; 10.1021/acs.orglett.9b03347
• Sun, Alexander W.; Lackner, Sebastian; et el. (2019) Modularity: Adding New Dimensions to Total Synthesis; Trends in Chemistry; Vol. 1; No. 7; 630-643; 10.1016/j.trechm.2019.05.008
• Jones, Christopher G.; Asay, Matthew; et el. (2019) Characterization of Reactive Organometallic Species via MicroED; ACS Central Science; Vol. 5; No. 9; 1507-1513; PMCID PMC6764211; 10.1021/acscentsci.9b00403
• Sun, Alexander W.; Bulterys, Philip L.; et el. (2019) Incorporation of a chiral gem-disubstituted nitrogen heterocycle yields an oxazolidinone antibiotic with reduced mitochondrial toxicity; Bioorganic and Medicinal Chemistry Letters; Vol. 29; No. 18; 2686-2689; PMCID PMC6711789; 10.1016/j.bmcl.2019.07.024
• Wright, Austin C.; Du, Yun Emily; et el. (2019) A Small-scale Procedure for Acid-catalyzed Ketal Formation; Journal of Organic Chemistry; Vol. 84; No. 17; 11258-11260; 10.1021/acs.joc.9b01541
• Fulton, Tyler J.; Wu, Brenda; et el. (2019) Palladium-catalyzed α,β-dehydrogenation of acyclic ester equivalents promoted by a novel electron deficient phosphinooxazoline ligand; Tetrahedron; Vol. 75; No. 31; 4104-4109; PMCID PMC7119178; 10.1016/j.tet.2019.05.065
• Alexy, Eric J.; Fulton, Tyler J.; et el. (2019) Palladium-catalyzed enantioselective decarboxylative allylic alkylation of fully substituted N-acyl indole-derived enol carbonates; Chemical Science; Vol. 10; No. 23; 5996-6000; PMCID PMC6566452; 10.1039/c9sc01726g
• Craig, Robert A., II; Smith, Russell C.; et el. (2019) Unified Enantioselective, Convergent Synthetic Approach Toward the Furanobutenolide-Derived Polycyclic Norcembranoid Diterpenes: Synthesis of a Series of Ineleganoloids by Oxidation State Manipulation of the Carbocyclic Core; Journal of Organic Chemistry; Vol. 84; No. 12; 7722-7746; 10.1021/acs.joc.9b00635
• Harned, Andrew M. and Stoltz, Brian M. (2019) Development of a catalytic enantioselective synthesis of the guanacastepene and heptemerone tricyclic core; Tetrahedron; Vol. 75; No. 24; 3166-3177; PMCID PMC6959853; 10.1016/j.tet.2019.02.053
• Lee, Chung Whan; Taylor, Buck L. H.; et el. (2019) An unexpected Ireland–Claisen rearrangement cascade during the synthesis of the tricyclic core of Curcusone C: Mechanistic elucidation by trial-and-error and automatic artificial force-induced reaction (AFIR) computations; Journal of the American Chemical Society; Vol. 141; No. 17; 6995-7004; 10.1021/jacs.9b01146
• Wright, Austin C. and Stoltz, Brian M. (2019) Discussion Addendum for: The Direct Acyl-Alkylation of Arynes. Preparation of Methyl 2-(2-acetylphenyl)acetate; Organic Syntheses; Vol. 96; 80-97
• Yamano, Michael M.; Knapp, Rachel R.; et el. (2019) Cycloadditions of Oxacyclic Allenes and a Catalytic Asymmetric Entryway to Enantioenriched Cyclic Allenes; Angewandte Chemie International Edition; Vol. 58; No. 17; 5653-5657; PMCID PMC6456397; 10.1002/anie.201900503
• Jette, Carina I.; Geibel, Irina; et el. (2019) Palladium-Catalyzed Construction of Quaternary Stereocenters by Enantioselective Arylation of γ-Lactams with Aryl Chlorides and Bromides; Angewandte Chemie International Edition; Vol. 58; No. 13; 4297-4301; 10.1002/anie.201814475
• Han, Seo-Jung; Bhat, Vikram; et el. (2019) Atroposelective Synthesis of PINAP via Dynamic Kinetic Asymmetric Transformation; Advanced Synthesis and Catalysis; Vol. 361; No. 3; 441-444; 10.1002/adsc.201801248
• Sun, Alexander W.; Hess, Stephan N.; et el. (2019) Enantioselective synthesis of gem-disubstituted N-Boc diazaheterocycles via decarboxylative asymmetric allylic alkylation; Chemical Science; Vol. 10; No. 3; 788-792; PMCID PMC6345351; 10.1039/c8sc03967d
• Welin, Eric R.; Ngamnithiporn, Aurapat; et el. (2019) Concise total syntheses of (–)-jorunnamycin A and (–)-jorumycin enabled by asymmetric catalysis; Science; Vol. 363; No. 6424; 270-275; PMCID PMC7017906; 10.1126/science.aav3421
• Praske, Eric; Otkjær, Rasmus V.; et el. (2019) Intramolecular Hydrogen Shift Chemistry of Hydroperoxy-Substituted Peroxy Radicals; Journal of Physical Chemistry A; Vol. 123; No. 2; 590-600; 10.1021/acs.jpca.8b09745
• Li, Jiaming; Ahmed, Tonia S.; et el. (2019) Concise Syntheses of Δ^(12)-Prostaglandin J Natural Products via Stereoretentive Metathesis; Journal of the American Chemical Society; Vol. 141; No. 1; 154-158; 10.1021/jacs.8b12816
• Shockley, Samantha E.; Hethcox, J. Caleb; et el. (2018) Intermolecular Stereoselective Iridium-Catalyzed Allylic Alkylation: An Evolutionary Account; Synlett; Vol. 29; No. 19; 2481-2492; PMCID PMC6870865; 10.1055/s-0037-1610217
• Jones, Christopher G.; Martynowycz, Michael W.; et el. (2018) The CryoEM Method MicroED as a Powerful Tool for Small Molecule Structure Determination; ACS Central Science; Vol. 4; No. 11; 1587-1592; PMCID PMC6276044; 10.1021/acscentsci.8b00760
• Davies, Huw M. L.; Itami, Kenichiro; et el. (2018) New directions in natural product synthesis; Chemical Society Reviews; Vol. 47; No. 21; 7828-7829; 10.1039/c8cs90115e
• Liu, Wenbin; Ren, Zhi; et el. (2018) Catalyst-Controlled Selective Functionalization of Unactivated C–H Bonds in the Presence of Electronically Activated C–H Bonds; Journal of the American Chemical Society; Vol. 140; No. 38; 12247-12255; 10.1021/jacs.8b07534
• Lu, Yanhui; Goldstein, Elizabeth L.; et el. (2018) Palladium-Catalyzed Enantioselective C_(sp)^3–C_(sp)3 Cross-Coupling for the Synthesis of (Poly)fluorinated Chiral Building Blocks; Organic Letters; Vol. 20; No. 18; 5657-5660; PMCID PMC6192028; 10.1021/acs.orglett.8b02369
• Wang, Xin; Zhu, Ming-Hui; et el. (2018) General and Practical Potassium Methoxide/Disilane-Mediated Dehalogenative Deuteration of (Hetero)Arylhalides; Journal of the American Chemical Society; Vol. 140; No. 35; 10970-10974; 10.1021/jacs.8b07597
• Alexy, Eric J.; Zhang, Haiming; et el. (2018) Catalytic Enantioselective Synthesis of Acyclic Quaternary Centers: Palladium-Catalyzed Decarboxylative Allylic Alkylation of Fully Substituted Acyclic Enol Carbonates; Journal of the American Chemical Society; Vol. 140; No. 32; 10109-10112; PMCID PMC6103296; 10.1021/jacs.8b05560
• Kenseth, Christopher M.; Huang, Yuanlong; et el. (2018) Synergistic O₃ + OH oxidation pathway to extremely low-volatility dimers revealed in β-pinene secondary organic aerosol; Proceedings of the National Academy of Sciences of the United States of America; Vol. 115; No. 33; 8301-8306; PMCID PMC6099901; 10.1073/pnas.1804671115
• Defieber, Christian; Mohr, Justin T.; et el. (2018) Short Enantioselective Formal Synthesis of (–)-Platencin; Synthesis-Stuttgart; Vol. 50; No. 22; 4359-4368; PMCID PMC6498846; 10.1055/s-0037-1610437
• Hartrampf, Nina; Winter, Nils; et el. (2018) Total Synthesis of the Norhasubanan Alkaloid Stephadiamine; Journal of the American Chemical Society; Vol. 140; No. 28; 8675-8680; PMCID PMC6130314; 10.1021/jacs.8b01918
• Hethcox, J. Caleb; Shockley, Samantha E.; et el. (2018) Enantioselective Synthesis of Vicinal All-Carbon Quaternary Centers via Iridium-Catalyzed Allylic Alkylation; Angewandte Chemie International Edition; Vol. 57; No. 28; 8664-8667; PMCID PMC6033654; 10.1002/anie.201804820
• Krout, Michael R.; Henry, Christopher E.; et el. (2018) Wolff/Cope Approach to the AB Ring of the Sesterterpenoid Variecolin; Journal of Organic Chemistry; Vol. 83; No. 13; 6995-7009; PMCID PMC6035096; 10.1021/acs.joc.7b02972
• Pritchett, Beau P. and Stoltz, Brian M. (2018) Enantioselective palladium-catalyzed allylic alkylation reactions in the synthesis of Aspidosperma and structurally related monoterpene indole alkaloids; Natural Product Reports; Vol. 35; No. 6; 559-574; PMCID PMC6013405; 10.1039/c7np00069c
• Craig, Robert A., II; Smith, Russell C.; et el. (2018) Development of a Unified Enantioselective, Convergent Synthetic Approach Toward the Furanobutenolide-Derived Polycyclic Norcembranoid Diterpenes: Asymmetric Formation of the Polycyclic Norditerpenoid Carbocyclic Core by Tandem Annulation Cascade; Journal of Organic Chemistry; Vol. 83; No. 7; 3467-3485; PMCID PMC5889334; 10.1021/acs.joc.7b02825
• Kim, Kelly E.; Adams, Ashley M.; et el. (2018) The Cyanthiwigin Natural Product Core as a Complex Molecular Scaffold for Comparative Late-Stage C–H Functionalization Studies; Journal of Organic Chemistry; Vol. 83; No. 6; 3023-3033; 10.1021/acs.joc.7b03291
• Ngamnithiporn, Aurapat; Jette, Carina I.; et el. (2018) Nickel-catalyzed enantioselective allylic alkylation of lactones and lactams with unactivated allylic alcohols; Chemical Science; Vol. 2018; No. 9; 2547-2551; PMCID PMC5912103; 10.1039/c7sc05216b
• Leung, Joyce C.; Bedermann, Aaron A.; et el. (2018) Total Synthesis of (±)-Phomoidride D; Angewandte Chemie International Edition; Vol. 57; No. 7; 1991-1994; 10.1002/anie.201712369
• Duquette, Douglas Charles; Jensen, Thomas; et el. (2018) Progress towards the total synthesis of hamigerans C and D: a direct approach to an elaborated 6-7-5 carbocyclic core; Journal of Antibiotics; Vol. 71; No. 2; 263-267; PMCID PMC5788718; 10.1038/ja.2017.96
• Chen, Anthony Y.; Lu, Qianqian; et el. (2018) Isocanthine Synthesis via Rh(III)-Catalyzed Intramolecular C-H Functionalization; Journal of Organic Chemistry; Vol. 83; No. 1; 330-337; 10.1021/acs.joc.7b02731
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