https://doyle.chem.ucla.edu/avada_faq/enantioselective-ring-opening-of-epoxides-by-fluoride-anion-promoted-by-a-cooperative-dual-catalyst-system/2020-09-21T17:53:41-07:00https://doyle.chem.ucla.edu/avada_faq/palladium-catalyzed-asymmetric-synthesis-of-allylic-fluorides/2020-09-21T17:53:34-07:00https://doyle.chem.ucla.edu/avada_faq/9-transition-metal-catalyzed-cross-coupling-with-n-acyliminium-ions-derived-from-quinolines-and-isoquinolines/2020-09-21T17:53:29-07:00https://doyle.chem.ucla.edu/avada_faq/10-nickel-catalyzed-cross-coupling-of-styrenyl-epoxides-with-boronic-acids/2020-09-21T17:53:24-07:00https://doyle.chem.ucla.edu/avada_faq/11-mechanistic-investigations-of-cooperative-catalysis-in-the-enantioselective-fluorination-of-epoxides/2020-09-21T17:53:19-07:00https://doyle.chem.ucla.edu/avada_faq/12-palladium-catalyzed-regio-and-enantioselective-fluorination-of-acyclic-allylic-halides/2020-09-21T17:53:13-07:00https://doyle.chem.ucla.edu/avada_faq/13-fluoride-ring-opening-kinetic-resolution-of-terminal-epoxides-preparation-of-s-2-fluoro-1-phenylethanol/2020-09-21T17:53:07-07:00https://doyle.chem.ucla.edu/avada_faq/14-nickel-catalyzed-cross-coupling-of-chromene-acetals-and-boronic-acids/2020-09-21T17:53:02-07:00https://doyle.chem.ucla.edu/avada_faq/15-nickel-catalyzed-negishi-alkylations-of-styrenyl-aziridines/2020-09-21T17:52:59-07:00https://doyle.chem.ucla.edu/avada_faq/16-synthesis-of-%ce%b2-fluoroamines-by-lewis-base-catalyzed-hydrofluorination-of-aziridines/2020-09-21T17:52:34-07:00https://doyle.chem.ucla.edu/avada_faq/17-mechanistic-investigation-of-the-nickel-catalyzed-suzuki-reaction-of-no-acetals-evidence-for-boronic-acid-assisted-oxidative-addition-and-an-iminium-activation-pathway/2020-09-21T17:52:29-07:00https://doyle.chem.ucla.edu/avada_faq/18-carbofluorination-via-a-palladium-catalyzed-cascade-reaction/2022-12-30T15:43:28-08:00https://doyle.chem.ucla.edu/avada_faq/19-enantioselective-fluoride-ring-opening-of-aziridines-enabled-by-cooperative-lewis-acid-catalysis/2022-12-30T15:46:02-08:00https://doyle.chem.ucla.edu/avada_faq/20-nickel-catalyzed-enantioselective-arylation-of-pyridinium-ions-harnessing-an-iminium-ion-activation-mode/2020-09-21T17:52:12-07:00https://doyle.chem.ucla.edu/avada_faq/21-palladium-catalyzed-allylic-c-h-fluorination/2020-09-21T17:52:06-07:00https://doyle.chem.ucla.edu/avada_faq/22-directed-nickel-catalyzed-negishi-cross-coupling-of-alkyl-aziridines/2022-12-30T15:50:05-08:00https://doyle.chem.ucla.edu/avada_faq/23-enantioselective-nickel-catalyzed-suzuki-cross-coupling-of-quinolinium-ions/2020-09-21T17:51:48-07:00https://doyle.chem.ucla.edu/avada_faq/24-mechanistic-investigations-of-palladium-catalyzed-allylic-fluorination/2020-09-21T17:51:43-07:00https://doyle.chem.ucla.edu/avada_faq/25-enantioselective-radiosynthesis-of-positron-emission-tomography-pet-tracers-containing-18ffluorohydrins/2020-09-21T17:51:36-07:00https://doyle.chem.ucla.edu/avada_faq/26-the-chemistry-of-transition-metals-with-three-membered-ring-heterocycles/2020-09-21T17:51:30-07:00https://doyle.chem.ucla.edu/avada_faq/27-merging-photoredox-with-nickel-catalysis-coupling-of-%ce%b1-carboxyl-sp3-carbons-with-aryl-halides/2022-12-30T15:51:05-08:00https://doyle.chem.ucla.edu/avada_faq/28-a-modular-air-stable-nickel-precatalyst/2020-09-21T17:51:23-07:00https://doyle.chem.ucla.edu/avada_faq/29-electron-deficient-olefin-ligands-enable-generation-of-quaternary-carbons-by-ni-catalyzed-cross-coupling/2020-09-21T17:51:21-07:00https://doyle.chem.ucla.edu/avada_faq/30-dialkyl-ether-formation-via-nickel-catalyzed-cross-coupling-of-acetals-and-aryl-iodides/2020-09-21T17:50:44-07:00https://doyle.chem.ucla.edu/avada_faq/31-pyfluor-a-low-cost-stable-and-selective-deoxyfluorination-reagent/2020-09-21T17:50:38-07:00https://doyle.chem.ucla.edu/avada_faq/32-direct-acylation-of-csp3%e2%88%92h-bonds-enabled-by-nickel-and-photoredox-catalysis/2020-09-21T17:50:34-07:00https://doyle.chem.ucla.edu/avada_faq/33-nickel-catalyzed-enantioselective-arylation-of-pyridine/2020-09-21T17:50:28-07:00https://doyle.chem.ucla.edu/avada_faq/34-c-h-functionalization-of-amines-with-aryl-halides-by-nickel-photoredox-catalysis/2022-12-30T15:52:25-08:00https://doyle.chem.ucla.edu/avada_faq/35-nucleophilic-radiofluorination-of-%ce%b1-diazocarbonyl-compounds-enabled-by-copper-catalyzed-h-f-insertion/2020-09-21T17:50:17-07:00https://doyle.chem.ucla.edu/avada_faq/36-direct-csp3%e2%88%92h-cross-coupling-enabled-by-catalytic-generation-of-chlorine-radicals/2020-09-21T17:50:12-07:00https://doyle.chem.ucla.edu/avada_faq/37-parameterization-of-phosphine-ligands-demonstrates-enhancement-of-nickel-catalysis-via-remote-steric-effects/2020-09-21T17:50:08-07:00https://doyle.chem.ucla.edu/avada_faq/38-nickel-photoredox-catalyzed-enantioselective-desymmetrization-of-meso-cyclic-anhydrides/2020-09-21T17:50:03-07:00https://doyle.chem.ucla.edu/avada_faq/39-nickel-catalyzed-enantioselective-reductive-cross-coupling-of-styrenyl-aziridines/2020-09-21T17:50:00-07:00https://doyle.chem.ucla.edu/avada_faq/40-mild-redox-neutral-formylation-of-aryl-chlorides-via-photocatalytic-generation-of-chlorine-radicals/2020-09-21T17:49:28-07:00https://doyle.chem.ucla.edu/avada_faq/41-ni-catalyzed-carbon-carbon-bond-forming-reductive-amination/2020-09-21T17:49:22-07:00https://doyle.chem.ucla.edu/avada_faq/42-long-lived-charge-transfer-states-of-nickelii-aryl-halide-complexes-facilitate-bimolecular-photoinduced-electron-transfer/2022-12-30T15:57:11-08:00https://doyle.chem.ucla.edu/avada_faq/43-predicting-reaction-performance-in-c-n-cross-coupling-using-machine-learning/2022-12-30T16:31:17-08:00https://doyle.chem.ucla.edu/avada_faq/44-deoxyfluorination-with-sulfonyl-fluorides-navigating-reaction-space-with-machine-learning/2022-12-30T16:00:14-08:00https://doyle.chem.ucla.edu/avada_faq/45-direct-c-c-bond-formation-from-alkanes-using-ni-photoredox-catalysis/2022-12-30T16:00:58-08:00https://doyle.chem.ucla.edu/avada_faq/46-generation-of-phosphoranyl-radicals-via-photoredox-catalysis-enables-voltage-independent-activation-of-strong-c-o-bonds/2022-12-30T16:01:28-08:00https://doyle.chem.ucla.edu/avada_faq/47-response-to-comment-on-predicting-reaction-performance-in-c-n-cross-coupling-using-machine-learning/2022-12-30T16:30:25-08:00https://doyle.chem.ucla.edu/avada_faq/48-discrete-object-generation-with-reversible-inductive-construction/2022-12-30T16:07:20-08:00https://doyle.chem.ucla.edu/avada_faq/49-direct-use-of-carboxylic-acids-in-the-photocatalytic-hydroacylation-of-styrenes-to-generate-dialkyl-ketones/2022-12-30T16:11:21-08:00https://doyle.chem.ucla.edu/avada_faq/50-3d-d-excited-states-of-niii-complexes-relevant-to-photoredox-catalysis-spectroscopic-identification-and-mechanistic-implications/2022-12-30T16:12:00-08:00https://doyle.chem.ucla.edu/avada_faq/51-synthesis-of-%ce%b2-phenethylamines-via-ni-photoredox-cross-electrophile-coupling-of-aliphatic-aziridines-and-aryl-iodides/2022-12-30T16:13:22-08:00https://doyle.chem.ucla.edu/avada_faq/52-nickel-photoredox-catalyzed-methylation-of-heteroaryl-chlorides-using-trimethyl-orthoformate-as-a-methyl-radical-source/2022-12-30T16:13:51-08:00https://doyle.chem.ucla.edu/avada_faq/53-role-of-electron-deficient-olefin-ligands-in-a-ni-catalyzed-aziridine-cross-coupling-to-generate-quaternary-carbons/2022-12-30T16:14:27-08:00https://doyle.chem.ucla.edu/avada_faq/54-regioselective-cross-electrophile-coupling-of-epoxides-and-heteroaryl-iodides-via-ni-ti-photoredox-catalysis/2022-12-30T16:17:21-08:00https://doyle.chem.ucla.edu/avada_faq/55-nucleophilic-radiofluorination-of-redox-active-esters-via-radical-polar-crossover-enabled-by-photoredox-catalysis/2022-12-30T16:18:13-08:00https://doyle.chem.ucla.edu/avada_faq/56-bioinspiration-in-light-harvesting-and-catalysis/2022-12-30T20:35:01-08:00https://doyle.chem.ucla.edu/avada_faq/57-synthetic-and-mechanistic-implications-of-chlorine-photoelimination-in-nickel-photoredox-csp3-h-cross-coupling/2022-12-30T20:34:14-08:00https://doyle.chem.ucla.edu/avada_faq/58-bayesian-reaction-optimization-as-a-tool-for-chemical-synthesis/2022-12-30T16:28:13-08:00https://doyle.chem.ucla.edu/avada_faq/59-automation-and-computer-assisted-planning-for-chemical-synthesis/2022-12-30T20:33:39-08:00https://doyle.chem.ucla.edu/avada_faq/60-predicting-reaction-yields-via-supervised-learning/2022-12-30T20:33:10-08:00https://doyle.chem.ucla.edu/avada_faq/61-ni-photoredox-catalyzed-enantioselective-cross-electrophile-coupling-of-styrene-oxides-with-aryl-iodides/2022-12-30T16:44:26-08:00https://doyle.chem.ucla.edu/avada_faq/62-univariate-classification-of-phosphine-ligation-state-and-reactivity-in-cross-coupling-catalysis/2022-12-30T16:48:28-08:00https://doyle.chem.ucla.edu/avada_faq/63-phosphine-photoredox-catalyzed-anti-markovnikov-hydroamination-of-olefins-with-primary-sulfonamides-via-%ce%b1-scission-from-phosphoranyl-radicals/2022-12-30T20:30:50-08:00https://doyle.chem.ucla.edu/avada_faq/64-the-evolution-of-data-driven-modeling-in-organic-chemistry/2022-12-30T20:30:20-08:00https://doyle.chem.ucla.edu/avada_faq/65-the-open-reaction-database/2022-12-30T20:29:25-08:00https://doyle.chem.ucla.edu/avada_faq/66-a-general-strategy-for-csp3-h-functionalization-with-nucleophiles-using-methyl-radical-as-a-hydrogen-atom-abstractor/2022-12-30T20:32:18-08:00https://doyle.chem.ucla.edu/avada_faq/67-a-general-strategy-for-csp3-h-functionalization-with-nucleophiles-using-methyl-radical-as-a-hydrogen-atom-abstractor/2022-12-30T17:01:58-08:00https://doyle.chem.ucla.edu/avada_faq/68-using-data-science-to-guide-aryl-bromide-substrate-scope-analysis-in-a-ni-photoredox-catalyzed-cross-coupling-with-acetals-as-alcohol-derived-radical-sources/2022-12-30T17:04:00-08:00https://doyle.chem.ucla.edu/avada_faq/69-auto-qchem-an-automated-workflow-for-the-generation-and-storage-of-dft-calculations-for-organic-molecules/2022-12-30T17:12:18-08:00https://doyle.chem.ucla.edu/avada_faq/70-oxidative-addition-of-aryl-halides-to-a-nii-bipyridine-complex/2022-12-30T17:15:24-08:00https://doyle.chem.ucla.edu/avada_faq/71-bioinspired-supercharging-of-photoredox-catalysis-for-applications-in-energy-and-chemical-manufacturing/2022-12-30T17:27:44-08:00https://doyle.chem.ucla.edu/avada_faq/72-structure-reactivity-relationships-of-buchwald-type-phosphines-in-nickel-catalyzed-cross-couplings/2022-12-30T17:30:50-08:00https://doyle.chem.ucla.edu/avada_faq/73-ni-photoredox-catalyzed-csp3-csp3-coupling-between-aziridines-and-acetals-as-alcohol-derived-alkyl-radical-precursors/2022-12-30T17:42:21-08:00https://doyle.chem.ucla.edu/avada_faq/74-a-multi-objective-active-learning-platform-and-web-app-for-reaction-optimization/2022-12-30T17:36:45-08:00https://doyle.chem.ucla.edu/avada_faq/75-radical-redox-annulations-a-general-light-driven-method-for-the-synthesis-of-saturated-heterocycles/2022-12-30T17:39:02-08:00https://doyle.chem.ucla.edu/avada_faq/76-on-the-use-of-real-world-datasets-for-reaction-yield-prediction/2023-03-29T12:37:42-07:00https://doyle.chem.ucla.edu/avada_faq/77-a-machine-learning-approach-to-model-interaction-effects-development-and-application-to-alcohol-deoxyfluorination/2023-04-13T09:16:02-07:00https://doyle.chem.ucla.edu/avada_faq/78-interrogating-the-mechanistic-features-of-nii-mediated-aryl-iodide-oxidative-addition-using-electroanalytical-and-statistical-modeling-techniques/2023-04-25T09:16:29-07:00https://doyle.chem.ucla.edu/avada_faq/79-strategies-for-nucleophilic-csp3-radiofluorination/2023-05-31T15:56:07-07:00https://doyle.chem.ucla.edu/avada_faq/80-comparison-of-monophosphine-and-bisphosphine-precatalysts-for-ni-catalyzed-suzuki-miyaura-cross-coupling-understanding-the-role-of-the-ligation-state-in-catalysis/2023-06-05T13:39:19-07:00https://doyle.chem.ucla.edu/avada_faq/81-continuous-flow-synthesis-of-pyridinium-salts-accelerated-by-multi-objective-bayesian-optimization-with-active-learning/2024-05-27T18:31:12-07:00https://doyle.chem.ucla.edu/avada_faq/82-a-general-photocatalytic-strategy-for-nucleophilic-amination-of-primary-and-secondary-benzylic-c-h-bonds/2024-05-27T18:31:32-07:00https://doyle.chem.ucla.edu/avada_faq/83-synthesis-of-nickeli-bromide-complexes-via-oxidation-and-ligand-displacement-evaluation-of-ligand-effects-on-speciation-and-reactivity/2024-05-27T18:31:51-07:00https://doyle.chem.ucla.edu/avada_faq/84-branched-selective-cross-electrophile-coupling-of-2-alkyl-aziridines-and-heteroaryl-iodides-using-ti-ni-catalysis/2024-05-27T18:32:07-07:00https://doyle.chem.ucla.edu/avada_faq/85-dataset-design-for-building-models-of-chemical-reactivity/2024-05-27T18:32:22-07:00https://doyle.chem.ucla.edu/avada_faq/86-catalyst-deactivation-of-a-monoligated-cyjohnphos-bound-nickel0-complex/2024-05-27T18:32:36-07:00https://doyle.chem.ucla.edu/avada_faq/87-broad-survey-of-selectivity-in-the-heterogeneous-hydrogenation-of-heterocycles/2024-05-27T18:32:51-07:00https://doyle.chem.ucla.edu/avada_faq/88-identifying-general-reaction-conditions-by-bandit-optimization/2024-05-27T18:33:07-07:00https://doyle.chem.ucla.edu/avada_faq/89-data-science-guided-multiobjective-optimization-of-a-stereoconvergent-nickel-catalyzed-reduction-of-enol-tosylates-to-access-trisubstituted-alkenes/2024-05-27T18:33:20-07:00https://doyle.chem.ucla.edu/avada_faq/90-autonomous-closed-loop-mechanistic-investigation-of-molecular-electrochemistry-via-automation/2024-05-27T18:36:11-07:00https://doyle.chem.ucla.edu/avada_faq/91-mechanism-of-ni-catalyzed-photochemical-halogen-atom-mediated-csp3-h-arylation/2024-07-10T12:37:22-07:00https://doyle.chem.ucla.edu/avada_faq/92-cooperative-phosphine-photoredox-catalysis-enables-n-h-activation-of-azoles-for-intermolecular-olefin-hydroamination/2024-08-06T13:50:52-07:00https://doyle.chem.ucla.edu/avada_faq/93-multi-threshold-analysis-for-chemical-space-mapping-of-ni-catalyzed-suzuki-miyaura-couplings/2024-10-25T21:41:13-07:00https://doyle.chem.ucla.edu/avada_faq/94-data-science-driven-discovery-of-optimal-conditions-and-a-condition-selection-model-for-the-chan-lam-coupling-of-primary-sulfonamides/2025-03-25T21:35:45-07:00https://doyle.chem.ucla.edu/avada_faq/95-diversification-of-acridinium-photocatalysts-property-tuning-and-reactivity-in-model-reactions/2025-07-03T17:19:04-07:00https://doyle.chem.ucla.edu/avada_faq/96-biosourced-functional-hydroxybenzoate-co-lactide-polymers-with-antimicrobial-activity/2025-07-03T17:21:45-07:00https://doyle.chem.ucla.edu/avada_faq/97-applying-active-learning-toward-building-a-generalizable-model-for-ni-photoredox-cross-electrophile-coupling-of-aryl-and-alkyl-bromides/2025-07-03T17:23:09-07:00https://doyle.chem.ucla.edu/avada_faq/98-fabrication-of-sers-substrates-using-silver-coated-gold-nanostars-for-chemical-sensing-a-multiobjective-bayesian-optimization-approach/2025-07-03T17:24:08-07:00https://doyle.chem.ucla.edu/avada_faq/99-data-science-guided-development-of-deoxyfluorination-reagents-with-enhanced-reactivity-practicality-and-safety/2025-09-08T08:56:18-07:00https://doyle.chem.ucla.edu/avada_faq/100-ni-catalyzed-reductive-coupling-of-acetals-with-anhydrides-and-vinyl-triflates-via-single-electron-c-o-activation/2025-09-08T08:57:08-07:00https://doyle.chem.ucla.edu/avada_faq/101-light-promoted-csp%c2%b3-csp%c2%b3-reductive-elimination-from-dialkyl-niii-complexes/2026-01-24T17:38:19-08:00https://doyle.chem.ucla.edu/avada_faq/102-reactivity-studies-of-bipyridine-ligated-nickeli-and-nickel0-complexes-inform-the-mechanism-in-modern-cross-coupling-reactions/2026-01-24T17:39:03-08:00https://doyle.chem.ucla.edu/avada_faq/103-considerations-in-pursuing-reaction-scope-generality/2026-01-27T16:44:39-08:00https://doyle.chem.ucla.edu/avada_faq/104-multi-level-qtaim-enriched-graph-neural-networks-for-resolving-properties-of-transition-metal-complexes/2026-01-27T16:47:03-08:00https://doyle.chem.ucla.edu/avada_faq/105-development-application-and-mechanistic-interrogation-of-a-dual-ni-catalysis-approach-to-photoredox-based-csp3-csp3-cross-coupling/2026-01-27T16:48:15-08:00https://doyle.chem.ucla.edu/avada_faq/106-synergizing-chemical-and-ai-communities-for-advancing-laboratories-of-the-future/2026-03-21T16:45:42-07:00https://doyle.chem.ucla.edu/avada_faq/107-transferable-enantioselectivity-models-from-sparse-data/2026-05-11T23:32:14-07:00https://doyle.chem.ucla.edu/avada_faq/108-markovnikov-hydroamination-of-terminal-alkenes-via-phosphine-redox-catalysis/2026-05-11T23:32:40-07:00https://doyle.chem.ucla.edu/avada_faq/109-integrating-data-science-and-machine-learning-with-an-aldol-condensation-laboratory/2026-03-21T16:49:40-07:00https://doyle.chem.ucla.edu/avada_faq/109-integrating-data-science-and-machine-learning-with-an-aldol-condensation-laboratory-2/2026-06-03T11:45:48-07:00https://doyle.chem.ucla.edu/avada_faq/111-bunny-an-nn-bidentate-nitrogen-ligand-descriptor-library-development-and-application-to-modeling-of-ni-catalyzed-asymmetric-cross-electrophile-coupling-reactions/2026-06-03T11:44:56-07:00