Search Results - "Alexy, Eric J."
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Catalytic Enantioselective Synthesis of Acyclic Quaternary Centers: Palladium-Catalyzed Decarboxylative Allylic Alkylation of Fully Substituted Acyclic Enol Carbonates
Published in Journal of the American Chemical Society (15-08-2018)“…The first enantioselective palladium-catalyzed decarboxylative allylic alkylation of fully substituted acyclic enol carbonates providing linear α-quaternary…”
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Palladium-catalyzed enantioselective decarboxylative allylic alkylation of fully substituted N -acyl indole-derived enol carbonates
Published in Chemical science (Cambridge) (21-06-2019)“…The first enantioselective palladium-catalyzed decarboxylative allylic alkylation of fully substituted -acyl indole-derived enol carbonates forming acyclic…”
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3
Tailoring Panchromatic Absorption and Excited-State Dynamics of Tetrapyrrole–Chromophore (Bodipy, Rylene) ArraysInterplay of Orbital Mixing and Configuration Interaction
Published in Journal of the American Chemical Society (06-12-2017)“…Three sets of tetrapyrrole–chromophore arrays have been examined that exhibit panchromatic absorption across large portions of the near-ultraviolet (NUV) to…”
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Palladium-Catalyzed Enantioselective Decarboxylative Allylic Alkylation of Acyclic α- N -Pyrrolyl/Indolyl Ketones
Published in Organic letters (05-06-2020)“…The synthesis of fully substituted α- -pyrrolyl and indolyl ketones via enantioselective palladium-catalyzed allylic alkylation is described. The acyclic…”
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Enantioselective γ‑Alkylation of α,β-Unsaturated Malonates and Ketoesters by a Sequential Ir-Catalyzed Asymmetric Allylic Alkylation/Cope Rearrangement
Published in Journal of the American Chemical Society (27-04-2016)“…A catalytic, enantioselective γ-alkylation of α,β-unsaturated malonates and ketoesters is reported. This strategy entails a highly regio- and enantioselective…”
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Asymmetric Total Synthesis of Havellockate
Published in Journal of the American Chemical Society (09-11-2022)“…The first total synthesis of the furanobutenolide-derived cembranoid diterpenoid havellockate is disclosed. Our convergent strategy employs a Julia–Kocienski…”
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Palladium‐Catalyzed Enantioselective Decarboxylative Allylic Alkylation of Protected Benzoin‐Derived Enol Carbonates
Published in Advanced synthesis & catalysis (23-01-2020)“…The enantioselective palladium‐catalyzed decarboxylative allylic alkylation of fully substituted α‐hydroxy acyclic enol carbonates providing tetrasubstituted…”
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Global Diastereoconvergence in the Ireland–Claisen Rearrangement of Isomeric Enolates: Synthesis of Tetrasubstituted α‑Amino Acids
Published in Journal of the American Chemical Society (30-12-2020)“…A dual experimental/theoretical investigation of the Ireland–Claisen rearrangement of tetrasubstituted α-phthalimido ester enolates to afford…”
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Enantioselective Pd-Catalyzed Decarboxylative Allylic Alkylation of Thiopyranones. Access to Acyclic, Stereogenic α‑Quaternary Ketones
Published in Organic letters (06-10-2017)“…A catalytic, enantioselective decarboxylative allylic alkylation of 4-thiopyranones is reported. The α-quaternary 4-thiopyranones produced are challenging to…”
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Stereospecific Overman Rearrangement of Substituted Cyclic Vinyl Bromides: Access to Fully Substituted α‑Amino Ketones
Published in Organic letters (15-11-2019)“…A versatile thermal Overman rearrangement of enantioenriched, cyclic allylic alcohols providing tertiary allylic amines has been developed. The vinyl bromide…”
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Palladium-catalyzed α,β-dehydrogenation of acyclic ester equivalents promoted by a novel electron deficient phosphinooxazoline ligand
Published in Tetrahedron (02-08-2019)“…A unique example of Pd-catalyzed decarboxylative dehydrogenation of fully substituted N-acyl allyl enol carbonates is enabled by a new electron deficient…”
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12
Origin of Panchromaticity in Multichromophore–Tetrapyrrole Arrays
Published in The journal of physical chemistry. A, Molecules, spectroscopy, kinetics, environment, & general theory (13-09-2018)“…Panchromatic absorbers that have robust photophysical properties enable new designs for molecular-based light-harvesting systems. Herein, we report…”
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Paley's watchmaker analogy and prebiotic synthetic chemistry in surfactant assemblies. Formaldehyde scavenging by pyrroles leading to porphyrins as a case study
Published in Organic & biomolecular chemistry (21-10-2015)“…The formation of elaborate molecules is regarded as an essential first step in prebiotic chemistry, but how such transformations could spontaneously occur,…”
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Tuning the Electronic Structure and Properties of Perylene–Porphyrin–Perylene Panchromatic Absorbers
Published in The journal of physical chemistry. A, Molecules, spectroscopy, kinetics, environment, & general theory (29-09-2016)“…Light-harvesting architectures that afford strong absorption across the near-ultraviolet to near-infrared region, namely, panchromatic absorptivity, are…”
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Palladium-catalyzed enantioselective decarboxylative allylic alkylation of fully substituted N-acyl indole-derived enol carbonates† †Electronic supplementary information (ESI) available: Experimental procedures, NMR and IR spectra, SFC traces, X-ray crystallographic data. CCDC 1908785. For ESI and crystallographic data in CIF or other electronic format see DOI: 10.1039/c9sc01726g
Published in Chemical science (Cambridge) (17-05-2019)“…The first enantioselective Pd-catalyzed decarboxylative allylic alkylation of fully substituted N -acyl indole-derived enol carbonates generates acyclic…”
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Development of Enantioselective Transition-Metal Catalyzed Allylic Alkylation Methodologies
Published 01-01-2020“…Research in the Stoltz group is directed, generally, at the development of synthetic methods for the preparation of stereochemically rich molecules, and the…”
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Dissertation -
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Palladium-catalyzed enantioselective decarboxylative allylic alkylation of fully substituted -acyl indole-derived enol carbonates
Published in Chemical science (Cambridge) (12-06-2019)“…The first enantioselective palladium-catalyzed decarboxylative allylic alkylation of fully substituted N -acyl indole-derived enol carbonates forming acyclic…”
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