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Design and Synthesis of C<sub>4</sub>‐Symmetric Axially Chiral β‐Aryl Porphyrins and Application for Supporting Ir(III)‐Catalyzed Enantioselective C−H Alkylation.
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- Angewandte Chemie, 2024, v. 136, n. 28, p. 1, doi. 10.1002/ange.202404329
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Design and Synthesis of C<sub>4</sub>‐Symmetric Axially Chiral β‐Aryl Porphyrins and Application for Supporting Ir(III)‐Catalyzed Enantioselective C−H Alkylation.
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- Angewandte Chemie International Edition, 2024, v. 63, n. 28, p. 1, doi. 10.1002/anie.202404329
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- Article
Arylative Ring Expansion of 3‐Vinylazetidin‐3‐Ols and 3‐Vinyloxetan‐3‐Ols to Dihydrofurans by Dual Palladium and Acid Catalysis.
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- Angewandte Chemie, 2024, v. 136, n. 22, p. 1, doi. 10.1002/ange.202403484
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Arylative Ring Expansion of 3‐Vinylazetidin‐3‐Ols and 3‐Vinyloxetan‐3‐Ols to Dihydrofurans by Dual Palladium and Acid Catalysis.
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- Angewandte Chemie International Edition, 2024, v. 63, n. 22, p. 1, doi. 10.1002/anie.202403484
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- Article
Benzylic C(sp<sup>3</sup>)−H Azidation: Copper vs Iron Catalysis.
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- Helvetica Chimica Acta, 2024, v. 107, n. 3, p. 1, doi. 10.1002/hlca.202400004
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- Article
Palladium‐Based Dyotropic Rearrangement Enables A Triple Functionalization of Gem‐Disubstituted Alkenes: An Unusual Fluorolactonization Reaction.
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- Angewandte Chemie, 2024, v. 136, n. 1, p. 1, doi. 10.1002/ange.202316393
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Palladium‐Based Dyotropic Rearrangement Enables A Triple Functionalization of Gem‐Disubstituted Alkenes: An Unusual Fluorolactonization Reaction.
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- Angewandte Chemie International Edition, 2024, v. 63, n. 1, p. 1, doi. 10.1002/anie.202316393
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- Article
Terminal Alkynes as One‐Carbon Donors in [5+1] Heteroannulation: Synthesis of Pyridines via Ynimine Intermediates and Application in the Total Synthesis of Anibamine B.
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- Angewandte Chemie, 2023, v. 135, n. 22, p. 1, doi. 10.1002/ange.202303537
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Terminal Alkynes as One‐Carbon Donors in [5+1] Heteroannulation: Synthesis of Pyridines via Ynimine Intermediates and Application in the Total Synthesis of Anibamine B.
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- Angewandte Chemie International Edition, 2023, v. 62, n. 22, p. 1, doi. 10.1002/anie.202303537
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Asymmetric Construction of α,α‐Disubstituted Piperazinones Enabled by Benzilic Amide Rearrangement.
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- Angewandte Chemie, 2023, v. 135, n. 18, p. 1, doi. 10.1002/ange.202217954
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Asymmetric Construction of α,α‐Disubstituted Piperazinones Enabled by Benzilic Amide Rearrangement.
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- Angewandte Chemie International Edition, 2023, v. 62, n. 18, p. 1, doi. 10.1002/anie.202217954
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- Article
Divergent Asymmetric Total Synthesis of (−)‐Voacafricines A and B.
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- Angewandte Chemie, 2023, v. 135, n. 16, p. 1, doi. 10.1002/ange.202301517
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Divergent Asymmetric Total Synthesis of (−)‐Voacafricines A and B.
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- Angewandte Chemie International Edition, 2023, v. 62, n. 16, p. 1, doi. 10.1002/anie.202301517
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- Article
Highly Strained Oxygen‐Doped Chiral Molecular Belts of the Zigzag‐Type with Strong Circularly Polarized Luminescence.
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- Angewandte Chemie, 2023, v. 135, n. 15, p. 1, doi. 10.1002/ange.202301782
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Highly Strained Oxygen‐Doped Chiral Molecular Belts of the Zigzag‐Type with Strong Circularly Polarized Luminescence.
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- Angewandte Chemie International Edition, 2023, v. 62, n. 15, p. 1, doi. 10.1002/anie.202301782
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- Article
Organocatalytic Enantioselective Pictet–Spengler Reaction of α‐Ketoesters: Development and Application to the Total Synthesis of (+)‐Alstratine A.
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- Angewandte Chemie, 2023, v. 135, n. 1, p. 1, doi. 10.1002/ange.202213831
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Organocatalytic Enantioselective Diels–Alder Reaction of 2‐Trifluoroacetamido‐1,3‐dienes with α,β‐Unsaturated Ketones.
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- Angewandte Chemie, 2023, v. 135, n. 1, p. 1, doi. 10.1002/ange.202214925
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- Article
Organocatalytic Enantioselective Pictet–Spengler Reaction of α‐Ketoesters: Development and Application to the Total Synthesis of (+)‐Alstratine A.
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- Angewandte Chemie International Edition, 2023, v. 62, n. 1, p. 1, doi. 10.1002/anie.202213831
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- Article
Organocatalytic Enantioselective Diels–Alder Reaction of 2‐Trifluoroacetamido‐1,3‐dienes with α,β‐Unsaturated Ketones.
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- Angewandte Chemie International Edition, 2023, v. 62, n. 1, p. 1, doi. 10.1002/anie.202214925
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Apparent 6‐endo‐trig Carbofluorination of Alkenes Enabled by Palladium‐Based Dyotropic Rearrangement.
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- Angewandte Chemie, 2022, v. 134, n. 50, p. 1, doi. 10.1002/ange.202211470
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Apparent 6‐endo‐trig Carbofluorination of Alkenes Enabled by Palladium‐Based Dyotropic Rearrangement.
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- Angewandte Chemie International Edition, 2022, v. 61, n. 50, p. 1, doi. 10.1002/anie.202211470
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Thiazole Boron Difluoride Dyes with Large Stokes Shift, Solid State Emission and Room‐Temperature Phosphorescence.
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- Chemistry - A European Journal, 2022, v. 28, n. 65, p. 1, doi. 10.1002/chem.202202507
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Taming the radical cation intermediate enabled one-step access to structurally diverse lignans.
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- Nature Communications, 2022, v. 13, n. 1, p. 1, doi. 10.1038/s41467-022-31000-4
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- Article
Catalytic Enantioselective Pictet–Spengler Reaction of α‐Ketoamides Catalyzed by a Single H‐Bond Donor Organocatalyst.
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- Angewandte Chemie, 2022, v. 134, n. 19, p. 1, doi. 10.1002/ange.202201788
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- Article
Catalytic Enantioselective Pictet–Spengler Reaction of α‐Ketoamides Catalyzed by a Single H‐Bond Donor Organocatalyst.
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- Angewandte Chemie International Edition, 2022, v. 61, n. 19, p. 1, doi. 10.1002/anie.202201788
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- Article
Copper‐Catalyzed Aza‐Sonogashira Cross‐Coupling To Form Ynimines: Development and Application to the Synthesis of Heterocycles.
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- Angewandte Chemie, 2021, v. 133, n. 45, p. 24230, doi. 10.1002/ange.202110901
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Copper‐Catalyzed Aza‐Sonogashira Cross‐Coupling To Form Ynimines: Development and Application to the Synthesis of Heterocycles.
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- Angewandte Chemie International Edition, 2021, v. 60, n. 45, p. 24028, doi. 10.1002/anie.202110901
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Enantioselective Total Synthesis of (+)‐Nordasycarpidone, (+)‐Dasycarpidone, and (+)‐Uleine.
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- Helvetica Chimica Acta, 2021, v. 104, n. 8, p. 1, doi. 10.1002/hlca.202100088
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Enantioselective Total Synthesis of (+)‐Alstilobanine C, (+)‐Undulifoline, and (−)‐Alpneumine H.
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- Angewandte Chemie, 2021, v. 133, n. 22, p. 12500, doi. 10.1002/ange.202103580
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Enantioselective Total Synthesis of (+)‐Alstilobanine C, (+)‐Undulifoline, and (−)‐Alpneumine H.
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- Angewandte Chemie International Edition, 2021, v. 60, n. 22, p. 12392, doi. 10.1002/anie.202103580
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Iron-Catalysed Remote C(sp3 )-H Azidation of O-Acyl Oximes and N-Acyloxy Imidates.
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- Chimia, 2021, v. 75, n. 4, p. 329, doi. 10.2533/chimia.2021.329
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Catalytic Enantioselective Aminopalladation–Heck Cascade.
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- Angewandte Chemie, 2021, v. 133, n. 13, p. 7169, doi. 10.1002/ange.202016001
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Catalytic Enantioselective Aminopalladation–Heck Cascade.
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- Angewandte Chemie International Edition, 2021, v. 60, n. 13, p. 7093, doi. 10.1002/anie.202016001
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Selective 1,2‐Aminoisothiocyanation of 1,3‐Dienes Under Visible‐Light Photoredox Catalysis.
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- Angewandte Chemie, 2021, v. 133, n. 8, p. 4131, doi. 10.1002/ange.202014518
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Selective 1,2‐Aminoisothiocyanation of 1,3‐Dienes Under Visible‐Light Photoredox Catalysis.
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- Angewandte Chemie International Edition, 2021, v. 60, n. 8, p. 4085, doi. 10.1002/anie.202014518
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Unified divergent strategy towards the total synthesis of the three sub-classes of hasubanan alkaloids.
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- Nature Communications, 2021, v. 12, n. 1, p. 1, doi. 10.1038/s41467-020-20274-1
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- Article
Radical‐Cation Cascade to Aryltetralin Cyclic Ether Lignans Under Visible‐Light Photoredox Catalysis.
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- Angewandte Chemie, 2020, v. 132, n. 47, p. 21381, doi. 10.1002/ange.202007548
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Radical‐Cation Cascade to Aryltetralin Cyclic Ether Lignans Under Visible‐Light Photoredox Catalysis.
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- Angewandte Chemie International Edition, 2020, v. 59, n. 47, p. 21195, doi. 10.1002/anie.202007548
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- Article
TiCl<sub>3</sub>‐Mediated Synthesis of 2,3,3‐Trisubstituted Indolenines: Total Synthesis of (+)‐1,2‐Dehydroaspidospermidine, (+)‐Condyfoline, and (−)‐Tubifoline.
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- Angewandte Chemie, 2020, v. 132, n. 33, p. 14094, doi. 10.1002/ange.202005380
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TiCl<sub>3</sub>‐Mediated Synthesis of 2,3,3‐Trisubstituted Indolenines: Total Synthesis of (+)‐1,2‐Dehydroaspidospermidine, (+)‐Condyfoline, and (−)‐Tubifoline.
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- Angewandte Chemie International Edition, 2020, v. 59, n. 33, p. 13990, doi. 10.1002/anie.202005380
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Synthesis of Benzo[a]carbazoles through Visible Light‐Induced Cycloaromatization.
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- Helvetica Chimica Acta, 2020, v. 103, n. 8, p. 1, doi. 10.1002/hlca.202000106
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Copper‐Catalyzed Cyanoalkylative Aziridination of N‐Sulfonyl Allylamines.
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- Advanced Synthesis & Catalysis, 2020, v. 362, n. 11, p. 2205, doi. 10.1002/adsc.202000276
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Catalytic Enantioselective Benzilic Ester Rearrangement.
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- Angewandte Chemie, 2020, v. 132, n. 18, p. 7328, doi. 10.1002/ange.202001258
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Catalytic Enantioselective Benzilic Ester Rearrangement.
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- Angewandte Chemie International Edition, 2020, v. 59, n. 18, p. 7261, doi. 10.1002/anie.202001258
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- Article
Towards the Sarpagine‐Ajmaline‐Macroline Family of Indole Alkaloids: Enantioselective Synthesis of an N‐Demethyl Alstolactone Diastereomer.
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- Chemistry - A European Journal, 2020, v. 26, n. 21, p. 4866, doi. 10.1002/chem.202000415
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Palladium‐Catalyzed Enantioselective Cacchi Reaction: Asymmetric Synthesis of Axially Chiral 2,3‐Disubstituted Indoles.
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- Angewandte Chemie, 2020, v. 132, n. 5, p. 2121, doi. 10.1002/ange.201914049
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Palladium‐Catalyzed Enantioselective Cacchi Reaction: Asymmetric Synthesis of Axially Chiral 2,3‐Disubstituted Indoles.
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- Angewandte Chemie International Edition, 2020, v. 59, n. 5, p. 2105, doi. 10.1002/anie.201914049
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Functionalization of remote C(sp3)-H bonds enabled by copper-catalyzed coupling of O-acyloximes with terminal alkynes.
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- Nature Communications, 2020, v. 11, n. 1, p. 1, doi. 10.1038/s41467-020-14292-2
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Fused N‐Heterocycles with Contiguous Stereogenic Centers Accessed by an Asymmetric Catalytic Cascade Reaction of Tertiary Enamides.
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- Chemistry - A European Journal, 2020, v. 26, n. 2, p. 401, doi. 10.1002/chem.201904596
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Remote C(sp<sup>3</sup>)−H Arylation and Vinylation of N‐Alkoxypyridinium Salts to δ‐Aryl and δ‐Vinyl Alcohols.
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- Chemistry - A European Journal, 2019, v. 25, n. 50, p. 11630, doi. 10.1002/chem.201902918
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- Article