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Total Synthesis of the Euphorbia Diterpenoid Pepluacetal.
- Published in:
- Angewandte Chemie, 2024, v. 136, n. 21, p. 1, doi. 10.1002/ange.202400943
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- Article
Total Synthesis of the Euphorbia Diterpenoid Pepluacetal.
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- Angewandte Chemie International Edition, 2024, v. 63, n. 21, p. 1, doi. 10.1002/anie.202400943
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- Article
Synthesis of Spiro[4.5]ecanes by Au(I)‐Catalyzed Vinylogous Conia Ene Reaction.
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- European Journal of Organic Chemistry, 2024, v. 27, n. 4, p. 1, doi. 10.1002/ejoc.202301202
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Solvent‐free, B(C<sub>6</sub>F<sub>5</sub>)<sub>3</sub>‐Catalyzed S−H Insertion of Thiophenols and Thiols with α‐Diazoesters.
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- Chemistry - An Asian Journal, 2022, v. 17, n. 16, p. 1, doi. 10.1002/asia.202200465
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- Article
Collective Total Syntheses of Five Lycopodium Alkaloids.
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- Angewandte Chemie, 2022, v. 134, n. 32, p. 1, doi. 10.1002/ange.202205439
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Collective Total Syntheses of Five Lycopodium Alkaloids.
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- Angewandte Chemie International Edition, 2022, v. 61, n. 32, p. 1, doi. 10.1002/anie.202205439
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- Article
Enantioselective Pictet–Spengler Condensation to Access the Total Synthesis of (+)‐Tabertinggine.
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- European Journal of Organic Chemistry, 2022, v. 2022, n. 10, p. 1, doi. 10.1002/ejoc.202200088
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- Article
Concise Total Syntheses of Bioactive Alkaloids Enabled by Development or Application of Cascade Reactions: A Personnel Adventure.
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- Chinese Journal of Chemistry, 2021, v. 39, n. 4, p. 795, doi. 10.1002/cjoc.202000522
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- Article
Frontispiece: The Total Synthesis of Diquinane‐Containing Natural Products.
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- Chemistry - A European Journal, 2021, v. 27, n. 15, p. 1, doi. 10.1002/chem.202181564
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The Total Synthesis of Diquinane‐Containing Natural Products.
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- Chemistry - A European Journal, 2021, v. 27, n. 15, p. 4839, doi. 10.1002/chem.202003741
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- Article
Total Synthesis of (−)‐Pepluanol B: Conformational Control of the Eight‐Membered‐Ring System.
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- Angewandte Chemie, 2020, v. 132, n. 10, p. 3994, doi. 10.1002/ange.201915876
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- Article
Total Synthesis of (−)‐Pepluanol B: Conformational Control of the Eight‐Membered‐Ring System.
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- Angewandte Chemie International Edition, 2020, v. 59, n. 10, p. 3966, doi. 10.1002/anie.201915876
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- Article
An Efficient Synthesis of Benzazocines by Gold(I)-Catalyzed Tandem 1,2-Acyloxy Shift/[3+2] Cycloaddition of Terminal 1,9-Enynyl Esters.
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- Chemistry - An Asian Journal, 2016, v. 11, n. 15, p. 2167, doi. 10.1002/asia.201600593
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- Article
Concise Total Synthesis of the Bisnorditerpene (+)-(5β,8α,10α)-8-hydroxy-13-methylpodocarpa-9(11),13-diene-3,12-dione.
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- Asian Journal of Organic Chemistry, 2016, v. 5, n. 8, p. 986, doi. 10.1002/ajoc.201600209
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- Article
Bioinspired Total Syntheses of Isospongian-type Diterpenoids (−)-Kravanhins A and C.
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- Chemistry - An Asian Journal, 2016, v. 11, n. 10, p. 1542, doi. 10.1002/asia.201600398
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- Article
An Upstream By-product from Ester Activation via NHC-Catalysis Catalyzes Downstream Sulfonyl Migration Reaction.
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- Chemistry - An Asian Journal, 2016, v. 11, n. 2, p. 193, doi. 10.1002/asia.201500959
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- Article
Gold(I)-Catalyzed Tandem Reaction of γ-Amino-Substituted Propargylic Esters to Pyrrolines and its Application in the Formal Synthesis of (±)-Aphanorphine.
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- Advanced Synthesis & Catalysis, 2015, v. 357, n. 9, p. 2082, doi. 10.1002/adsc.201401161
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Gold-Catalyzed 1,2-Acyloxy Migration/Intramolecular [3+2] 1,3-Dipolar Cycloaddtion Cascade Reaction: An Efficient Strategy for Syntheses of Medium-Sized-Ring Ethers and Amines.
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- Angewandte Chemie, 2014, v. 126, n. 40, p. 10965, doi. 10.1002/ange.201406486
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- Article
Gold-Catalyzed 1,2-Acyloxy Migration/Intramolecular [3+2] 1,3-Dipolar Cycloaddtion Cascade Reaction: An Efficient Strategy for Syntheses of Medium-Sized-Ring Ethers and Amines.
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- Angewandte Chemie International Edition, 2014, v. 53, n. 40, p. 10789, doi. 10.1002/anie.201406486
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- Article
Diels-Alder/Oxidative Aromatization Approach towards the All-Carbon DEF Tricyclic Skeleton of Daphenylline.
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- Chemistry - An Asian Journal, 2014, v. 9, n. 5, p. 1274, doi. 10.1002/asia.201400002
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- Article
Concise.
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- Chemistry - An Asian Journal, 2013, v. 8, n. 7, p. 1391, doi. 10.1002/asia.201300332
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PtCl<sub>2</sub>-Catalyzed Tandem Enyne Cyclization/1,2 Ester Migration Reaction Controlled by Substituent Effects of All-Carbon 1,6-Enynyl Esters.
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- Chemistry - An Asian Journal, 2013, v. 8, n. 5, p. 892, doi. 10.1002/asia.201300018
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- Article
N-Heterocyclic Carbene (NHC)-Catalyzed/Lewis Acid Mediated Conjugate Umpolung of Alkynyl Aldehydes for the Synthesis of Butenolides: A Formal [3+2] Annulation.
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- Chemistry - A European Journal, 2013, v. 19, n. 13, p. 4146, doi. 10.1002/chem.201204386
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- Article
Concise Formal Syntheses of the Amaryllidaceae Alkaloids (±)-Tazettine and (±)-6a-Epipretazettine: Construction of the Core Skeleton via Tandem Intramolecular Oxidative Friedel-Crafts/Aza-Michael Reaction.
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- Chemistry - An Asian Journal, 2013, v. 8, n. 2, p. 364, doi. 10.1002/asia.201200964
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- Article
Rapid Construction of the [6-6-6-5] Tetracyclic Skeleton of the Daphniphyllum Alkaloid Daphenylline.
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- Chemistry - An Asian Journal, 2012, v. 7, n. 11, p. 2519, doi. 10.1002/asia.201200625
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- Article
Asymmetric Syntheses of (−)-Pentazocine and (−)-Eptazocine through an Aza-Prins Cyclization.
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- Chemistry - An Asian Journal, 2012, v. 7, n. 11, p. 2543, doi. 10.1002/asia.201200505
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- Article
Total Synthesis of (±)-Kopsihainanine A.
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- Chemistry - A European Journal, 2012, v. 18, n. 22, p. 6729, doi. 10.1002/chem.201200867
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- Article
A Concise Synthesis of (±)-Yaequinolone A2.
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- Chinese Journal of Chemistry, 2009, v. 27, n. 7, p. 1379, doi. 10.1002/cjoc.200990230
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- Article
Total Synthesis of (+)-Machaeriol D with a Key Regio- and Stereoselective SN2′ ReactionWe are grateful for the financial support of the NSFC (No. 20572036, QT program), the Special Doctorial Program Funds of the Ministry of Education of China (20040730008), GanSu Science Foundation (No. 3ZS051A25-004), and the Key Grant Project of the Ministry of Education of China (No.105169).
- Published in:
- Angewandte Chemie, 2006, v. 118, n. 22, p. 3733, doi. 10.1002/ange.200600006
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- Article
Total Synthesis of (+)-Machaeriol D with a Key Regio- and Stereoselective SN2′ ReactionWe are grateful for the financial support of the NSFC (No. 20572036, QT program), the Special Doctorial Program Funds of the Ministry of Education of China (20040730008), GanSu Science Foundation (No. 3ZS051A25-004), and the Key Grant Project of the Ministry of Education of China (No.105169).
- Published in:
- Angewandte Chemie International Edition, 2006, v. 45, n. 22, p. 3651, doi. 10.1002/anie.200600006
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- Article