Mechanistic Features of Asymmetric Vinylidene ortho-Quinone Methide Construction and Subsequent Transformations
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[1] Jie Chen,et al. Modular Construction of Heterobiaryl Atropisomers and Axially Chiral Styrenes via All-Carbon Tetrasubstituted VQMs. , 2022, Angewandte Chemie.
[2] Xingguang Li,et al. Quinone methides and indole imine methides as intermediates in enantioselective catalysis , 2022, Nature Synthesis.
[3] Hailong Yan,et al. Organocatalytic atroposelective construction of axially chiral N, N- and N, S-1,2-azoles through novel ring formation approach , 2022, Nature Communications.
[4] C. Tung,et al. Asymmetric Azide-Alkyne Cycloaddition with Ir(I)/Squaramide Cooperative Catalysis: Atroposelective Synthesis of Axially Chiral Aryltriazoles. , 2022, Journal of the American Chemical Society.
[5] Hailong Yan,et al. An Isolable Vinylidene ortho-Quinone Methide: Synthesis, Structure and Reactivity. , 2022, Angewandte Chemie.
[6] Ying He,et al. P-stereogenic N-vinylphosphonamides enabled by asymmetric allylic substitution-isomerization , 2021, Cell Reports Physical Science.
[7] Hailong Yan,et al. Diversity-oriented enantioselective construction of atropisomeric heterobiaryls and N-aryl indoles via vinylidene ortho-quinone methides (VQMs) , 2021 .
[8] Hailong Yan,et al. Organocatalytic enantioselective construction of chiral azepine skeleton bearing multiple-stereogenic elements. , 2021, Angewandte Chemie.
[9] Ying He,et al. Tandem Iridium Catalysis as a General Strategy for Atroposelective Construction of Axially Chiral Styrenes. , 2021, Journal of the American Chemical Society.
[10] K. Tan,et al. Enantioselective Synthesis of Axially Chiral Biaryls by Diels-Alder/Retro-Diels-Alder Reaction of 2-Pyrones with Alkynes. , 2021, Journal of the American Chemical Society.
[11] D. Wei,et al. Insights into the chiral sulfide/selenide-catalyzed electrophilic carbothiolation of alkynes: mechanism and origin of axial chirality , 2021 .
[12] D. Wei,et al. Origin and stabilization of axial chirality in the construction of naphthyl-C2-indoles: a DFT study , 2020 .
[13] Chao‐Jun Li,et al. Coupling without Coupling Reactions: En Route to Developing Phenols as Sustainable Coupling Partners via Dearomatization-Rearomatization Processes. , 2020, Accounts of chemical research.
[14] P. Liu,et al. Asymmetric allylic substitution–isomerization to axially chiral enamides via hydrogen-bonding assisted central-to-axial chirality transfer† , 2020, Chemical science.
[15] B. Tan,et al. Design and Atroposelective Construction of IAN analogues via Organocatalytic Asymmetric Heteroannulation of Alkynes. , 2020, Angewandte Chemie.
[16] Hailong Yan,et al. N-Iodosuccinimide-Mediated Dimerization of 2-Alkynylnaphthols: A Highly Diastereoselective Construction of Bridged Polycyclic Compounds via Vinylidene ortho-Quinone Methide Intermediate. , 2020, Organic letters.
[17] Hailong Yan,et al. Enantioselective control of both helical and axial stereogenic elements via an organocatalytic approach. , 2019, Angewandte Chemie.
[18] Hailong Yan,et al. Organocatalytic Asymmetric Annulation of ortho-Alkynylanilines: Synthesis of Axially Chiral Naphthyl-C2-Indoles. , 2019, Angewandte Chemie.
[19] A. Matsumoto,et al. Enantioselective bromination of axially chiral cyanoarenes in the presence of bifunctional organocatalysts , 2019, RSC advances.
[20] Jean Rodriguez,et al. Enantioselective organocatalytic activation of vinylidene-quinone methides (VQMs). , 2019, Chemical communications.
[21] Hailong Yan,et al. Hydrogen-bond-induced chiral axis construction: theoretical study of cinchonine-thiourea-catalyzed enantioselective intramolecular cycloaddition. , 2019, Chemistry, an Asian journal.
[22] K. Houk,et al. Rational design, enantioselective synthesis and catalytic applications of axially chiral EBINOLs , 2019, Nature Catalysis.
[23] Yanli Zhao,et al. Catalytic asymmetric acetalization of carboxylic acids for access to chiral phthalidyl ester prodrugs , 2019, Nature Communications.
[24] R. Raines,et al. Esterification Delivers a Functional Enzyme into a Human Cell. , 2019, ACS chemical biology.
[25] Hailong Yan,et al. Asymmetric One-Pot Construction of Three Stereogenic Elements: Chiral Carbon Center, Stereoisomeric Alkenes, and Chirality of Axial Styrenes. , 2018, Organic letters.
[26] C. Nielsen,et al. Visual kinetic analysis† †Electronic supplementary information (ESI) available: Microsoft Excel files with tutorials for VTNA and RPKA and a video available at https://youtu.be/5ORFRB4U10s. See DOI: 10.1039/c8sc04698k , 2018, Chemical science.
[27] Hailong Yan,et al. Organocatalytic Asymmetric One-Step Desymmetrizing Dearomatization Reaction of Indoles: Development and Bioactivity Evaluation. , 2018, Angewandte Chemie.
[28] Hailong Yan,et al. Enantioselective Construction of Vicinal Diaxial Styrenes and Multiaxis System via Organocatalysis. , 2018, Journal of the American Chemical Society.
[29] Hailong Yan,et al. Organocatalytic Atroposelective Intramolecular [4+2] Cycloaddition: Synthesis of Axially Chiral Heterobiaryls. , 2018, Angewandte Chemie.
[30] Hailong Yan,et al. Organocatalytic Enantioselective Construction of Axially Chiral Sulfone-Containing Styrenes. , 2018, Journal of the American Chemical Society.
[31] Kazunobu Igawa,et al. Vinylidene ortho-Quinone Methides: Unique Chiral Reaction Intermediates in Catalytic Asymmetric Synthesis. , 2018, Chimia.
[32] Hailong Yan,et al. Organocatalytic Intramolecular [4+2] Cycloaddition between In Situ Generated Vinylidene ortho-Quinone Methides and Benzofurans. , 2017, Angewandte Chemie.
[33] R. Raines,et al. Cytosolic Delivery of Proteins by Bioreversible Esterification. , 2017, Journal of the American Chemical Society.
[34] J. Burés. Variable Time Normalization Analysis: General Graphical Elucidation of Reaction Orders from Concentration Profiles. , 2016, Angewandte Chemie.
[35] H. Schaefer,et al. Electrophilic Aromatic Substitution: New Insights into an Old Class of Reactions. , 2016, Accounts of chemical research.
[36] Rai‐Shung Liu,et al. Recent Advances in Gold-Catalyzed N- and O-Functionalizations of Alkynes with Nitrones, Nitroso, Nitro and Nitroxy Species , 2016 .
[37] J. Burés. A Simple Graphical Method to Determine the Order in Catalyst , 2016, Angewandte Chemie.
[38] K. Asano,et al. Bifunctional organocatalysts for the enantioselective synthesis of axially chiral isoquinoline N-oxides. , 2015, Journal of the American Chemical Society.
[39] T. Hashimoto,et al. Recent advances of catalytic asymmetric 1,3-dipolar cycloadditions. , 2015, Chemical reviews.
[40] T. Poulsen,et al. Ester coupling reactions--an enduring challenge in the chemical synthesis of bioactive natural products. , 2015, Natural product reports.
[41] Kun-Liang Wu,et al. The Domestication of ortho-Quinone Methides , 2014, Accounts of chemical research.
[42] Jeffrey S. Johnson,et al. Dynamic kinetic asymmetric transformations of β-stereogenic α-ketoesters by direct aldolization. , 2014, Angewandte Chemie.
[43] A. Sakakura,et al. Enantioselective cyanoethoxycarbonylation of isatins promoted by a Lewis base-Brønsted acid cooperative catalyst. , 2013, Angewandte Chemie.
[44] T. Kimachi,et al. Organocatalyzed Isomerization of α‐Substituted Alkynoates into Trisubstituted Allenoates by Dynamic Kinetic Resolution , 2012 .
[45] F. Doria,et al. Vinylidene-quinone methides, photochemical generation and β-silicon effect on reactivity. , 2012, The Journal of organic chemistry.
[46] K. Matsuzaki,et al. Bifunctional hydrogen-bond donors that bear a quinazoline or benzothiadiazine skeleton for asymmetric organocatalysis. , 2011, Chemistry.
[47] H. Pellissier. Organocatalyzed Dynamic Kinetic Resolution , 2011 .
[48] Scott J. Miller,et al. Dynamic Kinetic Resolution of Biaryl Atropisomers via Peptide-Catalyzed Asymmetric Bromination , 2010, Science.
[49] C. K. Andrade,et al. 3-arylamino and 3-alkoxy-nor-beta-lapachone derivatives: synthesis and cytotoxicity against cancer cell lines. , 2010, Journal of medicinal chemistry.
[50] Lili Lin,et al. Amide-based bifunctional organocatalysts in asymmetric reactions. , 2009, Chemical communications.
[51] C. Song. Cinchona Alkaloids in Synthesis and Catalysis , 2009 .
[52] Xinhong Yu,et al. Hydrogen-bond-mediated asymmetric catalysis. , 2008, Chemistry, an Asian journal.
[53] F. Zaera,et al. Competitive chemisorption between pairs of cinchona alkaloids and related compounds from solution onto platinum surfaces. , 2006, Journal of the American Chemical Society.
[54] Mark S. Taylor,et al. Asymmetric catalysis by chiral hydrogen-bond donors. , 2006, Angewandte Chemie.
[55] Suaib Luqman,et al. Synthesis of 1-(3',4',5'-trimethoxy) phenyl naphtho[2,1b]furan as a novel anticancer agent. , 2006, Bioorganic & medicinal chemistry letters.
[56] E. Vedejs,et al. Efficiency in nonenzymatic kinetic resolution. , 2005, Angewandte Chemie.
[57] K. Fukumoto,et al. A convenient method for the preparation of inverted tert-alkyl carboxylates from chiral tert-alcohols by a new type of oxidation-reduction condensation using 2,6-dimethyl-1,4-benzoquinone. , 2003, Journal of the American Chemical Society.
[58] A. Baiker,et al. Asymmetric hydrogenation on platinum: nonlinear effect of coadsorbed cinchona alkaloids on enantiodifferentiation , 2003 .
[59] O. Mitsunobu. The Use of Diethyl Azodicarboxylate and Triphenylphosphine in Synthesis and Transformation of Natural Products , 1981 .