Unveiling the impact of the light-source and steric factors on [2+2] heterocycloaddition reactions
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Elisa Fresch | E. Collini | M. Natali | L. Dell’Amico | M. Bonchio | Andrea Sartorel | F. Rigodanza | Paolo Costa | J. Mateos | Alberto Vega‐Peñaloza
[1] I. Guzei,et al. Cooperative Stereoinduction in Asymmetric Photocatalysis. , 2022, Journal of the American Chemical Society.
[2] L. Dell’Amico,et al. Unlocking the Synthetic Potential of Light-Excited Aryl Ketones: Applications in Direct Photochemistry and Photoredox Catalysis , 2021, Synlett.
[3] Claudia A. Contreras-Celedón,et al. Deep Eutectic Solvent Choline Chloride/p-toluenesulfonic Acid and Water Favor the Enthalpy-Driven Binding of Arylamines to Maleimide in Aza-Michael Addition. , 2020, The Journal of organic chemistry.
[4] L. Dell’Amico,et al. Microfluidic Visible‐Light Paternò–Büchi Reaction of Oxindole Enol Ethers , 2020 .
[5] Jian Zheng,et al. Divergent Photocatalytic Reactions of α-Ketoesters under Triplet Sensitization and Photoredox Conditions. , 2020, Organic letters.
[6] L. Dell’Amico,et al. A visible-light Paternò–Büchi dearomatisation process towards the construction of oxeto-indolinic polycycles† , 2020, Chemical science.
[7] P. Melchiorre,et al. Synthetic Methods Driven by the Photoactivity of Electron Donor–Acceptor Complexes , 2020, Journal of the American Chemical Society.
[8] Z. Ouyang,et al. Visible-Light Driven [2+2] Photocycloadditions between Benzophenone and C=C Bonds in Unsaturated Lipids. , 2020, Journal of the American Chemical Society.
[9] M. D’Auria. The Paternò–Büchi reaction –a comprehensive review , 2019, Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology.
[10] Paolo Melchiorre,et al. Mechanistic Studies in Photocatalysis. , 2019, Angewandte Chemie.
[11] R. Crespo‐Otero,et al. Switching the Spin State of Pentafluorophenylnitrene: Isolation of a Singlet Arylnitrene Complex. , 2018, Journal of the American Chemical Society.
[12] T. Carofiglio,et al. A microfluidic photoreactor enables 2-methylbenzophenone light-driven reactions with superior performance. , 2018, Chemical communications.
[13] Tadashi Mori,et al. Entropy-Driven Diastereoselectivity Improvement in the Paternò-Büchi Reaction of 1-Naphthyl Aryl Ethenes with a Chiral Cyanobenzoate through Remote Alkylation. , 2018, Angewandte Chemie.
[14] N. Hoffmann,et al. The Paternò-Büchi reaction—Mechanisms and application to organic synthesis , 2017 .
[15] K. F. Morgan,et al. Oxetanes: Recent Advances in Synthesis, Reactivity, and Medicinal Chemistry. , 2016, Chemical reviews.
[16] D. MacMillan,et al. Photoredox Catalysis in Organic Chemistry , 2016, The Journal of organic chemistry.
[17] T. Bach,et al. Recent Advances in the Synthesis of Cyclobutanes by Olefin [2 + 2] Photocycloaddition Reactions , 2016, Chemical reviews.
[18] Volker Hessel,et al. Applications of Continuous-Flow Photochemistry in Organic Synthesis, Material Science, and Water Treatment. , 2016, Chemical reviews.
[19] Igor D. Jurberg,et al. X-ray characterization of an electron donor-acceptor complex that drives the photochemical alkylation of indoles. , 2015, Angewandte Chemie.
[20] Y. Aoki,et al. Exciplex ensemble modulated by excitation mode in intramolecular charge-transfer dyad: effects of temperature, solvent polarity, and wavelength on photochemistry and photophysics of tethered naphthalene-dicyanoethene system. , 2014, Organic letters.
[21] D. Maiti,et al. Ni(II)—Salt Catalyzed Activation of Primary Amine‐sp3Cα—H and Cyclization with 1,2‐Diketone to Tetrasubstituted Imidazoles. , 2014 .
[22] Tadashi Mori,et al. Charge-transfer excitation: unconventional yet practical means for controlling stereoselectivity in asymmetric photoreactions. , 2013, Chemical Society reviews.
[23] Matthew S Sigman,et al. Multidimensional steric parameters in the analysis of asymmetric catalytic reactions. , 2012, Nature chemistry.
[24] Tadashi Mori,et al. Solvent and temperature effects on diastereodifferentiating Paternó-Büchi reaction of chiral alkyl cyanobenzoates with diphenylethene upon direct versus charge-transfer excitation. , 2010, The Journal of organic chemistry.
[25] M. A. Ischay,et al. Visible light photocatalysis as a greener approach to photochemical synthesis. , 2010, Nature chemistry.
[26] B. Trost,et al. Cyclic 1,2-diketones as core building blocks: a strategy for the total synthesis of (-)-terpestacin. , 2010, Chemistry.
[27] Tadashi Mori,et al. Wavelength control of diastereodifferentiating Paterno-Buchi reaction of chiral cyanobenzoates with diphenylethene through direct versus charge-transfer excitation. , 2009, Journal of the American Chemical Society.
[28] M. Sigman,et al. Examination of the role of Taft-type steric parameters in asymmetric catalysis. , 2009, The Journal of organic chemistry.
[29] S. Bondock,et al. Selectivity control in electron spin inversion processes: regio- and stereochemistry of Paternò-Büchi photocycloadditions as a powerful tool for mapping intersystem crossing processes. , 2004, Accounts of chemical research.
[30] Tadashi Mori,et al. Diastereoselective [2 + 2] photocycloaddition of stilbene to chiral fumarate. Direct versus charge-transfer excitation. , 2004, Journal of the American Chemical Society.
[31] Ajaya K. Singh,et al. Conformational relaxation dynamics in the excited electronic states of benzil in solution , 2002 .
[32] H. Fun,et al. Photoinduced [2+2] cycloadditions (the Paterno–Büchi reaction) of 1-acetylisatin with enol ethers—regioselectivity, diastereoselectivity and acid catalysed transformations of the spirooxetane products , 2002 .
[33] J. Kochi,et al. Oxetanes from [2+2] Cycloaddition of Stilbenes to Quinone via Photoinduced Electron Transfer† , 1999 .
[34] H. Schmickler,et al. Stereoselectivity of Triplet Photocycloadditions:1 Diene−Carbonyl Reactions and Solvent Effects , 1998 .
[35] K. Yoshihara,et al. Picosecond dynamics of excited singlet states in organic microcrystals: Diffuse reflectance laser photolysis study , 1988 .
[36] J. Mattay,et al. Photoreactions of biacetyl with electron-rich olefins: an extended mechanism , 1987 .
[37] F. Fontana,et al. Additions and Corrections - Polar Effects in Free-Radical Reactions. Selectivity and Reversibility in the Homolytic Benzylation of Protonated Heteroaromatic Bases. , 1986 .
[38] C. Ly,et al. Selectivity and Charge Transfer in Photoreactions of α,α,α‐Trifluorotoluene with Olefins , 1986 .
[39] C. Ly,et al. SELECTIVITY AND CHARGE-TRANSFER IN PHOTOREACTIONS OF DONOR-ACCEPTOR SYSTEMS .9. SELECTIVITY AND CHARGE-TRANSFER IN PHOTOREACTIONS OF ALPHA,ALPHA,ALPHA-TRIFLUOROTOLUENE WITH OLEFINS , 1985 .
[40] S. Freilich,et al. Observation of the 1,4 biradical in the Paterno-Buchi reaction , 1981 .
[41] Tai‐Shan Fang,et al. Variable temperature studies on the luminescence from Benzil in a polymethylmethacrylate glass. An example of matrix controlled photorotamerism , 1978 .
[42] M. Charton,et al. Steric effects. I. Esterification and acid-catalyzed hydrolysis of esters , 1975 .
[43] L. Salem. Surface crossings and surface touchings in photochemistry , 1974 .
[44] N. Turro,et al. Molecular photochemistry. L. Molecular photochemistry of alkanones in solution. .alpha.-Cleavage, hydrogen abstraction, cycloaddition, and sensitization reactions , 1972 .
[45] D. Rehm,et al. Kinetics of Fluorescence Quenching by Electron and H‐Atom Transfer , 1970 .
[46] E. S. Lipinsky,et al. Light-catalyzed Organic Reactions. I. The Reaction of Carbonyl Compounds with 2-Methyl-2-butene in the Presence of Ultraviolet Light , 1954 .