Unveiling the impact of the light-source and steric factors on [2+2] heterocycloaddition reactions

[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 .