Literatura académica sobre el tema "Enone Transposition"
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Artículos de revistas sobre el tema "Enone Transposition"
Kutney, James P. y Carles Cirera. "The chemistry of thujone. XX. New enantioselective syntheses of Ambrox and epi-Ambrox". Canadian Journal of Chemistry 75, n.º 8 (1 de agosto de 1997): 1136–50. http://dx.doi.org/10.1139/v97-136.
Texto completoCollins, Jonathan A., Christopher J. Gerry y Madeleine M. Duncan. "A Chemoenzymatic Formal Synthesis of Epoxyquinols A and B". Synlett 30, n.º 19 (23 de octubre de 2019): 2193–97. http://dx.doi.org/10.1055/s-0039-1690216.
Texto completoMa, Xinghua, Xin Liu, Patrick Yates, Warwick Raverty, Martin G. Banwell, Chenxi Ma, Anthony C. Willis y Paul D. Carr. "Manipulating the enone moiety of levoglucosenone: 1,3-Transposition reactions including ones leading to isolevoglucosenone". Tetrahedron 74, n.º 38 (septiembre de 2018): 5000–5011. http://dx.doi.org/10.1016/j.tet.2018.03.023.
Texto completoHantos, Susanne M., Sasmita Tripathy, Najma Alibhai y Tony Durst. "Synthesis of trichiliasterones A and B 16-Ketosteroids isolated from Trichilia hirta and Trichilia americana". Canadian Journal of Chemistry 79, n.º 11 (1 de noviembre de 2001): 1747–53. http://dx.doi.org/10.1139/v01-126.
Texto completoAthawale, Paresh R., Vishal M. Zade, Gamidi Rama Krishna y D. Srinivasa Reddy. "Tuning of α-Silyl Carbocation Reactivity into Enone Transposition: Application to the Synthesis of Peribysin D, E-Volkendousin, and E-Guggulsterone". Organic Letters 23, n.º 17 (13 de agosto de 2021): 6642–47. http://dx.doi.org/10.1021/acs.orglett.1c02173.
Texto completoHudlicky, Jason R., Lukas Werner, Vladislav Semak, Razvan Simionescu y Tomas Hudlicky. "Dauben–Michno oxidative transposition of allylic cyanohydrins — Enantiomeric switch of (–)-carvone to (+)-carvone*Based on the 2010 Bader Award Lecture." Canadian Journal of Chemistry 89, n.º 5 (mayo de 2011): 535–43. http://dx.doi.org/10.1139/v11-026.
Texto completoBaptistella, Lúcia H. B. y Adriana M. Aleixo. "α′-HYDROXY-α,β-UNSATURATED TOSYLHYDRAZONES: PREPARATION AND USE AS INTERMEDIATES FOR CARBONYL AND ENONE TRANSPOSITIONS". Synthetic Communications 32, n.º 19 (enero de 2002): 2937–50. http://dx.doi.org/10.1081/scc-120012982.
Texto completoNagasawa, Shota, Yusuke Sasano y Yoshiharu Iwabuchi. "Catalytic Oxygenative Allylic Transposition of Alkenes into Enones with an Azaadamantane‐Type Oxoammonium Salt Catalyst". Chemistry – A European Journal 23, n.º 43 (12 de julio de 2017): 10276–79. http://dx.doi.org/10.1002/chem.201702512.
Texto completoBaptistella, Lucia H. B. y Adriana M. Aleixo. "α′-Hydroxy-α,β-unsaturated Tosylhydrazones: Preparation and Use as Intermediates for Carbonyl and Enone Transpositions." ChemInform 34, n.º 2 (14 de enero de 2003). http://dx.doi.org/10.1002/chin.200302152.
Texto completoTesis sobre el tema "Enone Transposition"
Otoo, Barnabas. "Conjugate Additions and Transposition of the Allylic Alcohols of Enol Ethers of 1, 2-Cyclohexanedione". Digital Commons @ East Tennessee State University, 2010. https://dc.etsu.edu/etd/1748.
Texto completoCampolo, Damien. "Transfert de chiralité dans les réarrangements en cascade d'ènediynes". Thesis, Aix-Marseille, 2013. http://www.theses.fr/2013AIXM4339/document.
Texto completoThe asymmetric synthesis of azaheterocycles (tetrahydorisoquinolines and naphthodiazepines) was successfully achieved via the polar/radical cross-over rearrangement of enediynes bearing a stereogenic center. This process involves successively : enyne-allene formation (via 1,3-proton shift, reaction of a terminal alkyne group with carbenoids or Crabbé homologation)/Saito-Myers cyclization/1,5-hydrogen atom transfer/biradical recombination. It was ideally suited to apply a strategy based on the memory of chirality phenomenon. Mechanistic studies based on isotopic labelling and theoretical calculations enabled to go deeper into the understanding of the parameters controlling the regio- and the stereoselectivity of the reaction. The ambition to control two stereogenic centers via double memory of chirality, led us to investigate the transfer of the axial chirality of a designed allenic moiety. This study led to the discovery of an original copper (I)-mediated cycloisomerization leading to chiral fulvenes and proceeding via central-to-axial-to-central double chirality transfer
Capítulos de libros sobre el tema "Enone Transposition"
Taber, Douglass F. "The Tanino/Miyashita Synthesis of Solanoeclepin A". En Organic Synthesis. Oxford University Press, 2013. http://dx.doi.org/10.1093/oso/9780199965724.003.0104.
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