Ruthenium‐Catalyzed Double C(sp 2 )−H Functionalizations of Fumaramides with Alkynes for the Divergent Synthesis of Pyridones and Naphthyridinediones

Autor: Bao-Xiu Tao, Zhi-Hong Du, Yumin Li, Zuoyi Jiao, Zhijian Han, Chao-Shan Da, Ze‐Xuan Zhang, Wei‐Ping Li, Hao Chen

Publikováno v: ChemCatChem. 12:2538-2547

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::2da17205938d930808ab4221c752ba85
https://doi.org/10.1002/cctc.201902160

Thermally and Photochemically Induced Dethreading of Fumaramide-Based Kinetically Stable Pseudo[2]rotaxanes

Autor: Fatima Morales, Juan Carlos Martinez-Costa, Grace R. Marley, Delia Bautista, Adrian Lopez-Lopez, Jose Berna, Alberto Martinez-Cuezva, Mateo Alajarin

Publikováno v: European Journal of Organic Chemistry. 2019:3480-3488

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::1f41942cb0e280070b84170b43a47d73
https://doi.org/10.1002/ejoc.201900073

Helical Foldamers Incorporating Photoswitchable Residues for Light-Mediated Modulation of Conformational Preference

Autor: Marco Crisma, Alessandro Moretto, Jonathan Clayden, Giulia Marafon, Matteo De Poli, Cristina Peggion, Daniela Mazzier

Publikováno v: Mazzier, D, Crisma, M, De Poli, M, Marafon, G, Peggion, C, Clayden, J & Moretto, A 2016, ' Helical foldamers incorporating photoswitchable residues for light-mediated modulation of conformational preference ', Journal of the American Chemical Society, vol. 138, no. 25, pp. 8007-8018 . https://doi.org/10.1021/jacs.6b04435
Journal of the American Chemical Society
138 (2016): 8007–8018. doi:10.1021/jacs.6b04435
info:cnr-pdr/source/autori:Mazzier, Daniela; Crisma, Marco; De Poli, Matteo; Marafon, Giulia; Peggion, Cristina; Clayden, Jonathan; Moretto, Alessandro/titolo:Helical Foldamers Incorporating Photoswitchable Residues for Light-Mediated Modulation of Conformational Preference/doi:10.1021%2Fjacs.6b04435/rivista:Journal of the American Chemical Society (Print)/anno:2016/pagina_da:8007/pagina_a:8018/intervallo_pagine:8007–8018/volume:138

An E unsaturated fumaramide linkage may be introduced into Aib peptide foldamer structures by standard coupling methods and photoisomerized to its Z (maleamide) isomer by irradiation with UV light. As a result of the photoisomerization, a new hydroge

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::206a3e84a01522a1b4f9cc26c16026f8
https://doi.org/10.1021/jacs.6b04435

Photoswitchable interlocked thiodiglycolamide as a cocatalyst of a chalcogeno-Baylis-Hillman reaction

Autor: Alberto Martinez-Cuezva, Jose Berna, Tomas Nicolas-Garcia, Mateo Alajarin, Cristian Navarro, Adrian Saura-Sanmartin, Raul-Angel Orenes

Publikováno v: Chemical Science

The sulfur-based template of light-driven molecular shuttles is able to modulate its catalytic activity in a diastereoselective chalcogeno-Baylis–Hillman reaction.
En route to a photoswitchable interlocked catalyst we have proved the ability o

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8d233b7dc888997eebf95b34850399c8
https://pubmed.ncbi.nlm.nih.gov/28580109

Asymmetric synthesis of 2-substituted butane-1,4-diols by hydrogenation of homochiral fumaramide derivatives

Autor: Samaila Jawaid, Louis J. Farrugia, David J. Robins

Publikováno v: Tetrahedron: Asymmetry. 15:3979-3988

Diastereoselective hydrogenation of homochiral fumaramides 1 derived from (2R)-Oppolzer’s sultam was observed by analysis of the 1H NMR spectra of the succinamide mixtures with de’s of 77–88%. Reduction of these succinamides using LiAlH4 gave t

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::7593e1431c18a41ae3e769104127cbc6
https://doi.org/10.1016/j.tetasy.2004.11.023