Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Victoria Dimakos"'
A Morita–Baylis–Hillman Inspired Cross-Coupling Strategy for the Direct α-Arylation of Cyclic Enones
Autor:
Victoria Dimakos, Daniel P. Canterbury, Sebastien Monfette, Philipp C. Roosen, Stephen G. Newman
Publikováno v:
ACS Catalysis. 12:11557-11562
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::01a81f8ef01d5e7e3fc06e26cddd31fb
https://doi.org/10.1021/acscatal.2c03448
https://doi.org/10.1021/acscatal.2c03448
Autor:
Victoria Dimakos, Stephen G. Newman
Publikováno v:
The Power of High-Throughput Experimentation: Case Studies from Drug Discovery, Drug Development, and Catalyst Discovery (Volume 2) ISBN: 9780841297555
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b22604c7cc2a1440ec5cbae4624575cd
https://doi.org/10.1021/bk-2022-1420.ch009
https://doi.org/10.1021/bk-2022-1420.ch009
Autor:
Victoria Dimakos, Stephen G. Newman
Publikováno v:
Chem Catalysis. 1:1354-1356
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f19f21beb05e8b95121bd3c778514fc4
https://doi.org/10.1016/j.checat.2021.11.008
https://doi.org/10.1016/j.checat.2021.11.008
Publikováno v:
Chemical Communications. 57:12135-12138
Site-selective oxidations of carbohydrates, employing acridinium photocatalysis and quinuclidine hydrogen atom transfer catalysis, are presented. Protocols have been developed for oxidations of all-equatorial carbohydrates as well as those containing
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::31c49ae8ec9005f0c8e9ec7af98ad784
https://doi.org/10.1039/d1cc05124e
https://doi.org/10.1039/d1cc05124e
Autor:
Victoria Dimakos, Mark S. Taylor
Publikováno v:
Organic & Biomolecular Chemistry. 19:514-524
Methods for the O-arylation of hydroxyl and hemiacetal groups in carbohydrates via C(sp2)-O bond formation are discussed. Such methods provide an alternative disconnection to the traditional approach of nucleophilic substitution between a sugar-deriv
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5933aeef4d1de92f70ef9adc44bd37e3
https://doi.org/10.1039/d0ob02009e
https://doi.org/10.1039/d0ob02009e
Publikováno v:
Organic & Biomolecular Chemistry. 17:5671-5674
Copper-mediated couplings of arylboroxines with glycosyl hemiacetals furnish O-aryl glycosides via Csp2-O bond formation. The method enables the anomeric O-arylation of protected pyranose and furanose derivatives, and is tolerant of functionalized ar
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::13c73dca3ba2c749a70ce97521808b1e
https://doi.org/10.1039/c9ob01022j
https://doi.org/10.1039/c9ob01022j
Autor:
Victoria Dimakos, Mark S. Taylor
Publikováno v:
Chemical Reviews. 118:11457-11517
Methods for site-selective transformations of hydroxyl groups in carbohydrate derivatives are reviewed. The construction of oligosaccharides of defined connectivity hinges on such transformations, which are also needed for the preparation of modified
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d575aba5e711dd63877e39666ea5cb9e
https://doi.org/10.1021/acs.chemrev.8b00442
https://doi.org/10.1021/acs.chemrev.8b00442
Autor:
Victoria, Dimakos, Mark S, Taylor
Publikováno v:
Organicbiomolecular chemistry. 19(3)
Methods for the O-arylation of hydroxyl and hemiacetal groups in carbohydrates via C(sp2)-O bond formation are discussed. Such methods provide an alternative disconnection to the traditional approach of nucleophilic substitution between a sugar-deriv
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::0f558259e16d6668bd1076c2cebad272
https://pubmed.ncbi.nlm.nih.gov/33331387
https://pubmed.ncbi.nlm.nih.gov/33331387
Autor:
Marion H. Emmert, Matthieu Jouffroy, David C. Leitch, Alexander Buitrago Santanilla, Gemma Cook, Amanda Dombrowski, Nathan Gesmundo, Dipannita Kalyani, Mycah Uehling, Michael Wleklinski, Nicole C. Goodwin, Katherine Honicker, Jonathan Latham, Katherine M. P. Wheelhouse, Sabine Fenner, Matthew P. Whiting, Chunrui Sun, Ji Qi, Feng Peng, Niki R. Patel, Danielle Schultz, Orion Staples, Jacob S. Mohar, Daniel J. Mindiola, Victoria Dimakos, Stephen G. Newman, Stig D. Friis, Erik Weis, Magnus J. Johansson
'High-throughput experimentation (HTE) is an emerging and powerful approach to problems in organic chemistry and homogeneous catalysis. This book is targeted at both experts and those new to the field who are seeking general perspectives and design p
Publikováno v:
Journal of the American Chemical Society. 139:15515-15521
Site-selective functionalization of hydroxy groups in sugar derivatives is a major challenge in carbohydrate synthesis. Methods for achieving this goal will provide efficient access to new sugar-derived chemical building blocks and will facilitate th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f992e3a5cda6def6c5b0bb7238017b05
https://doi.org/10.1021/jacs.7b09420
https://doi.org/10.1021/jacs.7b09420