Zobrazeno 1 - 10
of 81
pro vyhledávání: '"Jimmie D. Weaver"'
Autor:
Shivangi Kharbanda, Jimmie D. Weaver
Publikováno v:
J Org Chem
Starting with highly fluorinated benzoates, we develop the directed photocatalytic hydrodefluorination (HDF) of fluorinated aryl benzoates and demonstrate its synergistic use with other HDF strategies, along with C–H arylation, decarboxylative coup
Publikováno v:
Chemical Science. 13:9271-9276
In this work, visible light drives a contrathermodynamic isomerization of the classic Stork-Danheiser products through an energy transfer process to yield acyclic distal enone(al) isomers. This is possible because the photochemical energy is transien
Publikováno v:
Organic Letters. 23:1588-1593
Presented is an economical means of removing fluorine from various highly fluorinated arenes using NaBH4. The procedure was adapted for different classes of perfluoroarenes. A novel isomer of an emerging class of organic dyes based on the carbazole p
Autor:
Steven Sittel, Thomas S. Teets, Jimmie D. Weaver, Manjula D. Rathnayake, Jong-Hwa Shon, Dooyoung Kim
Publikováno v:
Chemical Science
Photoredox catalysis has emerged as a powerful strategy in synthetic organic chemistry, but substrates that are difficult to reduce either require complex reaction conditions or are not amenable at all to photoredox transformations. In this work, we
Autor:
Jimmie D. Weaver, Ryne Overfield
Publikováno v:
Springer Handbook of Inorganic Photochemistry ISBN: 9783030637125
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d489adc98126ab2f7d3d408842df8a4d
https://doi.org/10.1007/978-3-030-63713-2_50
https://doi.org/10.1007/978-3-030-63713-2_50
Publikováno v:
Chemical science. 13(32)
Herein, we investigate the use of visible light to indirectly drive ring opening in unstrained 6- and 7-membered ring systems
Publikováno v:
Organic Letters. 21:9681-9687
Net selective bromination and chlorination of activated C-H bonds can be effected in generally high yield via a simple perhalogenation/dehalogenation sequence. The photochemical reductions require no photocatalyst, relying instead on the formation of
Autor:
Justin Briles, Brockton Keen, Jon I. Day, Anuradha Singh, Jimmie D. Weaver, Daniel Jespersen, Duncan Mullins
Publikováno v:
Organic Process Research & Development. 23:1087-1095
Despite the exponential growth of the field of photocatalysis, for reasons that are not entirely clear, these precious photocatalysts are often used in the literature at loadings that exceed their maximum solubility. On an industrial scale, the quant
Publikováno v:
J Org Chem
Within the framework of discovery chemistry, polyfluorination remains a synthetic challenge despite its ability to provide useful characteristics, such as a reduction in the number of hydrogen bond donors and metabolic stability. Coupling a reversal
Publikováno v:
J Fluor Chem
This chemistry establishes a method for the synthesis of per- and poly-fluoroaryl acid amides, utilizing nucleophilic aromatic substitution. Traditionally, such amides are constructed in a two-step process, namely, ammonolysis and then N-acylation. H
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::28cfafc449a61d4ea74d602e112eb3a1
https://europepmc.org/articles/PMC8752095/
https://europepmc.org/articles/PMC8752095/