Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Gary Gallego"'
Autor:
James J. Mousseau, Matthew A. Perry, Mark W. Bundesmann, Gary M. Chinigo, Chulho Choi, Gary Gallego, Robert W. Hicklin, Susan Hoy, David C. Limburg, Neal W. Sach, Yuan Zhang
Publikováno v:
ACS Catalysis. 12:600-606
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4ddd1f32bd550a678ff9e935d0a49144
https://doi.org/10.1021/acscatal.1c05076
https://doi.org/10.1021/acscatal.1c05076
Autor:
Keary Engle, Peng Liu, Indrawan McAlpine, Scott Sutton, Ru Zhou, Ryan Patman, Sajiv Nair, Alexander Burtea, Gary Gallego, Kane Xu, Tuğçe Erbay, Taeho Kang
A unified synthetic strategy to access tertiary four-membered carbo/heterocyclic boronic esters is reported. Use of a Cu(I) catalyst in combination with a modified dppbz ligand enables regioselective hydroboration of various substituted benzylidenecy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b7020d851548d3d912111d42781b9664
https://doi.org/10.26434/chemrxiv.12788390
https://doi.org/10.26434/chemrxiv.12788390
Autor:
Keary Engle, Peng Liu, Indrawan McAlpine, John Braganza, Christopher Ashcroft, Fen Wang, Ryan Patman, Ryan Helsel, Joseph Derosa, Paul Richardson, Michelle Tran-Dubé, Shouliang Yang, Gary Gallego, Huiling Shao, Tuğçe Erbay, Taeho Kang, Jose Medina
The copper-catalyzed hydroboration of benzylidenecyclopropanes, conveniently accessed in one step from readily available benzaldehydes, is reported. Under otherwise identical reaction conditions, two distinct phosphine ligands grant access to differe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::36b8908a497f1419ac5ec7641ae7c518
https://doi.org/10.26434/chemrxiv.8341016
https://doi.org/10.26434/chemrxiv.8341016
Autor:
Jinbao Xiang, Ming Shang, Yu Kawamata, Helena Lundberg, Solomon Reisberg, Miao Chen, Pavel Mykhailiuk, Gregory Beutner, Michael Collins, Alyn Davies, Matthew Del Bel, Gary Gallego, Jillian Spangler, Jeremy T. Starr, Shouliang Yang, Donna Blackmond, Phil Baran
Hindered ethers represent an underexplored area of chemical space due to the difficulty and inoperability associated with conventional reactions, despite the high-value of such structural motifs in a variety of societal applications. Demonstrated her
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5ffbc16c64c698859d534d7ba2285def
https://doi.org/10.26434/chemrxiv.8144294
https://doi.org/10.26434/chemrxiv.8144294
Autor:
Rei Matsuura, Tanner Jankins, Kin Yang, Gary Gallego, Shouliang Yang, Mingying He, Fen Wang, Rohan Marsters, Indrawan McAlpine, Keary Engle
A catalytic γ-selective syn-hydroarylation of alkenyl carbonyl compounds using arylboronic acids has been developed using a substrate directivity approach with a palladium(II) catalyst. This method tolerates a wide range of functionalized (hetero)ar
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::db59ccbc5881317653c9a8da950ac4b4
https://doi.org/10.26434/chemrxiv.6148124
https://doi.org/10.26434/chemrxiv.6148124
Autor:
Christopher J. T. Hyland, Leera Choi, Yi-Hsun Chen, Fu-Ming Tao, Alireza Ariafard, David Sandoval, Brian F. Yates, Gary Gallego, Kiet Tran
Publikováno v:
ChemInform. 42
TiCl4 and TiBr4 rapidly transform cyclopropenylmethyl acetates to (E)-halodienes via ring-opening to allyl-vinyl cations. DFT calculations suggest that the regioselectivity of the halogenation of this cationic intermediate by [TiX4OAc]− is under th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::881c2b344823b04b240e1bbc35dad6ce
https://doi.org/10.1002/chin.201134061
https://doi.org/10.1002/chin.201134061
Autor:
Leera Choi, Gary Gallego, David Sandoval, Christopher J. T. Hyland, Yi-Hsun Chen, Alireza Ariafard, Fu-Ming Tao, Brian F. Yates, Kiet Tran
Publikováno v:
Organic & Biomolecular Chemistry. 9:3359
TiCl(4) and TiBr(4) rapidly transform cyclopropenylmethyl acetates to (E)-halodienes via ring-opening to allyl-vinyl cations. DFT calculations suggest that the regioselectivity of the halogenation of this cationic intermediate by [TiX(4)OAc](-) is un
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::45c971583b277be150a06bb00e8a1cdb
https://doi.org/10.1039/c0ob01046d
https://doi.org/10.1039/c0ob01046d