Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Lucille A. Wells"'
Autor:
Cong Wang, Hui Zhang, Lucille A. Wells, Tian Liu, Tingting Meng, Qingchao Liu, Patrick J. Walsh, Marisa C. Kozlowski, Tiezheng Jia
Publikováno v:
Nature Communications, Vol 12, Iss 1, Pp 1-11 (2021)
N-Arylation of NH-diaryl sulfoximines faces synthetic challenges among reported methods. Here, the authors present a mild copper-catalyzed photoredox dehydrogenative Chan-Lam coupling of free diaryl sulfoximines and arylboronic acids via an auto-cata
Externí odkaz:
https://doaj.org/article/b3b7c585ed974409961529e6bcd67547
Autor:
Léa Thai-Savard, Morgane Sayes, Josiane Perreault-Dufour, Gang Hong, Lucille A. Wells, Marisa C. Kozlowski, André B. Charette
Publikováno v:
The Journal of Organic Chemistry. 88:1515-1521
Autor:
Tingting Meng, Lucille A. Wells, Tianxin Wang, Jinyu Wang, Shishuo Zhang, Jie Wang, Marisa C. Kozlowski, Tiezheng Jia
Publikováno v:
Journal of the American Chemical Society. 144:12476-12487
Inspired by the discovery of a S═N bond in the collagen IV network and its essential role in stabilizing basement membranes, sulfilimines have drawn much attention in the fields of chemistry and biology. However, their further uptake is hindered by
Autor:
Lucille A. Wells, Michael R. Gau, Michael B. Peddicord, Kirsten F. Bostwick, Marisa C. Kozlowski, Michael J. Zacuto
Publikováno v:
Organic Process Research & Development. 26:1803-1811
Autor:
kaiming han, shufeng chen, Tiezheng Jia, qingjin liang, Lucille A. Wells, Marisa C. Kozlowski
Herein, an unprecedented synthetic route to sulfilimines via a copper-catalyzed Chan-Lam-type coupling of sulfenamides is presented. A key to success in this novel transformation is the chemoselective S-arylation of S(II) sulfenamides to form the S(I
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::13b2879fab986b2a09168e66e83da522
https://doi.org/10.21203/rs.3.rs-1037799/v1
https://doi.org/10.21203/rs.3.rs-1037799/v1
Autor:
Edward F. C. Byrd, Jesse J. Sabatini, Joshua A. Orlicki, Lucille A. Wells, Joseph E Banning, Rosario C. Sausa, Eric C. Johnson, David E. Chavez
Publikováno v:
ChemPlusChem. 85:237-239
The synthesis and crystal structure of the heterocyclic explosive bis(nitroxymethylisoxazolyl) furoxan, C10 H6 N6 O10 , are described. In addition, we report its physical properties and theoretical performance. This material was found to exhibit stan
Autor:
Linglin Wu, Lucille A. Wells, Bo Qu, Olga V. Zatolochnaya, Jinhua J. Song, Yongda Zhang, Marisa C. Kozlowski, Ling Wu, Chris H. Senanayake
Publikováno v:
Organic Letters. 21:8952-8956
A Cu-catalyzed enantioselective aminoboration of E-vinylarenes with pivZPhos as a ligand is reported. Enantioenriched aminoborates are prepared with excellent regio- and enantioselectivities up to >99:1 er under the optimized conditions. The utility
Autor:
Qingchao Liu, Lucille A. Wells, Patrick J. Walsh, Tian Liu, Tingting Meng, Cong Wang, Hui Zhang, Tiezheng Jia, Marisa C. Kozlowski
Publikováno v:
Nature Communications
Nature Communications, Vol 12, Iss 1, Pp 1-11 (2021)
Nature Communications, Vol 12, Iss 1, Pp 1-11 (2021)
N-Arylation of NH-sulfoximines represents an appealing approach to access N-aryl sulfoximines, but has not been successfully applied to NH-diaryl sulfoximines. Herein, a copper-catalyzed photoredox dehydrogenative Chan-Lam coupling of free diaryl sul
Publikováno v:
Chemical communications (Cambridge, England). 55(17)
Polycyclic N-oxides were developed based on the heterocycles 1,2,4,5-tetrazine and 4H,8H-difurazano[3,4-b:3′,4′-e]pyrazine. The new compounds are energetic and have excellent explosive properties, while maintaining low mechanical sensitivities. M