Zobrazeno 1 - 10
of 60
pro vyhledávání: '"Glenn M. Sammis"'
Autor:
Brodie. J. Thomson, Summer Hanna, Adrian Schwarzenberg, Pirouz Kiani, Dan Bizzotto, Pierre Kennepohl, Ashley Davies, Markus Roggen, Glenn M. Sammis
Publikováno v:
Scientific Reports, Vol 13, Iss 1, Pp 1-9 (2023)
Abstract The legalisation of hemp has led to wide commercial availability of cannabidiol (CBD)-containing products. Here we show that the CBD-hydroxyquinone (HU-331), a readily formed oxidation product and common impurity in CBD isolates, undergoes a
Externí odkaz:
https://doaj.org/article/2a41e22085f94d72a300d5c37586f8c4
Autor:
Tengfei Li, Takahito Kasahara, Jingfu He, Kevan E. Dettelbach, Glenn M. Sammis, Curtis P. Berlinguette
Publikováno v:
Nature Communications, Vol 8, Iss 1, Pp 1-5 (2017)
Photoelectrochemical water splitting is a promising method for H2 fuel production, but the O2 by-product generated has little economic value. Here, Berlinguette and colleagues demonstrate that BiVO4 photoanodes immersed in organic media can instead p
Externí odkaz:
https://doaj.org/article/8c5fd847c07949508ddb948aef2afe21
Publikováno v:
Chemical Science. 14:1775-1780
N-Methylimidazolium sulfinyl fluoride hexafluorophosphate (MISF) was developed as a solution-stable sulfur(iv) reagent to access substituted sulfamate esters using a sulfur(iv) fluoride exchange strategy.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::30d4e5cba9997a470cee226daf3af6f1
https://doi.org/10.1039/d2sc05945b
https://doi.org/10.1039/d2sc05945b
Autor:
Brodie J. Thomson, Samuel R. Khasnavis, Emma C. Grigorian, Rohun Krishnan, Theodore D. Yassa, Kelvin Lee, Glenn M. Sammis, Nicholas D. Ball
Publikováno v:
Chem Commun (Camb)
Herein, we demonstrate two complementary strategies for the syntheses of sulfonyl fluorides using sulfonic acids and their salts. One strategy involves the conversion of sulfonic acid sodium salts to sulfonyl fluorides using thionyl fluoride in 90–
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a3cc8c0c63bd982eb4ff88baf935b759
https://doi.org/10.1039/d2cc05781f
https://doi.org/10.1039/d2cc05781f
Publikováno v:
The Journal of Organic Chemistry. 87:7308-7318
Thionyl fluoride (SOF
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a13fb90c89b6f0d6a18ffb3d7d679678
https://doi.org/10.1021/acs.joc.2c00496
https://doi.org/10.1021/acs.joc.2c00496
Publikováno v:
Chemical Science
Thionyl fluoride (SOF2) was first isolated in 1896, but there have been less than 10 subsequent reports of its use as a reagent for organic synthesis. This is partly due to a lack of facile, lab-scale methods for its generation. Herein we report a no
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2822a904799f89404f4d131b892990e2
https://doi.org/10.1039/d1sc05316g
https://doi.org/10.1039/d1sc05316g
Autor:
Nicholas D. Ball, Nathan C. Friede, Jonathan E. Elisabeth, Alina J. Cook, Glenn M. Sammis, Cayo Lee
Publikováno v:
ACS Catalysis
The past decade has witnessed remarkable growth of catalytic transformations in organic sulfur(VI) fluoride chemistry. This Perspective concentrates exclusively on foundational examples that utilize catalytic strategies to synthesize and react S(VI)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::18872f487293908c6c2cf48a0d737891
https://doi.org/10.1021/acscatal.1c01201
https://doi.org/10.1021/acscatal.1c01201
Autor:
Ryan P. Jansonius, Glenn M. Sammis, Jia Yi Mo, Tengfei Li, David M. Weekes, Curtis P. Berlinguette, Kevan E. Dettelbach
Publikováno v:
ChemSusChem. 13:3622-3626
The photoelectrochemical decomposition of lignin model compounds at a BiVO4 photoanode is demonstrated with simulated sunlight and an applied bias of 2.0 V. These prototypical lignin model compounds are photoelectrochemically converted into the corre
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0673ba6eb51f2529e07be7a7504f7399
https://doi.org/10.1002/cssc.202001134
https://doi.org/10.1002/cssc.202001134
Publikováno v:
Chemistry – A European Journal. 26:4958-4962
The Mitsunobu reaction is a powerful transformation for the one-pot activation and substitution of aliphatic alcohols. Significant efforts have focused on modifying the classic conditions to overcome problems associated with purification from phosphi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::635fa2c7490a95a0ec0fd74c9679bb5b
https://doi.org/10.1002/chem.202000721
https://doi.org/10.1002/chem.202000721
Publikováno v:
Journal of the American Chemical Society. 141:18944-18948
Primary amine products have been prepared using zirconium-catalyzed hydroaminoalkylation of alkenes with N-silylated benzylamine substrates. Catalysis using commercially available Zr(NMe2)4 affords an alternative disconnection to access α-arylated p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a351eb46a8b03b8d163685efc1f87343
https://doi.org/10.1021/jacs.9b10465
https://doi.org/10.1021/jacs.9b10465