Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Nicholas C. Pflug"'
Autor:
Rameez Ali, Sreenivasa Anugu, Reena Chawla, Violeta G. Demillo, Florian Goulinet-Mateo, Sagar Gyawali, Sunil Hamal, Dylan E. Jones, Katrin Lamprecht, Truc Le, Liezel A. Lumangtad, Nicholas C. Pflug, Alekhya Sama, Emily D. Scarbrough, Thomas W. Bell
Publikováno v:
ACS Omega, Vol 4, Iss 1, Pp 1254-1264 (2019)
Externí odkaz:
https://doaj.org/article/011f439bb7a647cc920377bf1d077276
Autor:
Matthew Grobstein, Christopher J Knutson, David M. Cwiertny, Nicholas C. Pflug, Wyanna Yeung, James B. Gloer, Eric V. Patterson
Publikováno v:
Environmental Science & Technology
Environmental Science & Technology, 55 (21)
Environmental Science & Technology, 55 (21)
There is growing interest in the fate and effects of transformation products generated from emerging pollutant classes, and new tools that help predict the products most likely to form will aid in risk assessment. Here, using a family of structurally
Autor:
Edward P. Kolodziej, Andrew K Kral, James B. Gloer, David M. Cwiertny, Kristine H. Wammer, Kathryn C Breuckman, Madeline K. Hankard, Nicholas C. Pflug
Publikováno v:
Environmental Science & Technology. 54:12181-12190
Photolysis of trenbolone acetate (TBA) metabolites in the presence of various nitrogen-, sulfur-, or oxygen-containing nucleophiles (e.g., azide, ammonia, or thiosulfate, respectively) results in r...
Autor:
Kristine H. Wammer, Kristopher McNeill, David M. Cwiertny, Edward P. Kolodziej, Dalma Martinović-Weigelt, James B. Gloer, Nicholas C. Pflug, Eric V. Patterson
Publikováno v:
The Journal of Organic Chemistry. 84:11366-11371
While studying the environmental fate of potent endocrine-active steroid hormones, we observed the formation of an intramolecular [2 + 2] photocycloaddition product (2) with a novel hexacyclic ring system following the photolysis of altrenogest (1).
Autor:
Nicholas C. Pflug, Andrew E. Kral, David M. Cwiertny, John D. Sivey, Monica E. McFadden, Gregory H. LeFevre
Publikováno v:
Environmental Science & Technology. 53:6738-6746
Dichloroacetamide safeners are commonly added to commercial chloroacetamide herbicide formulations and widely used worldwide, but their environmental fate has garnered little scrutiny as a result of their classification as "inert" ingredients. Here,
Autor:
James B. Gloer, Kristine H. Wammer, Dalma Martinović-Weigelt, Christopher J Knutson, Dale C. Swenson, David M. Cwiertny, Nicholas C. Pflug
Publikováno v:
Organic Letters. 21:3568-3571
In an ongoing effort to study the environmental fate of endocrine-active steroid hormones, we report the formation of phenolic rearrangement products (3 and 4) with a novel 6,5,8,5-ring system following aqueous photolysis of dienogest (1) and methyld
Publikováno v:
Journal of Materials Chemistry A, 9 (10)
The electrochemical valorization of glycerol, a by-product from biodiesel production, has received significant attention, yet systems for the efficient reforming of glycerol that are based on non-precious metals have rarely been reported. Here, we in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e6511971efaf655e4a4134b105c69671
Autor:
Nicholas C. Pflug, Eden M. DeWald, Dana W. Kolpin, David M. Cwiertny, Gregory H. LeFevre, Michelle L. Hladik, Kathryn L. Klarich
Publikováno v:
Environmental Science & Technology Letters. 4:168-173
Neonicotinoid insecticides are widespread in surface waters across the agriculturally intensive Midwestern United States. We report for the first time the presence of three neonicotinoids in finished drinking water and demonstrate their general persi
Publikováno v:
Environmental sciencetechnology. 53(19)
Fludioxonil is a pyrrole-containing pesticide whose registration as a plant protection product is currently under review in the United States and Europe. There are concerns over its potential persistence and toxicity in the aquatic environment; howev
Autor:
Thomas W. Bell, Nicholas C. Pflug, Sreenivasa Anugu, Florian Goulinet-Mateo, Katrin Lamprecht, Reena Chawla, Rameez Ali, Violeta G. Demillo, Emily D. Scarbrough, Sunil Hamal, Alekhya Sama, Sagar Gyawali, Truc D. T. Le, Liezel A. Lumangtad, Dylan E. Jones
Publikováno v:
ACS Omega, 4 (1)
ACS Omega, Vol 4, Iss 1, Pp 1254-1264 (2019)
ACS Omega
ACS Omega, Vol 4, Iss 1, Pp 1254-1264 (2019)
ACS Omega
Macrocyclic triamine disulfonamides can be synthesized by double Tsuji–Trost N-allylation reaction of open-chain disulfonamides with 2-alkylidene-1,3-propanediyl bis(carbonates). The previously used Atkins–Richman macrocyclization method generall
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::168293d30a812016f387b7d87a176d1c
https://hdl.handle.net/20.500.11850/322310
https://hdl.handle.net/20.500.11850/322310