Zobrazeno 1 - 10
of 105
pro vyhledávání: '"Dale F, Shellhamer"'
Autor:
Dale F. Shellhamer, Zachary J. Beavis, Dakota L. Brady, Marcela S. Bucardo, Sarah L. Elwin, Nicholas Fiorella, Leticia Gomez, Sara Van Horne, Marc C. Perry
Publikováno v:
Results in Chemistry, Vol 2, Iss , Pp 100015- (2020)
Line-broadening by NMR is an easy and fast method to detect radical intermediates in solution. Chlorosulfonyl isocyanate reacts with electron-rich alkenes via a Single Electron Transfer pathway to give 1,4-diradical intermediates. The Triplet 1,4-dir
Externí odkaz:
https://doaj.org/article/7e3013ea33ab4c979dfdbc0dbcb37dd4
Publikováno v:
Journal of Agricultural and Food Chemistry. 69:2069-2075
Acrolein hydrolysis byproducts are a part of good industrial stewardship practice. Aqueous acrolein is used worldwide as an industrial raw material, an herbicide, an oilfield biocide, a hydrogen sulfide scavenger, and a molluscicide. Industrial acrol
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::53f61c577c6f6bb2decd12e6d5f6afad
https://doi.org/10.1021/acs.jafc.0c07339
https://doi.org/10.1021/acs.jafc.0c07339
Publikováno v:
Journal of agricultural and food chemistry. 69(7)
Acrolein hydrolysis byproducts are a part of good industrial stewardship practice. Aqueous acrolein is used worldwide as an industrial raw material, an herbicide, an oilfield biocide, a hydrogen sulfide scavenger, and a molluscicide. Industrial acrol
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::9f6682c057116eaa1746701575230d8e
https://pubmed.ncbi.nlm.nih.gov/33565881
https://pubmed.ncbi.nlm.nih.gov/33565881
Autor:
Dakota L. Brady, Sara Van Horne, Marc C. Perry, Leticia Gomez, Nicholas Fiorella, Marcela S. Bucardo, Sarah L. Elwin, Dale F. Shellhamer, Zachary J. Beavis
Publikováno v:
Results in Chemistry, Vol 2, Iss, Pp 100015-(2020)
Line-broadening by NMR is an easy and fast method to detect radical intermediates in solution. Chlorosulfonyl isocyanate reacts with electron-rich alkenes via a Single Electron Transfer pathway to give 1,4-diradical intermediates. The Triplet 1,4-dir
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0b394e3e160bc503dd26f0bc9d4b3079
http://www.sciencedirect.com/science/article/pii/S2211715619300153
http://www.sciencedirect.com/science/article/pii/S2211715619300153
Autor:
Ryan D. Robinson, Jacob C. Milligan, Lincoln B. Smith, Christine J. Licata, Dale F. Shellhamer, Summer A. Bunting, Kelsey L. Alexander, Marc C. Perry, Danielle E. Shipowick, Sarah L. Elwin
Publikováno v:
Synthesis. 47:1944-1950
Chlorosulfonyl isocyanate (CSI) is a sluggish electrophile in reactions with electron-deficient alkenes or with many monofluoroalkenes. The efficiency of these reactions is improved at temperatures between –15 and 25 °C because, at these temperatu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d807129f3270656ef4aa2e295bf94225
https://doi.org/10.1055/s-0034-1380553
https://doi.org/10.1055/s-0034-1380553
Autor:
Danielle E. Shipowick, Summer A. Bunting, Jacob C. Milligan, Parker C Horn, Marc C. Perry, Jerry A. Boatz, David J Vandenbroek, Dale F. Shellhamer, Kelli R Hickle, Lincoln B. Smith
Publikováno v:
The Journal of Organic Chemistry. 78:246-252
Chlorosulfonyl isocyanate (CSI) is reported to react with hydrocarbon alkenes by a stepwise dipolar pathway to give N-chlorosulfonyl-β-lactams that are readily reduced to β-lactams. Substitution of a vinyl hydrogen for a vinyl fluorine changes the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::62c798d5ee1a64822d69e8c5dc6825c5
https://doi.org/10.1021/jo3016488
https://doi.org/10.1021/jo3016488
Autor:
Ryan H. DeBoard, Dennis C. Madrid, Torie L. Hartge, Dale F. Shellhamer, Peter E. Baker, Jeffrey L. Boerneke, Geoffrey A. Sigmund, Victor L. Heasley, Ashley M. Ramirez
Publikováno v:
Letters in Organic Chemistry. 4:500-504
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8c810fe5d16fc499be1442fbbe449709
https://doi.org/10.2174/157017807782006317
https://doi.org/10.2174/157017807782006317
Autor:
Dale F. Shellhamer, Ryan D. Robinson, Danielle E. Shipowick, Christine J. Licata, Jacob C. Milligan, Summer A. Bunting, Marc C. Perry, Lincoln B. Smith, Sarah L. Elwin, Kelsey L. Alexander
Publikováno v:
ChemInform. 46
The equilibrium between two separate reactants and a complex or SET intermediate formed by them shifts towards the unimolecular intermediate between -15 and 25°, therefore, the efficiency of the electrophile (II) is improved under the reaction condi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a02d9dfed246e2b8600759998be52865
https://doi.org/10.1002/chin.201550111
https://doi.org/10.1002/chin.201550111
Publikováno v:
Journal of Fluorine Chemistry. 124:17-20
Ionic chlorination of 1H,1H,7H-perfluorohept-1-ene (2) and heptafluoropropyl trifluorovinyl ether (4) with chlorine monofluoride (ClF) gas in aprotic solvent; and alkenes 2, 1H-perfluorohept-1-ene (3E), and 4 with chlorine (Cl2) in protic solvent wer
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::52d97230b65349e7376388fc26937249
https://doi.org/10.1016/s0022-1139(03)00169-6
https://doi.org/10.1016/s0022-1139(03)00169-6
Autor:
Dale F. Shellhamer, Victor L. Heasley, Andrew J. Ryan, David C. Gleason, Jeffrey J Lehman, G.Gawayne Vaughan, Peter K Titterington
Publikováno v:
Journal of Fluorine Chemistry. 123:171-176
Ionic and photochemical reaction of chlorine (Cl2), bromine (Br2) and iodine monochloride (ICl) to hexafluoro-1,3-butadiene (1) and 1,3-butadiene (2) were carried out under conditions that would provide product distributions under controlled ionic or
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bc17bb8eec62bc51089d320c3df2f532
https://doi.org/10.1016/s0022-1139(03)00115-5
https://doi.org/10.1016/s0022-1139(03)00115-5