Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Zane G. Long"'
Autor:
Zane G. Long, Jonathan V. Le, Benjamin B. Katz, Belen G. Lopez, Emily D. Tenenbaum, Bonnie Semmling, Ryan J. Schmidt, Felix Grün, Carter T. Butts, Rachel W. Martin
Publikováno v:
Applications in Plant Sciences, Vol 11, Iss 5, Pp n/a-n/a (2023)
Abstract Premise Matrix‐assisted laser desorption/ionization mass spectrometry imaging (MALDI‐MSI) is a chemical imaging method that can visualize spatial distributions of particular molecules. Plant tissue imaging has so far mostly used cryosect
Externí odkaz:
https://doaj.org/article/3e0423e1ee694ce29f2b666ec2c514fb
Autor:
Barry E. Rich, Jayme C. Jackson, Lizett Ortiz de Ora, Zane G. Long, Kylie S. Uyeda, Elizabeth N. Bess
Publikováno v:
Journal of applied microbiology, vol 133, iss 3
Aims The gut microbiota modulates dopamine levels in vivo, but the bacteria and biochemical processes responsible remain incompletely characterized. A potential precursor of bacterial dopamine production is 3-methoxytyramine (3MT); 3MT is produced wh
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f8ed6c1767bfa9b801193889d40f5f87
https://doi.org/10.1111/jam.15682
https://doi.org/10.1111/jam.15682
Autor:
Sean S Nguyen, Jennifer A. Prescher, Robert S Dorn, R. David Row, Zane G Long, Tyler K. Heiss, Andrew J. Ferreira
Publikováno v:
Org Lett
Organic letters, vol 21, iss 21
Organic letters, vol 21, iss 21
A general method to synthesize substituted butenolides from hydroxymethylcyclopropenones is reported. Functionalized cyclopropenones undergo ring-opening reactions with catalytic amounts of phosphine, forming reactive ketene ylides. These intermediat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1b6f7dfdeed9e63fa1449b8a703bff52
https://pubmed.ncbi.nlm.nih.gov/31622107
https://pubmed.ncbi.nlm.nih.gov/31622107
Autor:
David N Kamber, Jeffrey S Briggs, Sean S Nguyen, R. David Row, Hui-Wen Shih, Zane G Long, Fang Liu, K. N. Houk, Jennifer A. Prescher, Yong Liang
Publikováno v:
Chemical Science
Isomeric triazines can be tuned to exhibit unique reaction profiles with biocompatible strained alkenes and alkynes.
Expanding the scope of bioorthogonal reactivity requires access to new and mutually compatible reagents. We report here that 1,2
Expanding the scope of bioorthogonal reactivity requires access to new and mutually compatible reagents. We report here that 1,2
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::11b55943f3cb08d1015e95c9a481cb3f
https://pubmed.ncbi.nlm.nih.gov/31908754
https://pubmed.ncbi.nlm.nih.gov/31908754