Zobrazeno 1 - 10
of 22
pro vyhledávání: '"Douglas Mans"'
Autor:
Bin Hu, Shane Canon, Emiley A. Eloe-Fadrosh, Anubhav, Michal Babinski, Yuri Corilo, Karen Davenport, William D. Duncan, Kjiersten Fagnan, Mark Flynn, Brian Foster, David Hays, Marcel Huntemann, Elais K. Player Jackson, Julia Kelliher, Po-E. Li, Chien-Chi Lo, Douglas Mans, Lee Ann McCue, Nigel Mouncey, Christopher J. Mungall, Paul D. Piehowski, Samuel O. Purvine, Montana Smith, Neha Jacob Varghese, Donald Winston, Yan Xu, Patrick S. G. Chain
Publikováno v:
Frontiers in Bioinformatics, Vol 1 (2022)
The nascent field of microbiome science is transitioning from a descriptive approach of cataloging taxa and functions present in an environment to applying multi-omics methods to investigate microbiome dynamics and function. A large number of new too
Externí odkaz:
https://doaj.org/article/dc6956a6b3c54bc0a65af4d854b974d9
Autor:
Maggie M. Bowman, Alexis E. Heath, Tamas Varga, Anil K. Battu, Rosalie K. Chu, Jason Toyoda, Tanya E. Cheeke, Stephanie S. Porter, Kevan Moffett, Brittany Letendre, Odeta Qafoku, John R. Bargar, Douglas Mans, Nancy Hess, Emily B. Graham
Publikováno v:
Frontiers in Soil Science. 3
While significant progress has been made in understanding global carbon (C) cycling, the mechanisms regulating belowground C fluxes and storage are still uncertain. New molecular technologies have the power to elucidate these processes, yet we have n
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::38b97220bd76dde7bfedcb3a87518b4e
Autor:
Bin Hu, Shane Canon, Emiley A. Eloe-Fadrosh, null Anubhav, Michal Babinski, Yuri Corilo, Karen Davenport, William D. Duncan, Kjiersten Fagnan, Mark Flynn, Brian Foster, David Hays, Marcel Huntemann, Elais K. Player Jackson, Julia Kelliher, Po-E. Li, Chien-Chi Lo, Douglas Mans, Lee Ann McCue, Nigel Mouncey, Christopher J. Mungall, Paul D. Piehowski, Samuel O. Purvine, Montana Smith, Neha Jacob Varghese, Donald Winston, Yan Xu, Patrick S. G. Chain
Publikováno v:
Frontiers in Bioinformatics, Vol 1 (2022)
The nascent field of microbiome science is transitioning from a descriptive approach of cataloging taxa and functions present in an environment to applying multi-omics methods to investigate microbiome dynamics and function. A large number of new too
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e9ec57f621b474d42c5c1bc948fba4ec
https://pubmed.ncbi.nlm.nih.gov/36303775
https://pubmed.ncbi.nlm.nih.gov/36303775
Autor:
Douglas Mans, David C. Leitch, Robert S. Weber, Jonathan D. Egbert, Lee Edwards, Stacy A. O'Neill-Slawecki, Charles E. Wade, Edwin C. Thomsen
Publikováno v:
Organic Process Research & Development. 23:1803-1812
Electrolysis flow reactors based on the filter-press architecture of redox flow batteries have proven to be effective and scalable toward the production of commercially relevant, pharmaceutical qua...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::64200f5d4617fd9313ff4f7c5e44286d
https://doi.org/10.1021/acs.oprd.8b00379
https://doi.org/10.1021/acs.oprd.8b00379
Publikováno v:
Tetrahedron. 71:5741-5757
A total synthesis of the aglycone of IB-00208 was accomplished in 22 steps using a newly developed approach towards polycyclic 1,4-dioxygenated xanthones from benzocyclobutenones. The generality of this entry to xanthones was initially established on
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8e173a15a193bdd739e2de0779ce981a
https://doi.org/10.1016/j.tet.2015.05.024
https://doi.org/10.1016/j.tet.2015.05.024
Publikováno v:
Organic Letters
Hexacyclic xanthone natural products such as IB-00208 present a formidable challenge in organic synthesis. A new approach to polycyclic 1,4-dioxygenated xanthones from benzocyclobutenones has been developed and applied to the first total synthesis of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f40ba7dc76b60e21aabcbb11475c8474
https://doi.org/10.1021/ol503336t
https://doi.org/10.1021/ol503336t
Publikováno v:
Tetrahedron. 67:6524-6538
We report the first total synthesis of the complex C-aryl glycoside isokidamycin, the epimer of the naturally-occurring pluramycin antibiotic kidamycin. The synthesis features a highly efficientDiels-Alder reaction between a substituted naphthyne and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::61d5857e8349989ef2f9fcceaf658507
https://doi.org/10.1016/j.tet.2011.05.117
https://doi.org/10.1016/j.tet.2011.05.117
Publikováno v:
Tetrahedron Letters. 52:4207-4210
A two-step procedure is described to access 3-alkoxycyclobutanones from chloroacetyl chloride utilizing a step-wise [2+2] ketene cycloaddition followed by catalytic hydrogenation to reduce the α-chlorine in a single reaction sequence. The resulting
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2e2310f9ebf5fce97d279db2cb775453
https://doi.org/10.1016/j.tetlet.2011.06.027
https://doi.org/10.1016/j.tetlet.2011.06.027
Autor:
Douglas Mans, William H. Pearson
Publikováno v:
The Journal of Organic Chemistry. 69:6419-6426
A Kumada cross-coupling reaction involving organomagnesium reagents and (3-methylthio-2-azaallyl)stannanes with a Ni(0) catalyst provided cyclic nonstabilized (2-azaallyl)stannanes in moderate to good yields. Primary alkyl, aryl, and allylic organoma
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3a4e0fcfece0cb28119fa4158b66d3e2
https://doi.org/10.1021/jo049429p
https://doi.org/10.1021/jo049429p
Autor:
William H. Pearson, Douglas Mans
Publikováno v:
Organic Letters. 6:3305-3308
[reaction: see text] The total synthesis of (+)-cocaine is described. An extension of the recently reported proline catalyzed intramolecular enol-exo-aldol reaction to a meso-dialdehyde provided the tropane ring skeleton directly with good enantiomer
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::29b6de757a45b4e17693474cbfb29e33
https://doi.org/10.1021/ol048777a
https://doi.org/10.1021/ol048777a