Zobrazeno 1 - 10
of 38
pro vyhledávání: '"Bedermann A"'
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Autor:
Bédard, Anne-Catherine, Adamo, Andrea, Aroh, Kosi C., Russell, M. Grace, Bedermann, Aaron A., Torosian, Jeremy, Yue, Brian, Jensen, Klavs F., Jamison, Timothy F.
Publikováno v:
Science, 2018 Sep . 361(6408), 1220-1225.
Externí odkaz:
https://www.jstor.org/stable/26565593
Publikováno v:
Organic Process Research & Development. 23:278-282
The use of strong organometallic bases and nucleophiles is commonplace in modern organic synthesis. That they react with a wide range of functional groups requires accurate and precise stoichiometry in reactions that utilize them. For best results, t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dca3aa79ab3674d333043994fe481b83
https://doi.org/10.1021/acs.oprd.8b00434
https://doi.org/10.1021/acs.oprd.8b00434
Autor:
Leung, Joyce C.1, Bedermann, Aaron A.1, Njardarson, Jón T.1, Spiegel, David A.1, Murphy, Graham K.1, Hama, Naoto1, Twenter, Barry M.1, Dong, Ping1, Shirahata, Tatsuya1, McDonald, Ivar M.1, Inoue, Munenori1, Taniguchi, Nobuaki1, McMahon, Travis C.1, Schneider, Christopher M.1, Tao, Nancy1, Stoltz, Brian M.1, Wood, John L.1 john_l_wood@baylor.edu
Publikováno v:
Angewandte Chemie. 2/12/2018, Vol. 130 Issue 7, p2009-2012. 4p.
Autor:
Naoto Hama, John L. Wood, Nobuaki Taniguchi, Joyce C. Leung, Graham K. Murphy, Ivar M. McDonald, Tatsuya Shirahata, David A. Spiegel, Aaron A. Bedermann, Travis C. McMahon, Christopher M. Schneider, Ping Dong, Nancy Tao, Munenori Inoue, Jon T. Njardarson, Barry M. Twenter, Brian M. Stoltz
Publikováno v:
Angewandte Chemie. 130:2009-2012
Described herein is a synthetic strategy for the total synthesis of (±)-phomoidride D. This highly efficient and stereoselective approach provides rapid assembly of the carbocyclic core by way of a tandem phenolic oxidation/intramolecular Diels-Alde
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a7eb01021b7c3f45cf10b171a76e43bc
https://doi.org/10.1002/ange.201712369
https://doi.org/10.1002/ange.201712369
Autor:
Andrea Adamo, Kosi C. Aroh, Brian Yue, M. Grace Russell, Aaron A. Bedermann, Anne-Catherine Bédard, Timothy F. Jamison, Jeremy Torosian, Klavs F. Jensen
Publikováno v:
Science (New York, N.Y.). 361(6408)
A self-optimizing reactor Chemists spend a great deal of time tweaking the conditions of known reactions. Small changes to temperature and concentration can have a big influence over product yield. Bédard et al. present a flow-based reaction platfor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1b490c5f039b596c903239ae60fdf5bb
https://pubmed.ncbi.nlm.nih.gov/30237351
https://pubmed.ncbi.nlm.nih.gov/30237351
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Autor:
Ran N. Tao, Naoto Hama, Christopher M. Schneider, Ping Dong, Aaron Bedermann, Graham K. Murphy, Barry M. Twenter, Travis C. McMahon, David Spiegel, John L. Wood
Publikováno v:
Organic Letters. 14:4544-4547
The carbocyclic core of the phomoidrides has been synthesized efficiently and in high yield. Key steps include a phenolic oxidation/intramolecular Diels-Alder sequence, tandem radical cyclization, and a late-stage Wharton fragmentation of a densely f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::84eb45ff97f72568e24bd639e5fb7bcb
https://doi.org/10.1021/ol302011b
https://doi.org/10.1021/ol302011b
Autor:
Naoto Hama, Nobuaki Taniguchi, Tatsuya Shirahata, Travis C. McMahon, John L. Wood, Ivar M. McDonald, Barry M. Twenter, Ping Dong, Graham K. Murphy, David Spiegel, Munenori Inoue, Aaron Bedermann
Publikováno v:
The Journal of organic chemistry. 78(2)
An efficient and highly stereoselective approach toward the phomoidride family of natural products is described. The carbocyclic core structure was assembled using a tandem phenolic oxidation/Diels–Alder cycloaddition and a tandem 5-exo-trig/5-exo-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9267a66dc62153891c66918eb9112378
https://pubmed.ncbi.nlm.nih.gov/23245580
https://pubmed.ncbi.nlm.nih.gov/23245580