Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Aran K. Hubbell"'
Autor:
Robert A. Singer, Sebastien Monfette, David Bernhardson, Sergei Tcyrulnikov, Aran K. Hubbell, Eric C. Hansen
Publikováno v:
Organic Process Research & Development. 25:1802-1815
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d429612716da3657b42aba7905ac63c8
https://doi.org/10.1021/acs.oprd.1c00241
https://doi.org/10.1021/acs.oprd.1c00241
Autor:
Aran K. Hubbell, Jessica R. Lamb, Samantha N. MacMillan, Kristine Klimovica, Geoffrey W. Coates, Timothy D. Shaffer, Michael Mulzer
Publikováno v:
ACS Catalysis. 10:12537-12543
Poly(pivalolactone) (PPVL) is a crystalline polyester with attractive physical and mechanical properties; however, prohibitively expensive syntheses of pivalolactone have thwarted efforts to produc...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dee88ac08a8abf3c0294f0ad683a5780
https://doi.org/10.1021/acscatal.0c03492
https://doi.org/10.1021/acscatal.0c03492
Publikováno v:
Journal of the American Chemical Society. 142:8029-8035
Reactions facilitating inversion of alkene stereochemistry are rare, sought-after transformations in the field of modern organic synthesis. Although a number of isomerization reactions exist, most methods require specific, highly activated substrates
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e8c173e61700a8e09d6a2e520fe0a68e
https://doi.org/10.1021/jacs.0c02653
https://doi.org/10.1021/jacs.0c02653
Autor:
Aran K. Hubbell, Sebastian Torker, Damián Padín Santos, Yuebiao Zhou, Filippo Romiti, Amir H. Hoveyda, Kevin P. McGrath
Publikováno v:
Advanced Synthesis & Catalysis. 362:370-375
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a07e16f83f2164a279792b76ef5b66b5
https://doi.org/10.1002/adsc.201901435
https://doi.org/10.1002/adsc.201901435
Autor:
Geoffrey W. Coates, Aran K. Hubbell
Publikováno v:
The Journal of organic chemistry. 85(21)
Due to their inherent ring strain and electrophilicity, epoxides are highly attractive building blocks for fundamental organic reactions. However, controlling the regioselectivity of disubstituted epoxide transformations is often particularly challen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9cec9474836758cc8e843d8eb1d0ef61
https://pubmed.ncbi.nlm.nih.gov/33076663
https://pubmed.ncbi.nlm.nih.gov/33076663
Publikováno v:
Journal of the American Chemical Society. 141(6)
We report the regioselective carbonylation of 2,2-disubstituted epoxides to β,β-disubstituted β-lactones. Mechanistic studies revealed epoxide ring-opening as the turnover limiting step, an insight that facilitated the development of improved reac
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::37bf9a25565475b99b09d4d1c691649b
https://pubmed.ncbi.nlm.nih.gov/30707018
https://pubmed.ncbi.nlm.nih.gov/30707018