Zobrazeno 1 - 10
of 148
pro vyhledávání: '"C. Virgil"'
Publikováno v:
Scientific Drilling, Vol 9, Pp 37-40 (2010)
No abstract available. doi:10.2204/iodp.sd.9.07.2010
Externí odkaz:
https://doaj.org/article/5a13f6d1b4594cc58c98adcca49f7d72
Publikováno v:
In Additive Manufacturing May 2018 21:579-588
Publikováno v:
Journal of the American Chemical Society. 145:7763-7767
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::debcf945155c1a16b8b0325ead7b8e4e
https://doi.org/10.1021/jacs.3c02142
https://doi.org/10.1021/jacs.3c02142
Autor:
Alexander W. Rand, Kevin J. Gonzalez, Christopher E. Reimann, Scott C. Virgil, Brian M. Stoltz
Publikováno v:
Journal of the American Chemical Society. 145:7278-7287
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e57805dfccebe07ef6a592a07f0a8f34
https://doi.org/10.1021/jacs.2c13146
https://doi.org/10.1021/jacs.2c13146
Autor:
Nicholas J. Hafeman, Steven A. Loskot, Christopher E. Reimann, Beau P. Pritchett, Scott C. Virgil, Brian M. Stoltz
Publikováno v:
Chemical Science. 14:4745-4758
The complete account of the total syntheses of scabrolide A and yonarolide is disclosed. This article describes an initial approach involving a bio-inspired macrocyclization/transannular Diels–Alder cascade, which ultimately failed due to undesired
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3c6bc51de2cbabc624817d4e26f6a480
https://doi.org/10.1039/d3sc00651d
https://doi.org/10.1039/d3sc00651d
Autor:
Tianyi Zhang, Alexander Q. Cusumano, Nicholas J. Hafeman, Steven A. Loskot, Christopher E. Reimann, Scott C. Virgil, William A. Goddard, Brian M. Stoltz
Publikováno v:
The Journal of Organic Chemistry. 87:14115-14124
We utilize ab initio quantum mechanics calculations to evaluate a range of plausible mechanistic pathways for the unexpected formation of a [6-4-4] ring system from an enone-olefin photocycloaddition in the synthesis of (-)-scabrolide A, previously r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5f5575e8abe3483a6f619867fde2b108
https://doi.org/10.1021/acs.joc.2c01693
https://doi.org/10.1021/acs.joc.2c01693
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Autor:
C Virgil Solomon
Publikováno v:
Microscopy and Microanalysis. 28:2954-2956
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::70c74a4320e6390147dc08388d32102f
https://doi.org/10.1017/s1431927622011072
https://doi.org/10.1017/s1431927622011072
Autor:
Nicholas J. Hafeman, Melinda Chan, Tyler J. Fulton, Eric J. Alexy, Steven A. Loskot, Scott. C. Virgil, Brian M. Stoltz
Publikováno v:
Journal of the American Chemical Society. 144(44)
The first total synthesis of the furanobutenolide-derived cembranoid diterpenoid havellockate is disclosed. Our convergent strategy employs a Julia-Kocienski olefination to join two enantioenriched fragments to produce a diene that is subsequently us
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5c22e72ce3b69f3100fc9ef780d2d45b
https://pubmed.ncbi.nlm.nih.gov/36287147
https://pubmed.ncbi.nlm.nih.gov/36287147
Autor:
Yiyang Liu, Marc Liniger, Ryan M. McFadden, Jenny L. Roizen, Jacquie Malette, Corey M. Reeves, Douglas C. Behenna, Masaki Seto, Jimin Kim, Justin T. Mohr, Scott C. Virgil, Brian M. Stoltz
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 10, Iss 1, Pp 2501-2512 (2014)
Pd-catalyzed enantioselective alkylation in conjunction with further synthetic elaboration enables the formal total syntheses of a number of “classic” natural product target molecules. This publication highlights recent methods for setting quater
Externí odkaz:
https://doaj.org/article/53aff6b2b8524eb8bcb18875eaef6ba1