Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Mark A. Maskeri"'
Publikováno v:
Journal of the American Chemical Society. 144:23358-23367
Keteniminium ions, the nitrogen analogues of ketenes, exhibit high reactivity toward olefins and π-systems. Previous results from the Maulide group demonstrated an unexpected propensity for an alternative intramolecular Belluš-Claisen-type rearrang
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::20010cd4fc80a0a8dbd23fef4e00b6f4
https://doi.org/10.1021/jacs.2c09146
https://doi.org/10.1021/jacs.2c09146
Autor:
Rosa V. Espinoza, Mark A. Maskeri, Aneta Turlik, Anjanay Nangia, Yogan Khatri, John Montgomery, K. N. Houk, David H. Sherman
Publikováno v:
ACS Catalysis. 12:3731-3742
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cf00e0758d9fdeec4fe6954760ee757a
https://doi.org/10.1021/acscatal.2c00364
https://doi.org/10.1021/acscatal.2c00364
Publikováno v:
Angewandte Chemie (International Ed. in English)
Angewandte Chemie (International ed. in English), vol 60, iss 15
Angewandte Chemie (International ed. in English), vol 60, iss 15
Previous studies showed that the FeII/α‐ketoglutarate dependent dioxygenase AsqJ induces a skeletal rearrangement in viridicatin biosynthesis in Aspergillus nidulans, generating a quinolone scaffold from benzo[1,4]diazepine‐2,5‐dione substrate
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5a17113512073a43015720906dfdaf3e
http://europepmc.org/articles/PMC8049060
http://europepmc.org/articles/PMC8049060
A Sequential Umpolung /Enzymatic Dynamic Kinetic Resolution Strategy for the Synthesis of γ‐Lactones
Publikováno v:
Chemistry
Combining biological and small-molecule catalysts under a chemoenzymatic manifold presents a series of significant advantages to the synthetic community. We report herein the successful development of a two-step/single flask synthesis of γ-lactones
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::18b88283e4bc72ea3dd644bb28be2ff1
https://doi.org/10.1002/chem.202000747
https://doi.org/10.1002/chem.202000747
Computational Exploration of Anomalous Regioselectivities in Cycloadditions of Ketenes to Oxazolines
Publikováno v:
The Journal of organic chemistry. 87(5)
Thermal (2 + 2) cycloadditions of several
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6431272f9fff81737b48485dffa2d7b6
https://pubmed.ncbi.nlm.nih.gov/35076243
https://pubmed.ncbi.nlm.nih.gov/35076243
Autor:
Mark A. Maskeri, Aneta Turlik, David H. Sherman, John Montgomery, Yogan Khatri, Rosa V. Espinoza, K. N. Houk, Anjanay Nangia
P450-catalyzed hydroxylation reactions are well understood mechanistically including the identity of the active oxidizing species. However, the catalytically active heme-iron species in P450 iterative oxidation cascades that involve mechanistically d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e0a65835ce7da0d52cb764417b6f2eb6
https://doi.org/10.26434/chemrxiv-2021-9q343
https://doi.org/10.26434/chemrxiv-2021-9q343
Autor:
Mark A. Maskeri, Karl A. Scheidt, Daniel M. Walden, Taisiia Feoktistova, Matthew J. O'Connor, Alexander C. Brueckner, Paul Ha-Yeon Cheong
Publikováno v:
Chemical Science
Enantioselective additions to oxocarbenium ions are high-value synthetic transformations but have proven challenging to achieve. In particular, the oxa-Pictet–Spengler reaction has only recently been rendered enantioselective. We report experimenta
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::04434603607d706198a8df76e60b49ca
https://pubmed.ncbi.nlm.nih.gov/34123127
https://pubmed.ncbi.nlm.nih.gov/34123127
Publikováno v:
Angewandte Chemie (International ed. in English). 57(52)
Carbocations stabilized by adjacent oxygen atoms are useful reactive intermediates involved in fundamental chemical transformations. These oxocarbenium ions typically lack sufficient electron density to engage established chiral Bronsted or Lewis aci
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::579dc618f34771d6429ecc4fdff8f864
https://pubmed.ncbi.nlm.nih.gov/30380196
https://pubmed.ncbi.nlm.nih.gov/30380196