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pro vyhledávání: '"Taylor M. Sodano"'
Publikováno v:
Chemical Science. 13:11721-11737
The unique chemistry of small, strained carbocyclic systems has long captivated organic chemists from a theoretical and fundamental standpoint. A resurgence of interest in strained carbocyclic species has been prompted by their potential as bioisoste
Publikováno v:
ACS Med Chem Lett
[Image: see text] Many promising drug candidates and pharmaceutical compounds fail due to idiosyncratic adverse drug reactions (IADRs), often arising from the formation of reactive metabolites. Among the “structural alerts” responsible, anilines
Autor:
Taylor M. Sodano, Daryl Staveness, Kangjun Li, Elizabeth A. Burnham, Klarissa D. Jackson, Corey R. J. Stephenson
Publikováno v:
Chem. 5:215-226
Summary This report describes the photochemical conversion of aminocyclopropanes into 1-aminonorbornanes via formal [3 + 2] cycloadditions initiated by homolytic fragmentation of amine radical cation intermediates. Aligning with the modern movement t
Autor:
Brandon W. Alexander, Emilia J. Groso, Alexander N. Golonka, Ryan A. Harding, Taylor M. Sodano, Corinna S. Schindler
Publikováno v:
ACS Catalysis. 8:2006-2011
Herein, we describe the development of a synthetic strategy towards chiral 3-pyrrolines based on the design principle of iron(III)-catalyzed carbonyl-olefin metathesis. This approach takes advantage of commercially available amino acids as chiral poo
This report describes a new route toward 1‑aminonorbornanes via strain-driven, visible light-mediated formal [3+2] cycloadditions with aminocyclopropanes. Lewis acidic salts (LiBF4, ZnCl2) were found to facilitate the oxidation of a variety of amin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::708281c723de186ebe4312775e254d49
https://doi.org/10.26434/chemrxiv.5437255.v1
https://doi.org/10.26434/chemrxiv.5437255.v1