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Applications of domino transformations in organic synthesis. Volume 1. / S. A. Snyder, E. Schaumann, editors. [elektronicky zdroj]

Externí odkaz: Kolekce e-knih KNAV

Micelle-enabled self-assembly of porous and monolithic carbon membranes for bioelectronic interfaces.

Autor: Fang Y; Department of Chemistry, University of Chicago, Chicago, IL, USA. yinfang@nano-theranostic.com., Prominski A; Department of Chemistry, University of Chicago, Chicago, IL, USA.; The James Franck Institute, University of Chicago, Chicago, IL, USA., Rotenberg MY; The James Franck Institute, University of Chicago, Chicago, IL, USA., Meng L; Pritzker School of Molecular Engineering, University of Chicago, Chicago, IL, USA., Acarón Ledesma H; The Graduate Program in Biophysical Sciences, University of Chicago, Chicago, IL, USA., Lv Y; The James Franck Institute, University of Chicago, Chicago, IL, USA., Yue J; Department of Chemistry, University of Chicago, Chicago, IL, USA., Schaumann E; Department of Chemistry, University of Chicago, Chicago, IL, USA.; The James Franck Institute, University of Chicago, Chicago, IL, USA., Jeong J; Department of Computer Science, University of Chicago, Chicago, IL, USA., Yamamoto N; Department of Chemistry, University of Chicago, Chicago, IL, USA., Jiang Y; Department of Chemistry, University of Chicago, Chicago, IL, USA.; The James Franck Institute, University of Chicago, Chicago, IL, USA., Elbaz B; The Division of Multiple Sclerosis and Neuroimmunology, Feinberg School of Medicine, Northwestern University, Chicago, IL, USA., Wei W; Department of Neurobiology, University of Chicago, Chicago, IL, USA., Tian B; Department of Chemistry, University of Chicago, Chicago, IL, USA. btian@uchicago.edu.; The James Franck Institute, University of Chicago, Chicago, IL, USA. btian@uchicago.edu.; Institute for Biophysical Dynamics, University of Chicago, Chicago, IL, USA. btian@uchicago.edu.

Publikováno v: Nature nanotechnology [Nat Nanotechnol] 2021 Feb; Vol. 16 (2), pp. 206-213. Date of Electronic Publication: 2020 Dec 07.

New syntheses and ring expansion reactions of cyclobutenimines

Autor: Schaumann, E, Oppermann, G, Stranberg, M, Moore, HW

Publikováno v: Schaumann, E; Oppermann, G; Stranberg, M; & Moore, HW. (2010). New syntheses and ring expansion reactions of cyclobutenimines. Australian Journal of Chemistry, 63(12), 1656-1664. doi: 10.1071/CH10318. UC Irvine: Retrieved from: http://www.escholarship.org/uc/item/0z66q3k1

Two routes are reported for the synthesis of iminocyclobutenones having N-(het)aryl substitution: an addition/substitution sequence starting with cyclobutenediones and an aza-Wittig method. A new synthetic route to N-alkyl derivatives is also present

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od_______325::c799ebb90d6d15d124965d218ad50ed7
http://www.escholarship.org/uc/item/0z66q3k1

Exclusive Solvent-Controlled Regioselective Catalytic Synthesis of Potentially Bioactive Imidazolidineiminodithiones: NMR Analysis, Computational Studies and X-ray Crystal Structures.

Autor: Moussa, Ziad¹ (AUTHOR) 202102195@uaeu.ac.ae, Saada, Sara¹ (AUTHOR) 202050063@uaeu.ac.ae, Paz, Alejandro Perez¹ (AUTHOR) zmoussa@uaeu.ac.ae, Alzamly, Ahmed¹ (AUTHOR), Judeh, Zaher M. A.² (AUTHOR), Alshehhi, Aaesha R.¹ (AUTHOR), Khudhair, Aisha¹ (AUTHOR), Almheiri, Salama A.¹ (AUTHOR), Al-Masri, Harbi Tomah³ (AUTHOR), Ahmed, Saleh A.⁴ (AUTHOR) zmoussa@uaeu.ac.ae

Publikováno v: Molecules. Aug2024, Vol. 29 Issue 16, p3958. 27p.