Zobrazeno 1 - 10
of 247
pro vyhledávání: '"Cyclic Alkenes"'
Publikováno v:
Angewandte Chemie. 133:26536-26540
Difunctionalization of strained cyclic alkynes presents a powerful strategy to build richly functionalized cyclic alkenes in an expedient fashion. Herein we disclose an efficient and flexible approach to achieve carbohalogenation, dicarbofunctionaliz
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Autor:
Hans Gildenast, Damon J. Gilmour, Mitchell R. Perry, Laurel L. Schafer, Savvas G. Hatzikiriakos, Nirmalendu Kuanr, Tanja Tomkovic
Publikováno v:
ACS Applied Polymer Materials. 3:2330-2335
The chemical functionalization of polyolefins to access responsive materials is a long-standing challenge in materials science. Current protocols do not typically tolerate polar functional groups, ...
Publikováno v:
New Journal of Chemistry. 45:10383-10387
A convenient metal-free photocatalytic hydrosilylation of a variety of linear and cyclic alkenes has been investigated. It was found that the free radical type photoinitiator Irgacure 2959 had a better effect on the hydrosilylation reaction; using 3
trans ‐Selective Aryldifluoroalkylation of Endocyclic Enecarbamates and Enamides by Nickel Catalysis
Publikováno v:
Angewandte Chemie International Edition. 59:18741-18747
Efficient methods for the dicarbofuntionalization of the cyclic alkenes 2-pyrroline and 2-azetine are limited. Particularly, the dicarbofunctionalization of endocyclic enecarbamates to achieve fluorinated compounds remains an unsolved issue. Reported
Publikováno v:
ACS Omega, Vol 5, Iss 37, Pp 24033-24044 (2020)
ACS Omega
ACS Omega
A highly stereo- and regioselective synthesis of the core skeleton of hexahydrobenzo[c]phenanthridine-type alkaloids is reported herein for the first time. A wide range of substrate scope, excellent functional group tolerance, and good to excellent y
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::60a8386c0f29b1cbda7c525f5bb0e686
https://doi.org/10.1021/scimeetings.3c00288
https://doi.org/10.1021/scimeetings.3c00288
Publikováno v:
Chemistry Letters. 47:1486-1489
A Cu(I) complex of bisamidine-type sp2N bidentate ligand, Naph-diPIM, catalyzes coupling between 1,3-dicarbonyl compounds and simple cyclic alkenes using (t-BuO)2, providing the corresponding C-all...
Autor:
Paolo Quadrelli, Mattia Moiola, Misal Giuseppe Memeo, Faiq Hamasaid Hussain, Karzan Khaleel Hameed, Ahmed Anwar Amin
Publikováno v:
Synthesis. 51:1383-1390
An easy approach to N-hydroxy-N-cycloalkenylamides, ene adducts of cyclic alkenes of different sizes, is presented. The products can be obtained both through the thermal generation of the nitrosocarbonyl intermediates and via the photochemical fragme
Autor:
Anne-Marie R. Dechert-Schmitt, Christophe Allais, Alex J. Vendola, Robert A. Singer, James P. Morken, James T. Lee
Publikováno v:
Organic letters. 23(8)
The Pt-catalyzed diboration of cyclic alkenes is extended to unsaturated heterocycles and bicyclic compounds and can be accomplished in a diastereoselective fashion. The optimal procedures, substrate scope, and diastereoselectivity were investigated,
Publikováno v:
Journal of the American Chemical Society
We report on the synthesis of an alkane-soluble Zintl cluster, [η4-Ge9(Hyp)3]Rh(COD), that can catalytically hydrogenate cyclic alkenes such as 1,5-cyclooctadiene and cis-cyclooctene. This is the first example of a well-defined Zintl-cluster-based h
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6219ed5a7f092038a105bf4b7758a161
https://eprints.whiterose.ac.uk/166738/3/jacs.0c09742.pdf
https://eprints.whiterose.ac.uk/166738/3/jacs.0c09742.pdf