Zobrazeno 1 - 10
of 58
pro vyhledávání: '"Nicklas Selander"'
Autor:
Linpeng Liu, Yanyu Jian, Weigao Hu, Shaohu Zhao, Zhang-Jie Shi, Nicklas Selander, Taigang Zhou
Publikováno v:
Organic Chemistry Frontiers. 9:3480-3485
A radical cyclization and ring-opening of oxime esters with diselenides was developed.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7771baeeeb89d364f568a6c7e2c3aba8
https://doi.org/10.1039/d2qo00586g
https://doi.org/10.1039/d2qo00586g
Publikováno v:
Organic Letters
A one-pot approach to fluorinated hydroxamic acid, amide, and thioamide derivatives is reported. The reaction proceeds via an N-perfluoroalkylation of nitrosoarenes with perfluoroalkanesulfinates, resulting in labile N-perfluoroalkylated hydroxylamin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::92096b83e7dba968425e559880807432
http://europepmc.org/articles/PMC7311088
http://europepmc.org/articles/PMC7311088
Autor:
Kalman J. Szabo, Nicklas Selander
By presenting novel methods for the efficient preparation of fluorinated compounds and their application in pharmaceutical and agrochemical chemistry as well as medicine, this is a valuable source of information for all researchers in academia and in
Publikováno v:
ACS Catalysis. 7:8441-8445
A nickel-catalyzed 1,2-aminoarylation of oxime-ester-tethered alkenes with boronic acids was developed. A variety of pyrroline derivatives were synthesized in good yields via the successive formation of C(sp3)–N and C(sp3)–C(sp2) bonds. For cyclo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::efbbc2c494e8a6b49b815d65a021d1f4
https://doi.org/10.1021/acscatal.7b03432
https://doi.org/10.1021/acscatal.7b03432
Publikováno v:
Synthesis. 49:4931-4941
The use of a well-chosen catalyst is instrumental for the development of more efficient, economical and environmentally friendly reactions. In recent decades, indium-based catalysts have proven to be competitive and useful alternatives to transition-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a3ac292acce7cc9a282d08d0af166538
https://doi.org/10.1055/s-0036-1588555
https://doi.org/10.1055/s-0036-1588555
Publikováno v:
Angewandte Chemie. 128:12042-12045
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2c109c0c10d9089670c8f2c70dba4629
https://doi.org/10.1002/ange.201606108
https://doi.org/10.1002/ange.201606108
Publikováno v:
Organic letters. 20(12)
A diastereoselective metal-catalyzed reaction of 2-(2-enynyl)pyridines and cyclic enamines is reported. The method provides access to a variety of substituted indolizine derivatives by variation of the enyne component and the reaction conditions. Per
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fbb0721cda3b654ac6e5250eb4ed82f5
https://pubmed.ncbi.nlm.nih.gov/29878789
https://pubmed.ncbi.nlm.nih.gov/29878789
Autor:
Angela van der Werf, Nicklas Selander
Publikováno v:
Organic Letters. 17:6210-6213
The para-selective direct bromination and chlorination of nitrosoarenes with copper(II) bromide and chloride is reported. Under mild reaction conditions, a range of halogenated arylnitroso compounds are obtained in moderate to good yields with high r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ff5a93bf15580eb6b8ad7aad569171ea
https://doi.org/10.1021/acs.orglett.5b03198
https://doi.org/10.1021/acs.orglett.5b03198
Publikováno v:
Chemical communications (Cambridge, England). 53(82)
An intermolecular cyclization of alkynyl enones with cyclic ketones for the synthesis of bicyclo[3.n.1]alkenones is reported. This protocol exhibits a high functional group tolerance and provides access to a variety of bicyclic systems found as skele
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::6243f59b293751f745d6c7298155ea22
https://pubmed.ncbi.nlm.nih.gov/28967928
https://pubmed.ncbi.nlm.nih.gov/28967928
Autor:
Hai-Bin Yang, Nicklas Selander
Publikováno v:
Organicbiomolecular chemistry. 15(8)
A redox-economical strategy for the synthesis of trifluoromethylated enamides using copper catalysis is reported. The reaction employs the inexpensive Langlois reagent (CF3SO2Na) and takes place without the need of an external oxidant. The trifluorom
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3dceafdb266549ec7e06f9888f242224
https://pubmed.ncbi.nlm.nih.gov/28155956
https://pubmed.ncbi.nlm.nih.gov/28155956