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BINOL Modification via SnAr Reactions with Pentafluoropyridine Full article

Journal Mendeleev Communications
ISSN: 0959-9436 , E-ISSN: 1364-551X
Output data Year: 2015, Volume: 25, Number: 1, Pages: 39-40 Pages count : 2 DOI: 10.1016/j.mencom.2015.01.014
Tags CATALYSIS; LIGANDS
Authors Koltunov Konstantin Yu. 1,2 , Chernov Aleksey N. 2,3
Affiliations
1 G.K.Boreskov Institute of Catalysis, Siberian Branch of teh Russian Academy of Sciences
2 Department of Natutral Sciences, Novosibirsk State University
3 V.S. Sobolev Institute of Geology and Mineralogy SB RAS

Abstract: (R)- and (S)-binaphthyl-2,2’-diols (BINOLs) smoothly react with pentafluoropyridine without racemization to give (R)- and (S)-2,2’- bis(tetrafluoropyridin-4-yloxy)-1,1’-binaphthyls. The 2(6)-positioned pyridine fluorine atoms can be replaced with amino moieties by reactions with amines.
Cite: Koltunov K.Y. , Chernov A.N.
BINOL Modification via SnAr Reactions with Pentafluoropyridine
Mendeleev Communications. 2015. V.25. N1. P.39-40. DOI: 10.1016/j.mencom.2015.01.014 WOS Scopus РИНЦ ANCAN OpenAlex
Dates:
Submitted: Mar 31, 2014
Published print: Jan 1, 2015
Published online: Jan 28, 2015
Identifiers:
Web of science: WOS:000349879400014
Scopus: 2-s2.0-84921862175
Elibrary: 23969994
Chemical Abstracts: 2015:222757
Chemical Abstracts (print): 162:327046
OpenAlex: W2040836298
Citing:
DB Citing
Web of science 6
Scopus 7
Elibrary 5
OpenAlex 6
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