BINOL Modification via SnAr Reactions with Pentafluoropyridine Full article
Journal |
Mendeleev Communications
ISSN: 0959-9436 , E-ISSN: 1364-551X |
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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 | ||||||
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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
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 |