Fluorine and fluorinated motifs in the design and application of bioisosteres for drug design
NA Meanwell - Journal of medicinal chemistry, 2018 - ACS Publications
The electronic properties and relatively small size of fluorine endow it with considerable
versatility as a bioisostere and it has found application as a substitute for lone pairs of …
versatility as a bioisostere and it has found application as a substitute for lone pairs of …
Preparation and utility of organic pentafluorosulfanyl-containing compounds
PR Savoie, JT Welch - Chemical reviews, 2015 - ACS Publications
The organic chemistry of the pentafluorosulfanyl (SF5) group, previously reviewed 1 and
extensively developed by Gard, has only recently come under more widespread …
extensively developed by Gard, has only recently come under more widespread …
The TV in your pocket: development of liquid‐crystal materials for the new millennium
New liquid crystals with very low viscosity, good mesophase behavior, and high reliability
are necessary to achieve the breakthrough from flat computer monitors to large displays for …
are necessary to achieve the breakthrough from flat computer monitors to large displays for …
(Hetero)aryl‐SVI Fluorides: Synthetic Development and Opportunities
Abstract (Hetero) arylsulfur compounds where the S atom is in the oxidation state VI
represent a large percentage of the molecular functionalities present in organic chemistry …
represent a large percentage of the molecular functionalities present in organic chemistry …
Synthetic chemistry and biological activity of pentafluorosulphanyl (SF5) organic molecules
S Altomonte, M Zanda - Journal of Fluorine Chemistry, 2012 - Elsevier
The pentafluorosulphanyl group (SF5) is a highly stable chemical function which has been
attracting a great deal of interest owing to its peculiar chemical, structural, physicochemical …
attracting a great deal of interest owing to its peculiar chemical, structural, physicochemical …
Chemistry of Pentafluorosulfanyl Derivatives and Related Analogs: From Synthesis to Applications
R Kordnezhadian, BY Li, A Zogu… - … A European Journal, 2022 - Wiley Online Library
Abstract Pentafluorosulfanyl (SF5)‐containing compounds and corresponding analogs are a
highly valuable class of fluorine‐containing building blocks owing to their unique properties …
highly valuable class of fluorine‐containing building blocks owing to their unique properties …
Application of the pentafluorosulfanyl group as a bioisosteric replacement
MF Sowaileh, RA Hazlitt, DA Colby - ChemMedChem, 2017 - Wiley Online Library
The success of fluorinated molecules in drug design has led medicinal chemists to search
for new fluorine‐containing substituents. A major recently developed group is the …
for new fluorine‐containing substituents. A major recently developed group is the …
[HTML][HTML] Discovery of practical production processes for arylsulfur pentafluorides and their higher homologues, bis-and tris (sulfur pentafluorides): Beginning of a new …
T Umemoto, LM Garrick, N Saito - Beilstein journal of organic …, 2012 - beilstein-journals.org
Various arylsulfur pentafluorides, ArSF 5, have long been desired in both academic and
industrial areas, and ArSF 5 compounds have attracted considerable interest in many areas …
industrial areas, and ArSF 5 compounds have attracted considerable interest in many areas …
Making the SF5 Group More Accessible: A Gas‐Reagent‐Free Approach to Aryl Tetrafluoro‐λ6‐sulfanyl Chlorides
CR Pitts, D Bornemann, P Liebing… - Angewandte Chemie …, 2019 - Wiley Online Library
Modern pentafluorosulfanyl (SF5) chemistry has an Achilles heel: synthetic accessibility.
Herein, we present the first approach to aryl‐SF4Cl compounds (key intermediates in state …
Herein, we present the first approach to aryl‐SF4Cl compounds (key intermediates in state …
Synthesis of pentafluorosulfanylpyrazole and pentafluorosulfanyl-1, 2, 3-triazole and their derivatives as energetic materials by click chemistry
C Ye, GL Gard, RW Winter, RG Syvret, B Twamley… - Organic …, 2007 - ACS Publications
1-Pentafluorosulfanyl acetylene and its derivatives react with azide or diazomethane giving
rise to an SF5-substituted 1, 2, 3-triazole or pyrazole. The SF5 group increases density …
rise to an SF5-substituted 1, 2, 3-triazole or pyrazole. The SF5 group increases density …