Nitrile-containing pharmaceuticals: target, mechanism of action, and their SAR studies
X Wang, Y Wang, X Li, Z Yu, C Song, Y Du - RSC medicinal chemistry, 2021 - pubs.rsc.org
The nitrile group is an important functional group widely found in both pharmaceutical
agents and natural products. More than 30 nitrile-containing pharmaceuticals have been …
agents and natural products. More than 30 nitrile-containing pharmaceuticals have been …
19F NMR as a tool in chemical biology
We previously reviewed the use of 19 F NMR in the broad field of chemical biology [Cobb,
SL; Murphy, CD J. Fluorine Chem. 2009, 130, 132–140] and present here a summary of the …
SL; Murphy, CD J. Fluorine Chem. 2009, 130, 132–140] and present here a summary of the …
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 …
Recent advances in the synthesis and medicinal chemistry of SF5 and SF4Cl compounds
M Sani, M Zanda - Synthesis, 2022 - thieme-connect.com
This short review covers the most important advances published in the literature during the
last five years, concerning the synthesis, chemical modifications, and applications of SF 5 …
last five years, concerning the synthesis, chemical modifications, and applications of SF 5 …
Synthesis of Sterically Hindered α-Hydroxycarbonyls through Radical–Radical Coupling
K Ota, K Nagao, H Ohmiya - Organic Letters, 2021 - ACS Publications
We describe a synthetic approach to sterically hindered α-hydroxy carbonyl compounds
through radical–radical coupling. An organic photoredox catalysis reaction converts an …
through radical–radical coupling. An organic photoredox catalysis reaction converts an …
Photochemical Activation of Sulfur Hexafluoride: A Tool for Fluorination and Pentafluorosulfanylation Reactions
D Rombach, HA Wagenknecht - Synthesis, 2022 - thieme-connect.com
The photoactivation of notoriously inert sulfur hexafluoride represents a challenge for
photochemistry. This short review summarizes recently published efforts and the …
photochemistry. This short review summarizes recently published efforts and the …
Radical Addition of SF5Cl to Cyclopropenes: Synthesis of (Pentafluorosulfanyl)cyclopropanes
G Lefebvre, O Charron, J Cossy, C Meyer - Organic Letters, 2021 - ACS Publications
With the goal of accessing yet unknown SF5-cyclopropyl building blocks, the radical addition
of SF5Cl to cyclopropenes was investigated. Addition of the SF5 radical occurs …
of SF5Cl to cyclopropenes was investigated. Addition of the SF5 radical occurs …
Electron donor-acceptor (EDA)-complex enabled SF5Cl addition on alkenes and alkynes
A Gilbert, M Birepinte, JF Paquin - Journal of Fluorine Chemistry, 2021 - Elsevier
A new method for the addition of SF 5 Cl on unsaturated compounds was developed, based
on the use of an electron donor-acceptor (EDA)-complex and visible light irradiation. The …
on the use of an electron donor-acceptor (EDA)-complex and visible light irradiation. The …
Hydrothiolation of Triisopropylsilyl Acetylene Sulfur Pentafluoride – Charting the Chemical Space of β‐SF5 Vinyl Sulfides
Recently, we suggested liquid and high‐boiling TIPS‐CC‐SF5 (TASP) as a versatile reagent
to access so far elusive SF5‐containing building blocks by less specialized laboratories …
to access so far elusive SF5‐containing building blocks by less specialized laboratories …
Metal‐Catalyst‐Free One‐Pot Aqueous Synthesis of trans‐1,2‐Diols from Electron‐Deficient α,β‐Unsaturated Amides via Epoxidation Using Oxone as a Dual Role …
MZ Zhang, P Wang, HY Liu, D Wang, Y Deng… - …, 2023 - Wiley Online Library
In organic synthesis, incorporating two functional groups into the carbon‐carbon double
bond of α, β‐unsaturated amides is challenging due to the electron‐deficient nature of the …
bond of α, β‐unsaturated amides is challenging due to the electron‐deficient nature of the …