HFIP in organic synthesis
HF Motiwala, AM Armaly, JG Cacioppo… - Chemical …, 2022 - ACS Publications
1, 1, 1, 3, 3, 3-Hexafluoroisopropanol (HFIP) is a polar, strongly hydrogen bond-donating
solvent that has found numerous uses in organic synthesis due to its ability to stabilize ionic …
solvent that has found numerous uses in organic synthesis due to its ability to stabilize ionic …
[HTML][HTML] Electrocatalysis as an enabling technology for organic synthesis
Electrochemistry has recently gained increased attention as a versatile strategy for
achieving challenging transformations at the forefront of synthetic organic chemistry …
achieving challenging transformations at the forefront of synthetic organic chemistry …
Photons or electrons? A critical comparison of electrochemistry and photoredox catalysis for organic synthesis
NES Tay, D Lehnherr, T Rovis - Chemical reviews, 2021 - ACS Publications
Redox processes are at the heart of synthetic methods that rely on either electrochemistry or
photoredox catalysis, but how do electrochemistry and photoredox catalysis compare? Both …
photoredox catalysis, but how do electrochemistry and photoredox catalysis compare? Both …
Aziridine synthesis by coupling amines and alkenes via an electrogenerated dication
Aziridines—three-membered nitrogen-containing cyclic molecules—are important synthetic
targets. Their substantial ring strain and resultant proclivity towards ring-opening reactions …
targets. Their substantial ring strain and resultant proclivity towards ring-opening reactions …
Recent advances in electrochemically driven radical fluorination and fluoroalkylation
Z Zou, W Zhang, Y Wang, Y Pan - Organic Chemistry Frontiers, 2021 - pubs.rsc.org
Electrochemical fluorination (ECF) refers to the introduction of fluorine-containing moieties
into organic molecules under electrochemical conditions. The primary objective of this …
into organic molecules under electrochemical conditions. The primary objective of this …
Fluorination and fluoroalkylation reactions mediated by hypervalent iodine reagents
ZZ Han, CP Zhang - Advanced Synthesis & Catalysis, 2020 - Wiley Online Library
This review summarizes the progress in the fluorination and fluoroalkylation of electron‐rich
systems with diverse fluorine (F) and fluoroalkyl (Rfn) reagents employing hypervalent …
systems with diverse fluorine (F) and fluoroalkyl (Rfn) reagents employing hypervalent …
Skeletal Ring Contractions via I(I)/I(III) Catalysis: Stereoselective Synthesis of cis-α,α-Difluorocyclopropanes
K Livingstone, K Siebold, S Meyer, V Martín-Heras… - ACS …, 2022 - ACS Publications
The clinical success of α, α-difluorocyclopropanes, combined with limitations in the existing
synthesis portfolio, inspired the development of an operationally simple, organocatalysis …
synthesis portfolio, inspired the development of an operationally simple, organocatalysis …
Electrochemical C− C bond cleavage of cyclopropanes towards the synthesis of 1, 3-difunctionalized molecules
P Peng, X Yan, K Zhang, Z Liu, L Zeng, Y Chen… - Nature …, 2021 - nature.com
Electrochemistry has a lot of inherent advantages in organic synthesis and many redox
reactions have been achieved under electrochemical condition. However, the …
reactions have been achieved under electrochemical condition. However, the …
Expanding organofluorine chemical space: the design of chiral fluorinated isosteres enabled by I (I)/I (III) catalysis
Short aliphatic groups are prevalent in bioactive small molecules and play an essential role
in regulating physicochemistry and molecular recognition phenomena. Delineating their …
in regulating physicochemistry and molecular recognition phenomena. Delineating their …
Iodanyl radical catalysis
Conspectus Hypervalent iodine reagents find application as selective chemical oxidants in a
diverse array of oxidative transformations. The utility of these reagents is often ascribed to …
diverse array of oxidative transformations. The utility of these reagents is often ascribed to …