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 …

Advances in 2H-azirine chemistry: A seven-year update

AF Khlebnikov, MS Novikov, NV Rostovskii - Tetrahedron, 2019 - Elsevier
Abstract 2H-Azirines are versatile building blocks for the preparation of various nitrogen-
containing heterocycles. Seven years ago the comprehensive review on azirine chemistry …

Copper (I)-Catalyzed Late-Stage Introduction of Oxime Ethers into Peptides at the Carboxylic Acid Site

Y Liu, Z He, W Ma, G Bao, Y Li, C Yu, J Li, RE… - Organic …, 2022 - ACS Publications
We have developed a method of introducing biological oxime ether fragments into peptides
by CuI-catalyzed late-stage modification and functionalization of peptides, utilizing their acid …

Silver-catalysed C–H bond activation: a recent review

S Radhika, CMA Abdulla, T Aneeja… - New Journal of …, 2021 - pubs.rsc.org
Transition metal catalysed C–H activations are efficient, simple, mild, cost-effective and
stereoselective, and many of them are environmentally sustainable transformations. These …

2H‐Azirines: Recent Progress in Synthesis and Applications

F Xu, FW Zeng, WJ Luo, SY Zhang… - European Journal of …, 2024 - Wiley Online Library
Abstract 2H‐arizines are important three‐membered heterocycles in organic chemistry.
Recently, many advances in the synthesis and functionalization of 2H‐arizines have been …

2H-Azirines as C–C Annulation Reagents in Cu-Catalyzed Synthesis of Furo[3,2-c]quinolone Derivatives

PA Sakharov, NV Rostovskii, AF Khlebnikov… - Organic …, 2019 - ACS Publications
A method of furo-annulation of 4-hydroxy-2-oxoquinoline-3-carboxylates with 3-arylazirines
under Cu (II) catalysis was developed to synthesize a variety of 2, 3-dihydrofuro [3, 2-c] …

Visible Light‐Induced, Metal‐Free Denitrative [3+ 2] Cycloaddition for Trisubstituted Pyrrole Synthesis

BS Karki, L Devi, A Pokhriyal, R Kant… - Chemistry–An Asian …, 2019 - Wiley Online Library
A metal‐free, regioselective synthesis of trisubstituted pyrroles has been developed through
a formal [3+ 2] cycloaddition reaction between 2H‐azirines and nitroalkenes under visible …

Rhodium (III)-catalyzed chemoselective C–H functionalization of benzamides with methyleneoxetanones controlled by the solvent

M Bian, K Ma, H Mawjuda, X Yu, X Li, H Gao… - Organic & …, 2019 - pubs.rsc.org
Described herein is a Rh (III)-catalyzed and solvent-controlled double C–H functionalization
of common benzamides via selective acyl C–O cleavage (β-H elimination) or alkyl C–O …

An Unconventional trans-exo-Selective Cyclization of Alkyne-Tethered Cyclohexadienones Initiated by Rhodium(III)-Catalyzed C–H Activation via Insertion Relay

YX Tan, XY Liu, SQ Zhang, PP Xie, X Wang… - CCS …, 2021 - chinesechemsoc.org
Different from the established trans-endo-selective cyclization of alkyne-tethered
electrophiles that involve an E/Z isomerization process, herein, the authors present a novel …

Rhodium(III)‐Catalyzed Sequential C−H Activation and Cyclization from N‐Methoxyarylamides and 3‐Diazooxindoles for the Synthesis of Isochromenoindolones

GH Ko, C Maeng, H Jeong, SH Han… - Chemistry–An Asian …, 2021 - Wiley Online Library
An efficient synthetic method for structurally various isochromenoindolones has been
demonstrated through Rh (III)‐catalyzed C− H activation followed by a cyclization reaction of …