Recent advances in the synthetic application of difluorocarbene

C Ni, J Hu - Synthesis, 2014 - thieme-connect.com
Difluorocarbene is a versatile, reactive intermediate for use in organic synthesis. Over the
past decade, significant progress has been made in difluorocarbene chemistry owing to the …

Proline Analogues

V Kubyshkin, M Rubini - Chemical Reviews, 2024 - ACS Publications
Within the canonical repertoire of the amino acid involved in protein biogenesis, proline
plays a unique role as an amino acid presenting a modified backbone rather than a side …

Electronically Ambivalent Hydrodefluorination of Aryl‐CF3 groups enabled by Electrochemical Deep‐Reduction on a Ni Cathode

JR Box, ME Avanthay, DL Poole… - Angewandte Chemie …, 2023 - Wiley Online Library
Abstract The Ar‐CF2H moiety is featured in an increasing number of bioactive compounds
due to its unique combination of properties. The hydrodefluorination of Ar‐CF3 compounds …

Difluoro-substituted bicyclo [1.1. 1] pentanes for medicinal chemistry: design, synthesis, and characterization

RM Bychek, V Hutskalova, YP Bas… - The Journal of …, 2019 - ACS Publications
A practical synthetic approach to the difluoro-substituted bicyclo [1.1. 1] pentanes was
developed. The key step was an addition of difluorocarbene (: CF2) to electron-rich bicyclo …

Recent developments in trifluoromethylation or difluoroalkylation by use of difluorinated phosphonium salts

C Zhang - Advanced Synthesis & Catalysis, 2017 - Wiley Online Library
Recent advances in trifluoromethylation or difluoroalkylation reactions by use of
difluorinated phosphonium salts are summarized. In the presence of base, water …

Fluorinated prolines as conformational tools and reporters for peptide and protein chemistry

SJM Verhoork, PM Killoran, CR Coxon - Biochemistry, 2018 - ACS Publications
Amide bonds at the proline nitrogen are particularly susceptible to rotation, affording cis and
trans isomers. Installation of a stereochemically defined electron-withdrawing fluorine atom …

Synthesis of spirocyclic pyrrolidines: Advanced building blocks for drug discovery

BA Chalyk, MV Butko, OO Yanshyna… - … A European Journal, 2017 - Wiley Online Library
In the context of drug discovery, novel spirocyclic pyrrolidines have been synthesized in two
steps from common three‐to seven‐membered‐ring (hetero) alicyclic ketones. The key …

1‐Substituted 2‐Azaspiro [3.3] heptanes: Overlooked Motifs for Drug Discovery

AA Kirichok, I Shton, M Kliachyna, I Pishel… - Angewandte …, 2017 - Wiley Online Library
The 2‐substituted piperidine core is found in drugs (18 FDA‐approved drugs), however,
their spirocyclic analogues remain unknown. Described here is the synthesis of spirocyclic …

Fluorine-containing prolines: Synthetic strategies, applications, and opportunities

PK Mykhailiuk - The Journal of Organic Chemistry, 2022 - ACS Publications
Fluorinated prolines play an important role in peptide studies, protein engineering,
medicinal chemistry, drug discovery, and agrochemistry. Since the first synthesis of 4 …

[HTML][HTML] Dynamical structure of the short multifunctional peptide BP100 in membranes

P Wadhwani, E Strandberg, J van den Berg… - … et Biophysica Acta (BBA …, 2014 - Elsevier
BP100 is a multifunctional membrane-active peptide of only 11 amino acids, with a high
antimicrobial activity, an efficient cell-penetrating ability, and low hemolytic side-effects. It …