Access to N−CF3 Formamides by Reduction of N−CF3 Carbamoyl Fluorides

FG Zivkovic, C D.‐T. Nielsen… - Angewandte …, 2022 - Wiley Online Library
The departure into unknown chemical space is essential for the discovery of new properties
and function. We herein report the first synthetic access to N‐trifluoromethylated formamides …

Neurochemical regulators of food behavior for pharmacological treatment of obesity: current status and future prospects

GS Vardanyan, HS Harutyunyan… - Future Medicinal …, 2020 - Taylor & Francis
In recent decades, obesity has become a pandemic disease and appears to be an ultimate
medical and social problem. Existing antiobesity drugs show low efficiency and a wide …

The Alkyne Zipper Reaction: A Useful Tool in Synthetic Chemistry

ÅM Sørskår, HØK Stenstrøm, Y Stenstrøm… - Reactions, 2022 - mdpi.com
The alkyne zipper reaction is an internal-to-terminal alkyne isomerization reaction with many
interesting applications in synthetic chemistry, as it constitutes an efficient means of …

Coupling of sterically demanding peptides by β-thiolactone-mediated native chemical ligation

H Chen, Y Xiao, N Yuan, J Weng, P Gao… - Chemical …, 2018 - pubs.rsc.org
The ligation of sterically demanding peptidyl sites such as those involving Val–Val and Val–
Pro linkages has proven to be extremely challenging with conventional NCL methods that …

Design, synthesis and biological evaluation of new 1, ω-Bis-(5-alkyl-3-tosyl-1, 3, 4, 2-triazaphospholino) alkanes as in vitro α-amylase and lipase inhibitors

S Hamzaoui, BB Salah, S Bouguerra, K Hamden… - International Journal of …, 2023 - Elsevier
A series of new 1, ω-bis-(5-alkyl-3-tosyl-1, 3, 4, 2-triazaphospholino) alkanes 2 and 3 were
obtained in excellent yields by the condensation of 1, ω-bis-(1-tosylamidrazone) alkanes 1 …

Stereochemical structure activity relationship studies (S-SAR) of tetrahydrolipstatin

X Liu, Y Wang, RI Duclos Jr… - ACS Medicinal Chemistry …, 2018 - ACS Publications
Tetrahydrolipstatin (THL), its enantiomer, and an additional six diastereomers were
evaluated as inhibitors of the hydrolysis of p-nitrophenyl butyrate by porcine pancreatic …

De Novo Asymmetric Synthesis of Avocadyne, Avocadene, and Avocadane Stereoisomers

VLS Cunha, X Liu, TL Lowary… - The Journal of Organic …, 2019 - ACS Publications
The de novo asymmetric synthesis of all possible stereoisomers of two polyketide natural
products, avocadyne, avocadene, and the saturated variant avocadane, is described. The …

[HTML][HTML] Exploration of the Fusidic Acid Structure Activity Space for Antibiotic Activity

YS Kang, SC Silva, K Smith, K Sumida, Y Wang… - Molecules, 2025 - mdpi.com
Fusidic acid is a translation inhibitor with activity against major Gram-positive bacterial
pathogens such as S. aureus. However, its activity against Gram-negatives is poor based on …

De Novo Asymmetric Approach to Aspergillide‐C: Synthesis of 4‐epi‐seco‐Aspergillide‐C

Y Xing, GA O'Doherty - ChemistrySelect, 2022 - Wiley Online Library
An asymmetric approach toward the synthesis of the marine natural product aspergillide‐C
has been developed. The convergent asymmetric synthesis uses two asymmetric Noyori …

Total Synthesis of Tetrahydrolipstatin, Its Derivatives, and Evaluation of Their Ability to Potentiate Multiple Antibiotic Classes against Mycobacterium Species

SS Khan, TD Sudasinghe, AD Landgraf… - ACS infectious …, 2021 - ACS Publications
Tetrahydrolipstatin (THL, 1a) has been shown to inhibit both mammalian and bacterial α/β
hydrolases. In the case of bacterial systems, THL is a known inhibitor of several …