Results 61 to 70 of about 3,332 (181)

Revisit to ()-Civetone Synthesis

open access: yesNatural Product Communications, 2012
The synthesis of ( Z )-civetone ( 1 ) is described starting from oleic acid ( 5 ) via a series of reactions, intermolecular olefin self-metathesis, bromination/dehydrobromination into acetylene, semi-hydrogenation and intramolecular Dieckmann ...
Hisahiro Hagiwara   +4 more
doaj   +1 more source

Characterization of a dual function macrocyclase enables design and use of efficient macrocyclization substrates

open access: yesNature Communications, 2017
Cyclic peptide macrocycles are promising anti-cancer and antimicrobial molecules. Here, the authors characterize the structure and catalytic mechanism of the prolyl oligopeptidase B from Basidiomycete fungi, showing that its dual macrocyclase-peptidase ...
Clarissa M. Czekster   +3 more
doaj   +1 more source

Dynamic Supramolecular Polyurethane Elastomers Enabling Bioinspired Strain‐Adaptive Stiffening to Resolve the Softness–Strength Paradox

open access: yesAdvanced Science, Volume 13, Issue 31, 4 June 2026.
Segmental‐level molecular engineering of a supramolecular polyurethane elastomer integrates strain‐adaptive chains, soft elastic segments, and dynamic hydrogen bonding motifs. This design reconciles skin‐like softness with muscle‐level strength, offering a sustainable and high‐performance material platform for next‐generation artificial skin and soft ...
Haoming Zou   +5 more
wiley   +1 more source

macrocycle

open access: yes, 2014
Citation: 'macrocycle' in the IUPAC Compendium of Chemical Terminology, 3rd ed.; International Union of Pure and Applied Chemistry; 2006. Online version 3.0.1, 2019. 10.1351/goldbook.M03662 • License: The IUPAC Gold Book is licensed under Creative Commons Attribution-ShareAlike CC BY-SA 4.0 International for individual terms.
openaire   +2 more sources

Synthesis of Monothiacalix[4]arene Using the Fragment Condensation Approach

open access: yesMolecules
The article describes a simple and scalable preparation of 2-monothiacalix[4]arene 7, the simplest representative of the mixed-bridged (CH2 and S) calix[4]arenes.
Daniel Kortus   +7 more
doaj   +1 more source

Access to Macrocycles with an endo Aryl Ether and an endo Aryl-Aryl Bond, Development and Application

open access: yesCHIMIA, 2011
Macrocyclization methodologies allowing access to macrocycles having an endo aryl ether and an endo aryl–aryl bond, especially those based on an intramolecular SNAr reaction and the Suzuki-Miyaura reaction, are summarized.
Qian Wang, Jieping Zhu
doaj   +1 more source

A Short Synthesis of Cyclo(‐RGDfK) Using a Microflow Reactor

open access: yesChemistryEurope, Volume 4, Issue 6, June 2026.
An efficient synthesis of cyclo(‐RGDfK) was achieved by combining a one‐flow three‐component coupling (3CC) reaction via α‐amino acid N‐carboxy anhydrides with rapid macrolactamization using a microflow reactor. Precise control of the water content and base loading in the 3CC reaction enabled the gram‐scale synthesis of the desired tripeptides and ...
Naoto Yamasaki   +6 more
wiley   +1 more source

Direct and indirect single electron transfer (SET)-photochemical approaches for the preparation of novel phthalimide and naphthalimide-based lariat-type crown ethers

open access: yesBeilstein Journal of Organic Chemistry, 2014
In this review, we describe direct and indirect photochemical approaches that have been developed for the preparation of phthalimide- and naphthalimide-based, lariat-type crown ethers.
Dae Won Cho   +2 more
doaj   +1 more source

Case Studies of the Synthesis of Bioactive Cyclodepsipeptide Natural Products

open access: yesMolecules, 2013
Cyclodepsipeptide natural products often display intriguing biological activities that along with their complex molecular scaffolds, makes them interesting targets for chemical synthesis.
Markus Kaiser, Sara C. Stolze
doaj   +1 more source

Macrocycles

open access: yesDrug Discovery Today: Technologies, 2018
Macrocycles are an emerging and largely underexploited part of chemical space where potential drugs for difficult genomic targets can be discovered. Macrocycles can have advantages over their natural twins such as better control over synthesis, physicochemical properties and target binding.
Abdelraheem, Eman M.M.   +2 more
openaire   +1 more source

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