β-Silyl alkynoates: Versatile reagents for biocompatible and selective amide bond formation DOI Creative Commons
Khokan Choudhuri, Zhenguo Zhang, Teck‐Peng Loh

et al.

Science Advances, Journal Year: 2024, Volume and Issue: 10(38)

Published: Sept. 18, 2024

The study introduces a previously unidentified method for amide bond formation that addresses several limitations of conventional approaches. It uses the β-silyl alkynoate molecule, where alkynyl group activates ester efficient formation, while bulky TIPS (triisopropylsilane) prevents unwanted 1,4-addition reactions. This approach exhibits high chemoselectivity amines, making compatible with wide range substrates, including secondary and targets specific ε-amino lysine among native amino ester’s derivatives. maintains stereochemistry during removal, allowing versatile platform postsynthesis modifications such as click reactions peptide-drug conjugations. These advancements hold substantial promise pharmaceutical development peptide engineering, opening avenues research applications.

Language: Английский

A Promising Compound for Green Multiresponsive Materials Based on Acyl Carrier Protein DOI
Mert Acar, Duccio Tatini,

Alberto Fidi

et al.

Langmuir, Journal Year: 2024, Volume and Issue: 40(24), P. 12381 - 12393

Published: June 5, 2024

A gel that exhibits intrinsically multiple-responsive behavior was prepared from an oligopeptide and studied. ACP(65-74) is active decapeptide fragment of acyl carrier protein. We investigated 3% w/v ACP(65-74)-NH2 self-healing physical gels in water, glycerol carbonate (GC), their mixtures. The morphology by optical, birefringence, confocal laser scanning microscopy, circular dichroism, Fourier transform infrared, fluorescence spectroscopy experiments. found all samples possess pH responsiveness with fully reversible sol-to-gel transitions. rheological properties depend on the temperature solvent composition. dependence water shows a peculiar similar to thermoresponsive polymer solutions. results reveal presence several β-sheet structures amyloid aggregates, offering valuable insights into fibrillation mechanism amyloids different media.

Language: Английский

Citations

1

Multi‐Colored Aqueous Ink for Rewritable Paper DOI
Nikita Das, Chandan Maity

Small, Journal Year: 2024, Volume and Issue: 20(42)

Published: July 16, 2024

As sustainable and eco-friendly replacements to conventional paper, rewritable paper is a very attractive alternative for communication, information circulation, storage. Development made using chromogenic materials that change its color in presence of external stimuli. However, the new techniques have faced several major challenges including feasible operational method, approach. Herein, simple, convenient, strategy described preparation substrate, multi colored ink efficient use writing, painting or printing purpose. In addition, writing with "invisible ink" on can be realized potential anti-counterfeiting application. The written, painted, printed substrate easily erased an aqueous solution. Thus, original retrieved reused multiple times. Besides, written retained prolonged time at ambient conditions. Overall, this approach shows as prototype multicolor writing/painting application, offering solution reducing waste promoting environmental stewardship.

Language: Английский

Citations

1

Visible-light-induced Fe(iii)-promoted reduction amidation of 1,4,2-dioxazol-5-one DOI
Bosen Wang, Hao Li, Minmin Liu

et al.

New Journal of Chemistry, Journal Year: 2024, Volume and Issue: 48(30), P. 13654 - 13658

Published: Jan. 1, 2024

This method describes the iron-promoted amidation of dioxazolone under visible light to obtain aromatic/alkyl substituted amides.

Language: Английский

Citations

1

TFPN-mediated racemization/epimerization-free amide and peptide bond formation DOI
Jinhua Yang,

Dou Zhang,

Yajing Chang

et al.

Organic Chemistry Frontiers, Journal Year: 2024, Volume and Issue: 11(19), P. 5422 - 5428

Published: Jan. 1, 2024

A new electron-deficient aromatic-based coupling reagent, tetrafluorophthalonitrile (TFPN), designed according to the concept of dual reagents, is developed facilitate amide and peptide bond formation in a one-pot, two-step manner.

Language: Английский

Citations

1

β-Silyl alkynoates: Versatile reagents for biocompatible and selective amide bond formation DOI Creative Commons
Khokan Choudhuri, Zhenguo Zhang, Teck‐Peng Loh

et al.

Science Advances, Journal Year: 2024, Volume and Issue: 10(38)

Published: Sept. 18, 2024

The study introduces a previously unidentified method for amide bond formation that addresses several limitations of conventional approaches. It uses the β-silyl alkynoate molecule, where alkynyl group activates ester efficient formation, while bulky TIPS (triisopropylsilane) prevents unwanted 1,4-addition reactions. This approach exhibits high chemoselectivity amines, making compatible with wide range substrates, including secondary and targets specific ε-amino lysine among native amino ester’s derivatives. maintains stereochemistry during removal, allowing versatile platform postsynthesis modifications such as click reactions peptide-drug conjugations. These advancements hold substantial promise pharmaceutical development peptide engineering, opening avenues research applications.

Language: Английский

Citations

1