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

и другие.

Science Advances, Год журнала: 2024, Номер 10(38)

Опубликована: Сен. 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.

Язык: Английский

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

Alberto Fidi

и другие.

Langmuir, Год журнала: 2024, Номер 40(24), С. 12381 - 12393

Опубликована: Июнь 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.

Язык: Английский

Процитировано

1

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

Small, Год журнала: 2024, Номер 20(42)

Опубликована: Июль 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.

Язык: Английский

Процитировано

1

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

и другие.

New Journal of Chemistry, Год журнала: 2024, Номер 48(30), С. 13654 - 13658

Опубликована: Янв. 1, 2024

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

Язык: Английский

Процитировано

1

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

Dou Zhang,

Yajing Chang

и другие.

Organic Chemistry Frontiers, Год журнала: 2024, Номер 11(19), С. 5422 - 5428

Опубликована: Янв. 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.

Язык: Английский

Процитировано

1

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

и другие.

Science Advances, Год журнала: 2024, Номер 10(38)

Опубликована: Сен. 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.

Язык: Английский

Процитировано

1