Recent advances in bioorthogonal click chemistry for biomedical applications

A Battigelli, B Almeida, A Shukla - Bioconjugate Chemistry, 2022 - ACS Publications
Bioorthogonal click chemistry, first introduced in the early 2000s, has become one of the
most widely used approaches for designing advanced biomaterials for applications in tissue …

An expeditious route to sterically encumbered nonproteinogenic α-amino acid precursors using allylboronic acids

S Sahu, G Karan, L Roy, MS Maji - Chemical Science, 2022 - pubs.rsc.org
A diastereoselective allylation of N-tert-butane sulfinyl α-iminoesters using allylboronic acids
is developed to obtain optically active non-proteinogenic α-amino acid precursors in good …

Photo-cleavable purification/protection handle assisted synthesis of giant modified proteins with tandem repeats

X Liu, J Liu, Z Wu, L Chen, S Wang, P Wang - Chemical Science, 2019 - pubs.rsc.org
Proteins with tandem repeats have essential physical or biological roles in cells and have
been widely investigated as biomaterials or vaccines. Chemically derived proteins with …

Facile synthesis of vinyl sulfoxides via external oxidant-free oxidative condensation of phenylglycinols with DMSO

X Shi, R Zhang, C Liu, Z Zuo, H Feng - Tetrahedron Letters, 2024 - Elsevier
Oxidative activation of Csingle bondO, Csingle bondN and Csingle bondC bonds has
recently emerged as a powerful method for the synthesis of valuable organic compounds …

4, 5-Dioxo-imidazolinium Cation Activation of 1-Acyl-1-carbamoyl Oximes: Access to Cyanoformamides Using Dichloroimidazolidinedione

Y Gao, Z Zhang, Z Li, T Guo, Y Zhu, Z Yao… - The Journal of …, 2019 - ACS Publications
Cyanoformamides are prevalent as versatile building blocks for accessing synthetically
useful intermediates and biologically active compounds. The development of a milder …

A novel route for the synthesis of androgen receptor antagonist enzalutamide

X Meng, S Bi, S Jin, K Wu, S Wu, L Shao… - Chinese Chemical …, 2023 - Elsevier
A novel route of enzalutamide was developed in five steps. Starting from 4-amino-2-
(trifluoromethyl) benzonitrile (7) and Boc-2-aminoisobutyric acid (16), condensation …

One-pot oxime ligation from peptides bearing thiazolidine and aminooxyacetyl groups

S Duflocq, J Zhou, F Huguenot, M Vidal, WQ Liu - RSC advances, 2020 - pubs.rsc.org
One-pot oxime ligation under mild conditions using Pd (II) as a shared catalyst from an
aldehyde precursor (Thz) and a protected aminooxyacetyl group (Proc-Aoa) is reported. Two …

Cu (II)/THPTA-Mediated Thiazolidine Deprotection for Living Phages and Cell Surfaces Labeling

C Ma, G Liu, J Sun, D Luo, J Yin, D Yang, S Pang… - 2024 - chemrxiv.org
Incorporating unnatural bioorthogonal groups into peptides and proteins offers an excellent
opportunity to endow them with new properties in a precise and controlled manner. Among …