J Lou, Q Wang, P Wu, H Wang, YG Zhou… - Chemical Society …, 2020 - pubs.rsc.org
Carbon–sulfur bond cross-coupling has become more and more attractive as an alternative protocol to establish carbon–carbon and carbon–heteroatom bonds. Diverse …
KM Korch, DA Watson - Chemical reviews, 2019 - ACS Publications
At the advent of cross-coupling chemistry, carbon electrophiles based on halides or pseudohalides were the only suitable electrophilic coupling partners. Almost two decades …
GS Lee, SH Hong - Accounts of Chemical Research, 2023 - ACS Publications
Conspectus Synthetic chemists have consistently aimed to develop efficient methods for synthesizing ketones, which are essential building blocks in organic chemistry and play …
SI Ting, DW Snelson, TR Huffman… - Journal of the …, 2023 - ACS Publications
Small molecules that modulate the 14-3-3 protein–protein interaction (PPI) network represent valuable therapeutics and tool compounds. However, access has been lost to 14 …
S Yang, X Yu, M Szostak - ACS catalysis, 2023 - ACS Publications
Transition-metal-catalyzed cross-coupling reactions of thioesters by selective acyl C (O)–S cleavage have emerged as a powerful platform for the preparation of complex molecules …
F Buttard, J Sharma, PA Champagne - Chemical Communications, 2021 - pubs.rsc.org
Alkenes bearing four carbon-based groups are ubiquitous motifs in chemical sciences due to their various applications from medicinal to materials chemistry, and as chemical …
GS Lee, B Park, SH Hong - Nature Communications, 2022 - nature.com
The direct modification of naturally occurring chiral amino acids to their amino ketone analogs is a significant synthetic challenge. Here, an efficient and robust cross-coupling …
Isocyanides have long been known as versatile chemical reagents in organic synthesis. Their ambivalent nature also allows them to function as a CO-substitute in palladium …
YP Budiman, SA Westcott, U Radius… - Advanced Synthesis & …, 2021 - Wiley Online Library
Organoboron compounds are well known building blocks for many organic reactions. However, under basic conditions, polyfluorinated aryl boronic acid derivatives suffer from …