Expanding the synthetic toolbox through metal–enzyme cascade reactions
S González-Granda, J Albarrán-Velo… - Chemical …, 2023 - ACS Publications
The combination of metal-, photo-, enzyme-, and/or organocatalysis provides multiple
synthetic solutions, especially when the creation of chiral centers is involved. Historically …
synthetic solutions, especially when the creation of chiral centers is involved. Historically …
Biaryl synthesis with arenediazonium salts: cross-coupling, CH-arylation and annulation reactions
FX Felpin, S Sengupta - Chemical Society Reviews, 2019 - pubs.rsc.org
The rich legacy of arenediazonium salts in the synthesis of unsymmetrical biaryls, built
around the seminal works of Pschorr, Gomberg and Bachmann more than a century ago …
around the seminal works of Pschorr, Gomberg and Bachmann more than a century ago …
Data science enables the development of a new class of chiral phosphoric acid catalysts
JP Liles, C Rouget-Virbel, JLH Wahlman, R Rahimoff… - Chem, 2023 - cell.com
The widespread success of BINOL-chiral phosphoric acids (CPAs) has led to the
development of several high molecular weight, sterically encumbered variants. Herein, we …
development of several high molecular weight, sterically encumbered variants. Herein, we …
Engineering enzymes for noncanonical amino acid synthesis
The standard proteinogenic amino acids grant access to a myriad of chemistries that
harmonize to create life. Outside of these twenty canonical protein building blocks are …
harmonize to create life. Outside of these twenty canonical protein building blocks are …
Reprogramming natural proteins using unnatural amino acids
A Adhikari, BR Bhattarai, A Aryal, N Thapa, KC Puja… - RSC …, 2021 - pubs.rsc.org
Unnatural amino acids have gained significant attention in protein engineering and drug
discovery as they allow the evolution of proteins with enhanced stability and activity. The …
discovery as they allow the evolution of proteins with enhanced stability and activity. The …
Aryl fluorosulfates: powerful and versatile partners in cross-coupling reactions
SK Saraswat, R Seemaladinne, H Zaini, N Ahmad… - RSC …, 2023 - pubs.rsc.org
Aryl fluorosulfates are versatile building blocks in organic synthesis and have gained
increasing attention in SuFEx (Sulfur Fluoride Exchange) click chemistry. They are easily …
increasing attention in SuFEx (Sulfur Fluoride Exchange) click chemistry. They are easily …
Synthesis of CBD and its derivatives bearing various C4′-side chains with a late-stage diversification method
X Gong, C Sun, MA Abame, W Shi, Y Xie… - The Journal of …, 2019 - ACS Publications
A novel synthetic route for making (−)-CBD and its derivatives bearing various C4′-side
chains is developed by a late-stage diversification method. Starting from commercially …
chains is developed by a late-stage diversification method. Starting from commercially …
Transition metal-catalyzed cross-coupling methodologies for the engineering of small molecules with applications in organic electronics and photovoltaics
Cross-coupling reactions have played a key role in producing numerous types of π-
conjugated small molecules having appealing properties for practical applications in organic …
conjugated small molecules having appealing properties for practical applications in organic …
Improved Synthesis of 4-Cyanotryptophan and Other Tryptophan Analogues in Aqueous Solvent Using Variants of TrpB from Thermotoga maritima
The use of enzymes has become increasingly widespread in synthesis as chemists strive to
reduce their reliance on organic solvents in favor of more environmentally benign aqueous …
reduce their reliance on organic solvents in favor of more environmentally benign aqueous …
New TRPM8 blockers exert anticancer activity over castration-resistant prostate cancer models
V Di Sarno, P Giovannelli, A Medina-Peris… - European Journal of …, 2022 - Elsevier
TRPM8 has recently emerged as a druggable target in prostate cancer (PC) and TRPM8
modulators have been proposed as potential anticancer agents in this pathology. We have …
modulators have been proposed as potential anticancer agents in this pathology. We have …