CYP51 is an essential drug target for the treatment of primary amoebic meningoencephalitis (PAM)
Reaction mechanism of the methylation of a carboxylic acid R-COOH with... | Download Scientific Diagram
Absence of N-terminal acetyltransferase diversification during evolution of eukaryotic organisms | Scientific Reports
Molecules | Free Full-Text | Synthesis of MAPA Reagents and 2-Alkyl(aryl)aminopyridines from 2-Bromopyridine Using the Goldberg Reaction | HTML
Synthetic Approaches toward Monocyclic 3-Amino-β-lactams. - Abstract - Europe PMC
Metal‐Free Oxidative CC Bond Formation through CH Bond Functionalization - Narayan - 2015 - Chemistry – A European Journal - Wiley Online Library
Possible reaction mechanism of the hydrolysis of S -formylglutathione... | Download Scientific Diagram
Biosynthesis of UDP-L-Ara4N and transfer of the L-Ara4N unit to lipid... | Download Scientific Diagram
Direct Access to 4-Substituted Isoquinolones via a Sequential Pd-Catalyzed Cyclization/Base-Promoted Aromatization/Ring-Opening of N-Propargyl-1,3-oxazolidines - ScienceDirect
C-Glycopyranosyl Arenes and Hetarenes: Synthetic Methods and Bioactivity Focused on Antidiabetic Potential | Chemical Reviews
Control of protein life‐span by N‐terminal methionine excision | The EMBO Journal
Scheme 1. (a) MMTrCl/Py; (b) TMSCl/Py; (c) BzCl or Ac 2 O or (ClCH 2... | Download Scientific Diagram
N-terminomics identifies Prli42 as a membrane miniprotein conserved in Firmicutes and critical for stressosome activation in Listeria monocytogenes | Nature Microbiology
Transition Metal Catalyzed Enantioselective C(sp2)–H Bond Functionalization | ACS Catalysis
The deoxydehydration (DODH) reaction: a versatile technology for accessing olefins from bio-based polyols - Green Chemistry (RSC Publishing) DOI:10.1039/D0GC00689K
Control of protein life‐span by N‐terminal methionine excision | The EMBO Journal
The deoxydehydration (DODH) reaction: a versatile technology for accessing olefins from bio-based polyols - Green Chemistry (RSC Publishing) DOI:10.1039/D0GC00689K
Molecules | Free Full-Text | Synthesis of MAPA Reagents and 2-Alkyl(aryl)aminopyridines from 2-Bromopyridine Using the Goldberg Reaction | HTML
Rescuing the Last-Line Polymyxins: Achievements and Challenges | Pharmacological Reviews
Formation of naphthalene hydrates in the enzymatic conversion of 1,2-dihydronaphthalene by two fungal peroxygenases and subsequent naphthalene formation - ScienceDirect
Facile retro-Dieckmann cleavage of a pink phyllobilin: new type of potential downstream steps of natural chlorophyll breakdown | SpringerLink
Mobilization of a Kluyvera-like arnBCADTEF operon, besides mcr genes, confers colistin resistance to Escherichia coli isolated from healthy animals | bioRxiv
Direct Access to 4-Substituted Isoquinolones via a Sequential Pd-Catalyzed Cyclization/Base-Promoted Aromatization/Ring-Opening of N-Propargyl-1,3-oxazolidines - ScienceDirect
Metabolite damage and its repair or pre-emption | Nature Chemical Biology
Frontiers | Structural Basis of the Subcellular Topology Landscape of Escherichia coli | Microbiology
Biosynthesis of UDP-L-Ara4N and transfer of the L-Ara4N unit to lipid... | Download Scientific Diagram
Rescuing the Last-Line Polymyxins: Achievements and Challenges. - Abstract - Europe PMC
ARKAT USA, Inc. - ARKIVOC Monthly Newsletter (January 31, 2012)
![Thiazolo[5,4- d ]thiazoles – promising building blocks in the synthesis of semiconductors for plastic electronics - RSC Advances (RSC Publishing) DOI:10.1039/C3RA40851E](https://pubs.rsc.org/image/article/2013/RA/c3ra40851e/c3ra40851e-s4.gif "Thiazolo[5,4- d ]thiazoles – promising building blocks in the synthesis of semiconductors for plastic electronics - RSC Advances (RSC Publishing) DOI:10.1039/C3RA40851E")
Thiazolo[5,4- d ]thiazoles – promising building blocks in the synthesis of semiconductors for plastic electronics - RSC Advances (RSC Publishing) DOI:10.1039/C3RA40851E
