Antibiotics | Free Full-Text | Investigating the OXA Variants of ESKAPE Pathogens
File:Oxa-di-p-methane rearrangement mechanism.png - Wikimedia Commons
OXA-23 - BIOCONNECTIONS
3-Oxa-9-aza-bicyclo[3.3.1]nonan-7-ol, 9-methyl-, benzillic acid ester, maleate (1 to 1)
RCSB PDB - 7KHY: Crystal structure of OXA-163 K73A in complex with meropenem
File:8-Oxa Cocaine Structure.svg - Wikipedia
File:7-Oxa-1,5-diaza-8-mercura-bicyclo(4.2.0)octan.svg - Wikimedia Commons
Oxa Group | Facebook
Antibiotics | Free Full-Text | OXA-48 Carbapenemase-Producing Enterobacterales in Spanish Hospitals: An Updated Comprehensive Review on a Rising Antimicrobial Resistance
![3aS,7aα)-8,8-Dimethyl-3aβ,6β-methanospiro[1-oxa -2-thia(IV)-hydrindane-2,2′-[1-oxa-2-thia(IV)-3]cyclopentene]-5′-one | Chemical Substance Information | J-GLOBAL](https://jglobal.jst.go.jp/images/chemical/detail/010/905/J1.090.561C.png "3aS,7aα)-8,8-Dimethyl-3aβ,6β-methanospiro[1-oxa -2-thia(IV)-hydrindane-2,2′-[1-oxa-2-thia(IV)-3]cyclopentene]-5′-one | Chemical Substance Information | J-GLOBAL")
3aS,7aα)-8,8-Dimethyl-3aβ,6β-methanospiro[1-oxa -2-thia(IV)-hydrindane-2,2′-[1-oxa-2-thia(IV)-3]cyclopentene]-5′-one | Chemical Substance Information | J-GLOBAL
Tutorial Examples
Stereoselective Syntheses of 4-Oxa Diaminopimelic Acid and Its Protected Derivatives via Aziridine Ring Opening | Organic Letters
Whole genome sequencing characterization of Slovenian carbapenem-resistant Klebsiella pneumoniae, including OXA-48 and NDM-1 producing outbreak isolates | PLOS ONE
Oxa - Name meaning, origin, variations and more
File:Oxa logo new.png - Wikimedia Commons
OXA-01 | mTORC Inhibitor | MedChemExpress
RCSB PDB - 5IY2: Structure of apo OXA-143 carbapenemase
OXA-LACTEAT - OXA - CYGYC - Chemical specialities
OXA - 4000 ESPECIAL - OXA - CYGYC - Chemical specialities
![Highly efficient construction of an oxa-[3.2.1]octane-embedded 5–7–6 tricyclic carbon skeleton and ring-opening of the bridged ring via C–O bond cleav ... - RSC Advances (RSC Publishing) DOI:10.1039/D2RA01315K](https://pubs.rsc.org/image/article/2022/RA/d2ra01315k/d2ra01315k-s4_hi-res.gif "Highly efficient construction of an oxa-[3.2.1]octane-embedded 5–7–6 tricyclic carbon skeleton and ring-opening of the bridged ring via C–O bond cleav ... - RSC Advances (RSC Publishing) DOI:10.1039/D2RA01315K")
Highly efficient construction of an oxa-[3.2.1]octane-embedded 5–7–6 tricyclic carbon skeleton and ring-opening of the bridged ring via C–O bond cleav ... - RSC Advances (RSC Publishing) DOI:10.1039/D2RA01315K
