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A REVIEW ON SYNTHESIS AND PHARMACOLOGICAL DIVERSITY OF ISOXAZOLES & PYRAZOLINES | NUJPS
Reductive ring scission reactions of the 1,2-benzisoxazole-containing... | Download Scientific Diagram
An overview of metal-free synthetic routes to isoxazoles: the privileged scaffold - RSC Advances (RSC Publishing) DOI:10.1039/D1RA04624A
Elucidation of a Novel Bioactivation Pathway of a 3,4-Unsubstituted Isoxazole in Human Liver Microsomes: Formation of a Glutathione Adduct of a Cyanoacrolein Derivative after Isoxazole Ring Opening | Drug Metabolism & Disposition
Clean and efficient synthesis of isoxazole derivatives in aqueous media. - Abstract - Europe PMC
Ring-Opening Fluorination of Isoxazoles | Organic Letters
View of ISOXAZOLE–A POTENT PHARMACOPHORE | International Journal of Pharmacy and Pharmaceutical Sciences
The synthetic and therapeutic expedition of isoxazole and its analogs | SpringerLink
Isoxazole Ring - an overview | ScienceDirect Topics
Fig. 2. | Reductive Isoxazole Ring Opening of the Anticoagulant Razaxaban Is the Major Metabolic Clearance Pathway in Rats and Dogs | Drug Metabolism & Disposition
Proposed mechanisms for the metabolic isoxazole ring opening in the... | Download Scientific Diagram
Proposed mechanisms for the metabolic isoxazole ring opening in the... | Download Scientific Diagram
The synthetic and therapeutic expedition of isoxazole and its analogs | SpringerLink
View of ISOXAZOLE–A POTENT PHARMACOPHORE | International Journal of Pharmacy and Pharmaceutical Sciences
An overview of metal-free synthetic routes to isoxazoles: the privileged scaffold - RSC Advances (RSC Publishing) DOI:10.1039/D1RA04624A
Elucidation of a Novel Bioactivation Pathway of a 3,4-Unsubstituted Isoxazole in Human Liver Microsomes: Formation of a Glutathione Adduct of a Cyanoacrolein Derivative after Isoxazole Ring Opening | Drug Metabolism & Disposition
Ring-Opening Fluorination of Isoxazoles | Organic Letters
Isoxazole Ring - an overview | ScienceDirect Topics
synthesis of isoxazoles - YouTube
Host-Catalyzed Isoxazole Ring Opening: A Rationally Designed Artificial Enzyme | Journal of the American Chemical Society