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Selective reduction of ox bile acids: synthesis of 3×,7p, and 12phydroxy bile acids Ashok K. Batty, The Surest K. Aggarwal, Gerald Sale, and Sarah Sheer Department of Medicine and the Sammy Davis,
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Selective reduction of oxo is a chemical process that involves converting an oxo group (a functional group consisting of an oxygen atom linked to a carbon atom by a double bond) into a hydroxyl group (functional group consisting of an oxygen atom linked to a hydrogen atom). This reduction reaction is often used in organic synthesis.
Selective reduction of oxo is typically performed by chemists, researchers, and individuals working in the field of organic chemistry. It may be required in various industries where selective reduction of oxo is a necessary step in the production of specific compounds or materials.
The process of filling out a selective reduction of oxo involves following a specific set of experimental procedures and reaction conditions. It requires knowledge of organic chemistry techniques and the appropriate selection of reducing agents and reaction conditions. Detailed protocols and instructions can be found in scientific literature or provided by experts in the field.
The purpose of selective reduction of oxo is to convert an oxo group into a hydroxyl group, enabling the synthesis of specific compounds or materials with desired properties. It is often utilized to transform aldehydes and ketones into their corresponding alcohols, which can have different applications in various industries, including pharmaceuticals, materials science, and manufacturing.
The information that must be reported on selective reduction of oxo depends on the specific context and requirements of the experiment or process. It typically includes details such as the starting material (aldehyde or ketone), the reducing agent used, reaction conditions (temperature, pressure, solvent, catalysts), specific yields or conversion rates, and any additional observations or characterization of the product formed.
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