Facile Reduction of Carboxylic Acids to Primary Alcohols under Metal-free and Solvent-free Conditions
Panda, Tarun K and Harinath, A and Bhattacharjee, J (2018) Facile Reduction of Carboxylic Acids to Primary Alcohols under Metal-free and Solvent-free Conditions. Chemical Communications. ISSN 1359-7345
Text
Chemical Communications_1-4_2018.pdf - Accepted Version Restricted to Repository staff only until November 2019. Download (2MB) | Request a copy |
Abstract
We report the development of a facile protocol for the deoxygenative hydroboration of aliphatic and aryl carboxylic acids to afford corresponding primary alcohols under solvent-free and catalyst-free conditions. The reaction proceeds under ambient temperature exhibits good tolerance towards various functional groups and generates quantitative yields. The plausible mechanism involves the formation of Lewis acid–base adducts as well as the liberation of hydrogen gas.
IITH Creators: |
|
||||
---|---|---|---|---|---|
Item Type: | Article | ||||
Subjects: | Chemistry | ||||
Divisions: | Department of Chemistry | ||||
Depositing User: | Team Library | ||||
Date Deposited: | 03 Jan 2019 09:53 | ||||
Last Modified: | 17 Jan 2019 03:43 | ||||
URI: | http://raiithold.iith.ac.in/id/eprint/4652 | ||||
Publisher URL: | http://doi.org/10.1039/C8CC08841A | ||||
OA policy: | http://www.sherpa.ac.uk/romeo/issn/1359-7345/ | ||||
Related URLs: |
Actions (login required)
View Item |
Statistics for this ePrint Item |
Altmetric