![Photo-on-Demand Base-Catalyzed Phosgenation Reactions with Chloroform: Synthesis of Arylcarbonate and Halocarbonate Esters | The Journal of Organic Chemistry Photo-on-Demand Base-Catalyzed Phosgenation Reactions with Chloroform: Synthesis of Arylcarbonate and Halocarbonate Esters | The Journal of Organic Chemistry](https://pubs.acs.org/cms/10.1021/acs.joc.1c01210/asset/images/medium/jo1c01210_0002.gif)
Photo-on-Demand Base-Catalyzed Phosgenation Reactions with Chloroform: Synthesis of Arylcarbonate and Halocarbonate Esters | The Journal of Organic Chemistry
![How can you convert a carboxylic acid into an ester? a. Heat with an alcohol and catalytic acid. b. Deprotonate with a base and react with an alcohol. c. Deprotonate with a How can you convert a carboxylic acid into an ester? a. Heat with an alcohol and catalytic acid. b. Deprotonate with a base and react with an alcohol. c. Deprotonate with a](https://homework.study.com/cimages/multimages/16/ester_synthesis2568131255495951183.png)
How can you convert a carboxylic acid into an ester? a. Heat with an alcohol and catalytic acid. b. Deprotonate with a base and react with an alcohol. c. Deprotonate with a
![Organocatalytic Lewis base functionalisation of carboxylic acids, esters and anhydrides via C1-ammonium or azolium enolates - Chemical Society Reviews (RSC Publishing) DOI:10.1039/C4CS00042K Organocatalytic Lewis base functionalisation of carboxylic acids, esters and anhydrides via C1-ammonium or azolium enolates - Chemical Society Reviews (RSC Publishing) DOI:10.1039/C4CS00042K](https://pubs.rsc.org/image/article/2014/CS/c4cs00042k/c4cs00042k-f3_hi-res.gif)