The reduction of ketones to alcohols is a common reaction learned in organic chemistry. Traditional methods of ketone reduction, while effective, lead to inefficient use of energy and resources. The purpose of this research was to introduce green chemistry techniques to the reaction of ketones with sodium borohydride. Microwave irradiation was used in place of the traditional refluxing process, and silica gel was used as a solid support instead of solvent. Eight different cyclohexanones variable substitution patterns were reduced using this method. The parameters of time and solid support amounts were optimized to between 2–5 minutes depending on the starting ketone, and a ratio of 2:4 sodium borohydride: solid support. These reduced keton...
For developing the teaching materials of green chemistry at the students' laboratories in secondary ...
Secondary and tertiary alcohols synthesized via allylation of aldehydes and ketones are important co...
Sodium borohydride (0.4–1.5 equivalents) in the presence of ammonium oxalate (0.2 equivalents) reduc...
[[sponsorship]]基因體研究中心[[note]]已出版;[SCI];有審查制度;具代表性[[note]]http://gateway.isiknowledge.com/gateway/Ga...
Reduction of keto esters is a valuable alternative to produce diols. Sodium borohydride/MeOH system ...
This experiment aims to reduce the aromatic benzophenone to diphenylmethanol (Benhydrol). Sodium bor...
The combination of sodium borohydride and amberlyst-15 (H+) in tetrahydrofurane is a powerful reduct...
Chemoselective reductions are valuable in organic synthesis and are routinely discussed in a sophomo...
The purpose of this research is to develop an organic chemistry lab that compares methods of charact...
Several ketones and aldehydes were hydrogenated with Frustrated Lewis pair (FLP) conditions using mi...
Formerly, our lab developed a one-pot synthesis for the reductive alkylation of monosubstituted malo...
Secondary alcohols are oxidized to corresponding ketones. Both aromatic and aliphatic secondary alco...
The project of this thesis is the comparative study of sodium borohydride catalyzed reactions ...
Green chemistry is a method of designing, manufacturing, and using chemical compounds that actively ...
Reduction of structurally different carbonyl compounds such as aldehydes, ketones, alpha,beta-unsatu...
For developing the teaching materials of green chemistry at the students' laboratories in secondary ...
Secondary and tertiary alcohols synthesized via allylation of aldehydes and ketones are important co...
Sodium borohydride (0.4–1.5 equivalents) in the presence of ammonium oxalate (0.2 equivalents) reduc...
[[sponsorship]]基因體研究中心[[note]]已出版;[SCI];有審查制度;具代表性[[note]]http://gateway.isiknowledge.com/gateway/Ga...
Reduction of keto esters is a valuable alternative to produce diols. Sodium borohydride/MeOH system ...
This experiment aims to reduce the aromatic benzophenone to diphenylmethanol (Benhydrol). Sodium bor...
The combination of sodium borohydride and amberlyst-15 (H+) in tetrahydrofurane is a powerful reduct...
Chemoselective reductions are valuable in organic synthesis and are routinely discussed in a sophomo...
The purpose of this research is to develop an organic chemistry lab that compares methods of charact...
Several ketones and aldehydes were hydrogenated with Frustrated Lewis pair (FLP) conditions using mi...
Formerly, our lab developed a one-pot synthesis for the reductive alkylation of monosubstituted malo...
Secondary alcohols are oxidized to corresponding ketones. Both aromatic and aliphatic secondary alco...
The project of this thesis is the comparative study of sodium borohydride catalyzed reactions ...
Green chemistry is a method of designing, manufacturing, and using chemical compounds that actively ...
Reduction of structurally different carbonyl compounds such as aldehydes, ketones, alpha,beta-unsatu...
For developing the teaching materials of green chemistry at the students' laboratories in secondary ...
Secondary and tertiary alcohols synthesized via allylation of aldehydes and ketones are important co...
Sodium borohydride (0.4–1.5 equivalents) in the presence of ammonium oxalate (0.2 equivalents) reduc...