Sign Up to like & get
recommendations!
1
Published in 2022 at "Organic letters"
DOI: 10.1021/acs.orglett.2c02027
Abstract: Herein, we describe a method to produce (Z)-trifluoromethyl enol esters via the olefination and trifluoromethylation of carboxylic acids with TMSCF3. This synthetic method uses inexpensive and easy-to-handle TMSCF3. It employs a commercially available CuCl catalyst…
read more here.
Keywords:
olefination trifluoromethylation;
enol esters;
trifluoromethyl enol;
carboxylic acids ... See more keywords
Sign Up to like & get
recommendations!
1
Published in 2022 at "Organic letters"
DOI: 10.1021/acs.orglett.2c02860
Abstract: In the presence of TiCl3, the reductive cyclization of tetrasubstituted enol esters bearing a 2-(ortho-nitroaryl) substituent affords 3-acyloxy-2,3-disubstituted indolenines in good yields. A domino process involving the partial reduction of nitro to a nitroso group…
read more here.
Keywords:
reductive cyclization;
acyloxyindolenines ticl3;
synthesis acyloxyindolenines;
ortho nitroaryl ... See more keywords
Sign Up to like & get
recommendations!
0
Published in 2020 at "ACS Omega"
DOI: 10.1021/acsomega.9b03936
Abstract: A combination of ruthenium catalyst with silver salt and copper salt was proved to be a highly efficient protocol for the direct addition reaction of benzoic acids with unsymmetrical trifluoromethylated internal alkynes. Diverse trifluoromethyl group-substituted…
read more here.
Keywords:
group substituted;
addition;
trifluoromethyl group;
substituted enol ... See more keywords
Sign Up to like & get
recommendations!
0
Published in 2018 at "Organic chemistry frontiers"
DOI: 10.1039/c8qo00664d
Abstract: An efficient Cu(I)-catalyzed stereoselective synthesis of trisubstituted Z-enol esters via interrupting the 1,3-O-transposition process is reported. This method provided a convenient approach to highly functionalized Z-enol esters with mild reaction conditions and wide substrate scope.
read more here.
Keywords:
trisubstituted enol;
esters via;
stereoselective synthesis;
catalyzed stereoselective ... See more keywords
Sign Up to like & get
recommendations!
2
Published in 2023 at "Chemical Science"
DOI: 10.1039/d3sc01394d
Abstract: Carboacyloxylation of internal alkynes is emerging as a powerful and straightforward strategy for enol ester synthesis. However, the reported examples come with limitations, including the utilization of noble metal catalysts, the control of regio- and…
read more here.
Keywords:
synthesis;
enol;
lewis acid;
enol esters ... See more keywords