Oxidative rearrangement of 1, 1-disubstituted alkenes to ketones
The Wacker process, which is widely used to convert monosubstituted alkenes into the
corresponding methyl ketones, is thought to proceed through a PdII/Pd0 catalytic cycle …
corresponding methyl ketones, is thought to proceed through a PdII/Pd0 catalytic cycle …
Silica sulfuric acid and silica chloride as efficient reagents for organic reactions
Silica sulfuric acid and silica chloride, two silica based solid acids have been used for
various organic functional group transformations either as reagent or as catalyst. All …
various organic functional group transformations either as reagent or as catalyst. All …
Sustainable routes to alkenes: applications of homogeneous catalysis to the dehydration of alcohols to alkenes
DJ Ward, DJ Saccomando, G Walker… - Catalysis Science & …, 2023 - pubs.rsc.org
With the growing scientific and social awareness of environmental issues, there is an
increasing demand for renewable alkene feedstocks used to make the products we rely on …
increasing demand for renewable alkene feedstocks used to make the products we rely on …
Intramolecular Dehydration of Cyclic Alcohols to Cyclic Alkenes via Cation- and Anion-Confined Catalysis over Ionic Liquids
R Li, X Zhou, Z Li, Y Wang, Y Zhao, Z Liu… - ACS Sustainable …, 2023 - ACS Publications
Catalytic intramolecular dehydration of cyclic alcohols to cyclic alkenes is very interesting
but still challenging due to low selectivity and difficulty in separation. Herein, we report a …
but still challenging due to low selectivity and difficulty in separation. Herein, we report a …
An efficient synthetic route for quinazolinyl 4-thiazolidinones
JR Mali, UR Pratap, PD Netankar, RA Mane - Tetrahedron Letters, 2009 - Elsevier
An efficient solvent-free cyclocondensation route for condensing mercaptoacetic acid with
quinazolinyl-substituted azomethines has been developed using silica chloride as a catalyst …
quinazolinyl-substituted azomethines has been developed using silica chloride as a catalyst …
Flow chemistry enhances catalytic alcohol-to-alkene dehydration
Hf (OTf) 4 was identified as an excellent catalyst for the low temperature (180° C)
dehydration of 1-hexanol to hexenes and 2-methyl-1-butanol to 2-methylbutenes. Batch …
dehydration of 1-hexanol to hexenes and 2-methyl-1-butanol to 2-methylbutenes. Batch …
Amberlyst®-15: A reusable heterogeneous catalyst for the dehydration of tertiary alcohols
LMT Frija, CAM Afonso - Tetrahedron, 2012 - Elsevier
Tertiary alcohols react under mild conditions in the presence of Amberlyst®-15 (dry)(solid-
supported sulfonic acid) to give predominantly the most stable alkene in very good yield …
supported sulfonic acid) to give predominantly the most stable alkene in very good yield …
Triphosgene and DMAP as mild reagents for chemoselective dehydration of tertiary alcohols
The utility of triphosgene and DMAP as mild reagents for chemoselective dehydration of
tertiary alcohols is reported. Performed in dichloromethane at room temperature, this …
tertiary alcohols is reported. Performed in dichloromethane at room temperature, this …
[HTML][HTML] Synthesis of 2, 4, 5-triaryl and 1, 2, 4, 5-tetraaryl imidazoles using silica chloride as an efficient and recyclable catalyst under solvent-free conditions
HV Chavan, DK Narale - Comptes …, 2014 - comptes-rendus.academie-sciences …
Résumé An efficient solvent-free synthesis of various 2, 4, 5-triaryl imidazoles and 1, 2, 4, 5-
tetraaryl imidazoles has been developed using silica chloride as a heterogeneous catalyst …
tetraaryl imidazoles has been developed using silica chloride as a heterogeneous catalyst …
Iron-catalyzed alkenylation of Grignard reagents by enol phosphates
G Cahiez, O Gager, V Habiak - Synthesis, 2008 - thieme-connect.com
Stereoselective preparation of trisubstituted olefins can be easily performed from an Z/E-
mixture of enol phosphates by reacting only the E-isomer with a Grignard reagent in the …
mixture of enol phosphates by reacting only the E-isomer with a Grignard reagent in the …