A New Procedure for Dethioacetalization via Equilibrium Exchange with Aqueous Acetone, Paraformaldehyde and Amberlyst 15 as Acidic Catalyst

DOI: 10.1055/s-1990-26870

Source and publish data:

Synthesis p. 336 - 337 (1990)

Update date:2022-08-29

Topics:

Authors:

Ballini, Roberto

Petrini, Marino

Read Full Text PDF DownLoad Join now for total 90,000,000 free articles

Article abstract of DOI:10.1055/s-1990-26870

Carbonyl compounds were regenerated from corresponding Ethanediyl S,S-Acetals via equilibrium exchange with aqueous acetone, paraformaldehyde and Amberlyst 15, as acidic catalyst, at 80 deg C.

Full text of DOI:10.1055/s-1990-26870

Products guided by the article

Product name:Benzaldehyde

Cas No:100-52-7

Relevant to this article

Organic fluorescent molecule with high solid state luminescent efficiency and protonation stimuli-response

Doi:10.1002/cjoc.201300583
(2013)
Doi:10.1021/ja01243a510
(1943)
Basic Methanolysis of N-Aryl-N-phenylbenzamides

Doi:10.1021/jo01300a028
(1980)
Synthesis and characterization of thienorphine and its glucuronide conjugate

Doi:10.1081/SCC-200050367
(2005)
First synthesis and characterization of SRR/RSS-Ezetimibe

Doi:10.1016/j.tetlet.2013.09.049
(2013)
Mechanism of the N-cyclopropylimine-1-pyrroline photorearrangement

Doi:10.1021/ja0467566
(2005)

Article Doi

A New Procedure for Dethioacetalization via Equilibrium Exchange with Aqueous Acetone, Paraformaldehyde and Amberlyst 15 as Acidic Catalyst

DOI: 10.1055/s-1990-26870

Source and publish data:

Authors:

Article abstract of DOI:10.1055/s-1990-26870

Full text of DOI:10.1055/s-1990-26870

Products guided by the article

Relevant to this article

Hot Product