Mentioned in

References in periodicals archive

Hu, "Nanoparticle based on poly(ionic liquid) as an efficient solid immobilization catalyst for aldol reaction and multicomponent reaction in water," ACS Applied Materials & Interfaces, vol.

Optimization of Process Variables in the Synthesis of Tributyl Citrate Using a Polyvinylpolypyrrolidone-Supported Bronsted Acidic Ionic Liquid Catalyst

The organocatalytic aldol reaction [1] is one of the most powerful methods for forming C-C bonds in a highly stereocontrolled manner.

An Investigation of the Enolization and Isomeric Products Distribution in the Water Promoted Aldol Reaction of Tropinone and Granatanone

reported the application of the chiral ionic liquid 1 and its derivatives as an organocatalyst for aldol reaction; however, the aldol products were obtained in moderate yields and selectivities (up to 80% ee) [18].

Proline based chiral ionic liquids for enantioselective Michael reaction

Extending the coverage of its predecessor, Modern Aldo Reactions, this reference focuses on the latest developments and offers new tools for use of the aldol reaction in the development of natural products and pharmaceuticals.

Modern methods in stereoselective aldol reactions

Moreover, PEG is inexpensive, easy to handle, thermally stable, non-toxic, and recyclable in various organic transformations [21], such as for example, Heck reaction [22], catalytic hydrogenations [23], asymmetric dihydroxylation reaction [24], Baylis-Hillman reaction [25], Biginelli reaction [26], Suzuki-Miyaura reaction, Stille cross-coupling reaction [27], Wacker reaction [28] and asymmetric aldol reaction [29].

PEG-400 as an efficient and recyclable reaction medium for the synthesis of polyhydroquinolines via Hantzsch reaction

Key steps included a diisopinocampheylchloroborane (DPC)-catalysed aldol reaction that was shown to be highly sensitive to traces of moisture.

Boron from lab to launch: Christopher D. Hewitt and Karl Matos from BASF Corporation, USA, review recent developments in the use of borane reagents for commercial-scale API synthesis, which were highlighted when more than 150 scientists met at the 5th BASF Boron Conference in March 2009 in Hyderabad, India

A recent communication from the Journal of Organic Chemistry describing an asymmetric, biologically-catalyzed aldol reaction was used as the basis for this study.

Chemistry section. (Collegiate Division 2002)

Triacetone alcohol and semiphorone undergo retrograde aldol reaction catalyzed by carbonaceous residues adhering to the surface of the injector port of the gas chromatograph during GC-MS analysis.

THERMAL DECOMPOSITION OF ACETONE TRIMERS DURING GC-MS ANALYSIS

Some examples have been reported on the use of organocatalysts in water which is an important approach to the principles of green chemistry [5].The aldol reaction is one of the mostimportant carbon-carbon bond forming reactions in modern organic synthesis as a key step in natural product synthesis and for the rapid access to polyoxygenated compounds.

Investigation of Proline Amides and Pyridinium Salts as Catalyst for Direct Aldol Reactions in Water

The thermoresponsive polymer in water aggregate to form a rather hydrophobic reaction field and the substrates are probably concentrated and promoted the aldol reaction in the resulting hydrophobic field.

Thermoresponsive and redox behaviors of poly(N-isopropylacrylamide)-based block copolymers having TEMPO groups as their side chains