Anabel Morcuende's research while affiliated with Instituto de Química Orgánica General and other places

What is this page?


This page lists the scientific contributions of an author, who either does not have a ResearchGate profile, or has not yet added these contributions to their profile.

It was automatically created by ResearchGate to create a record of this author's body of work. We create such pages to advance our goal of creating and maintaining the most comprehensive scientific repository possible. In doing so, we process publicly available (personal) data relating to the author as a member of the scientific community.

If you're a ResearchGate member, you can follow this page to keep up with this author's work.

If you are this author, and you don't want us to display this page anymore, please let us know.

Publications (10)


ChemInform Abstract: Biocatalysis in Organic Synthesis. Part 7. Enantioselective Transesterifications Catalyzed by an Acylase: Remarkable Influence of Remote Substitution and the Nature of the Solvent on the Selectivity
  • Article

September 2010

·

73 Reads

ChemInform

M. ORS

·

A. MORCUENDE

·

M. I. JIMENEZ-VACAS

·

[...]

·

ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.

Share

ChemInform Abstract: Regio- and Enantioselective Esterifications of Polyoxygenated Compounds Catalyzed by Lipases.

August 2010

·

6 Reads

ChemInform

ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.


ChemInform Abstract: Rapid Formation of Dibutylstannylene Acetals from Polyhydroxylated Compounds Under Microwave Heating. Application to the Regioselective Protection of Polyols and to a Catalytic Tin-Mediated Benzoylation.

August 2010

·

8 Reads

ChemInform

ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.


ChemInform Abstract: Microwave Accelerated Organic Transformations: Dibutylstannylene Acetal Mediated Selective Acylation of Polyols and Amino Alcohols Using Catalytic Amounts of Dibutyltin Oxide. Influence of the Solvent and the Power Output on the Selec

August 2010

·

9 Reads

ChemInform

ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.


ChemInform Abstract: Microwave-Promoted Transformations: Fast and Chemoselective N- Acylation of Amino Alcohols Using Catalytic Amounts of Dibutyltin Oxide. Influence of the Power Output and the Nature of the Acylating Agent on the Selectivity.

August 1996

·

11 Reads

·

56 Citations

The Journal of Organic Chemistry

The influence of the nature of the acylating agent and the power output on the chemoselectivity of the microwave-mediated acylation of 1,2- and 1,3-amino alcohols catalyzed by dibutyltin oxide has been studied. The method constitutes an efficient procedure for the selective N-acylation of amino alcohols.


Biocatalysis in Organic Synthesis 7. Enantioselective Transesterification Catalyzed by an Acylase: Remarkable Influence of Remote Substitution and the Nature of the Solvent on the Selectivity1

May 1996

·

18 Reads

·

29 Citations

Synlett

Acylase I from Aspergillus species catalyzes the reaction of transesterification between vinyl acetate and racemic derivatives of 2-(hydroxymethyl)piperidine. It has been found that the enantioselectivity of the reaction depends on the solvent. Also it has been observed that remote substituents have a great influence on the enantioselectivity.


Microwave Accelerated Organic Transformations: Dibutylstannylene Acetal Mediated Selective Acylation of Polyols and Amino Alcohols Using Catalytic Amounts of Dibutyltin Oxide. Influence of the Solvent and the Power Output on the Selectivity

May 1995

·

15 Reads

·

38 Citations

Synlett

The formation of dibutylstannylene acetals from polyols or amino alcohols and dibutyltin oxide is accelerated under microwave heating. We have found that under these conditions, only catalytic amounts of dibutyltin oxide (0.2 mol equiv.) are needed to achieve moderate to excellent conversions. The method is applied to the selective benzoylation of a variety of polyols and to an amino alcohol. The selectivity of the transformation can be modulated upon changes in some experimental variables (nature of the solvent and power output of the microwave oven).


Rapid Formation of Dibutylstannylene Acetals from Polyhydroxylated Compounds Under Microwave Heating. Application to the Regioselective Protection of Polyols and to a Catalytic Tin-Mediated Benzoylation

January 1994

·

12 Reads

·

43 Citations

Synlett

The formation of dibutylstannylene acetals from polyols and dibutyltin oxide is accelerated under microwave heating. The method is applied to the regioselective benzoylation of a variety of polyols. Some preliminary results on a catalytic tin-mediated benzoylation of polyols are also presented.



Regio- and enantioselective esterifications of polyoxygenated compounds catalyzed by lipases

May 1993

·

10 Reads

·

29 Citations

Tetrahedron Asymmetry

The lipase catalyzed esterifications of derivatives of propane-1,2,3-triol and butane-1,2,4-triol in organic solvents have been studied. The influence of several factors (lipase source, organic solvent, additives and structural variations in the substrates) on the selectivity have been investigated. Good levels of regio- and enantioselectivity have been achieved, providing practical methods for the synthesis of these chiral building blocks.

Citations (5)


... 7 Since Pasteur carried out the first resolution based on diastere-8 omeric salt formation, several resolution methods -such as 9 chromatographic separations or chemical and biochemical reac- 10 tions -have been developed. 11 Over the last decade the enzyme-catalyzed kinetic resolution 12 of racemic mixtures has become a common tool for preparation 13 of enantiomerically pure compounds. Conventionally enzymatic 14 reactions are performed in aqueous solutions, but many exam-15 ples indicate that enzymes are also active in organic solvents. ...

Reference:

Lipase-catalyzed enantioselective acylation of 3-benzyloxypropane-1,2-diol in supercritical carbon dioxide
Regio- and enantioselective esterifications of polyoxygenated compounds catalyzed by lipases
  • Citing Article
  • May 1993

Tetrahedron Asymmetry

... In connection with our long-standing interest on the structure (1-4) and reactivity (24)(25)(26)(27) of aromatic compounds, we have undertaken a thorough computational study on chlorinated biphenyls. Comprehensive research on the bioactivity of chlorinated biphenyls requires a complete set of physicochemical properties. ...

Biocatalysis in Organic Synthesis 7. Enantioselective Transesterification Catalyzed by an Acylase: Remarkable Influence of Remote Substitution and the Nature of the Solvent on the Selectivity1
  • Citing Article
  • May 1996

Synlett

... Supplementing dibutylstannylene acylation with microwave irradiation drastically reduced this reaction time to the order of 15 min. The resulting acylation occurred as a mixture of 2-O, 3-O, and 2,3-O modified monosaccharides, with prior primary hydroxyl protection; some unmodified carbohydrate remained when using either toluene or acetonitrile solvation [122]. ...

Microwave Accelerated Organic Transformations: Dibutylstannylene Acetal Mediated Selective Acylation of Polyols and Amino Alcohols Using Catalytic Amounts of Dibutyltin Oxide. Influence of the Solvent and the Power Output on the Selectivity
  • Citing Article
  • May 1995

Synlett

... Selective benzoylation of polyols occurs under MW irradiation conditions (84). The reaction carried out in the presence of dibutyltin oxide as solvent exclusively leads to the product that is benzoylated in the C-2 position (eq. ...

Rapid Formation of Dibutylstannylene Acetals from Polyhydroxylated Compounds Under Microwave Heating. Application to the Regioselective Protection of Polyols and to a Catalytic Tin-Mediated Benzoylation
  • Citing Article
  • January 1994

Synlett

... Selective N-acylation of amino alcohols was performed by using lipase [8] and dibutyltin oxide [9] as a catalyst, and both methods were conducted under microwave irradiation. N-Acylation of α, -diamino alcohol was also reported. ...

ChemInform Abstract: Microwave-Promoted Transformations: Fast and Chemoselective N- Acylation of Amino Alcohols Using Catalytic Amounts of Dibutyltin Oxide. Influence of the Power Output and the Nature of the Acylating Agent on the Selectivity.
  • Citing Article
  • August 1996

The Journal of Organic Chemistry