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Research paper thumbnail of ChemInform Abstract: Use of O,Se-Acetals for Radical-Mediated Phenylseleno Group Transfer Reactions

Cheminform, 2010

ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was e... more 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.

Research paper thumbnail of A Non-Racemic Equivalent of Glycolic Acid: Preparation of both enantiomers fromD-mannitol

Helvetica Chimica Acta, 1996

A practical synthesis of both enantiomers of 2-(tert-butyl)-2-methyl-1,3-dioxolan-4-one starting ... more A practical synthesis of both enantiomers of 2-(tert-butyl)-2-methyl-1,3-dioxolan-4-one starting from D-mannitol is reported. These compounds are chiral equivalents of glycolic acid (= hydroxyacetic acid) which are configurationally stable and can be alkylated via their enolates.

Research paper thumbnail of Use of O,Se-Acetals for Radical-Mediated Phenylseleno Group Transfer Reactions

Synthesis-stuttgart, 1996

Ester substituted O, Se-acetals are very efficient radical precursors which can be used for inter... more Ester substituted O, Se-acetals are very efficient radical precursors which can be used for intermolecular formation of CC bonds via phenylseleno group transfer. The nucleophilic nature of the radical intermediates has been demonstrated and good yields were obtained ...

Research paper thumbnail of ChemInform Abstract: Preparation of 1‐Hydroxycyclopentanecarboxylic Acid Derivatives from a Chiral Equivalent of Glycolic Acid.

Research paper thumbnail of Preparation of 1‐Hydroxycyclopentanecarboxylic Acid Derivatives from a Chiral Equivalent of Glycolic Acid

European journal of …, Jan 1, 1999

... Full Paper. Preparation of 1-Hydroxycyclopentanecarboxylic Acid Derivatives from a Chiral Equ... more ... Full Paper. Preparation of 1-Hydroxycyclopentanecarboxylic Acid Derivatives from a Chiral Equivalent of Glycolic Acid. Sokol Abazi 1 ,; Liliana Parra Rapado 1 ,; Kurt Schenk 2 ,; Philippe Renaud. Article first published online: 18 JAN 1999. ...

Research paper thumbnail of Diastereoselective Radical Mediated Alkylation of a Chiral Glycolic Acid Derivative

Organic & Biomolecular Chemistry, Jan 1, 2011

Research paper thumbnail of ChemInform Abstract: Radical Cascade Processes Leading to Fused‐and Spiro‐Bicyclic Ring Systems.

Research paper thumbnail of ChemInform Abstract: Use of O,Se-Acetals for Radical-Mediated Phenylseleno Group Transfer Reactions

Cheminform, 2010

ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was e... more 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.

Research paper thumbnail of A Non-Racemic Equivalent of Glycolic Acid: Preparation of both enantiomers fromD-mannitol

Helvetica Chimica Acta, 1996

A practical synthesis of both enantiomers of 2-(tert-butyl)-2-methyl-1,3-dioxolan-4-one starting ... more A practical synthesis of both enantiomers of 2-(tert-butyl)-2-methyl-1,3-dioxolan-4-one starting from D-mannitol is reported. These compounds are chiral equivalents of glycolic acid (= hydroxyacetic acid) which are configurationally stable and can be alkylated via their enolates.

Research paper thumbnail of Use of O,Se-Acetals for Radical-Mediated Phenylseleno Group Transfer Reactions

Synthesis-stuttgart, 1996

Ester substituted O, Se-acetals are very efficient radical precursors which can be used for inter... more Ester substituted O, Se-acetals are very efficient radical precursors which can be used for intermolecular formation of CC bonds via phenylseleno group transfer. The nucleophilic nature of the radical intermediates has been demonstrated and good yields were obtained ...

Research paper thumbnail of ChemInform Abstract: Preparation of 1‐Hydroxycyclopentanecarboxylic Acid Derivatives from a Chiral Equivalent of Glycolic Acid.

Research paper thumbnail of Preparation of 1‐Hydroxycyclopentanecarboxylic Acid Derivatives from a Chiral Equivalent of Glycolic Acid

European journal of …, Jan 1, 1999

... Full Paper. Preparation of 1-Hydroxycyclopentanecarboxylic Acid Derivatives from a Chiral Equ... more ... Full Paper. Preparation of 1-Hydroxycyclopentanecarboxylic Acid Derivatives from a Chiral Equivalent of Glycolic Acid. Sokol Abazi 1 ,; Liliana Parra Rapado 1 ,; Kurt Schenk 2 ,; Philippe Renaud. Article first published online: 18 JAN 1999. ...

Research paper thumbnail of Diastereoselective Radical Mediated Alkylation of a Chiral Glycolic Acid Derivative

Organic & Biomolecular Chemistry, Jan 1, 2011

Research paper thumbnail of ChemInform Abstract: Radical Cascade Processes Leading to Fused‐and Spiro‐Bicyclic Ring Systems.

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