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Dive into the research topics where Taleb H. Al-Tel is active.

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Featured researches published by Taleb H. Al-Tel.


Tetrahedron Letters | 1994

Synthesis of polyfunctionalized bis-annulated pyranosides: Useful intermediates for triquinane synthesis

Noshena Naz; Taleb H. Al-Tel; Yousef Al-Abed; Wolfgang Voelter

Abstract A mild method for the synthesis of bis-cyclopentanoids on carbohydrate templates using the Pauson-Khand reaction is described.


Tetrahedron Letters | 1993

Expeditious entries to chiral furanoids via pyranose annulation

Taleb H. Al-Tel; Yousef Al-Abed; Mohammed Saleh Shekhani; Wolfgang Voelter

Abstract A facile synthesis of polysubstituted ( Z )-tetrahydrofurylidenes using anhydrosugars is described. The ( Z )-compounds can be conveniently isomerized to the ( E )-products. The regiochemistry of the annulation reaction can be reversed by judicious choice of the leaving groups.


Tetrahedron Letters | 1998

A useful regioselective approach to episulfides via cis-oriented anhydro triflate sugars

Raed A. Al-Qawasmeh; Raid J. Abdel-Jalil; Taleb H. Al-Tel; René Thürmer; Wolfgang Voelter

An efficient method for the regioselective synthesis of episulfides, showing remarkable proteinase-inhibiting activity, from cis-oriented anhydro triflate sugars is decribed.


Tetrahedron | 1995

AN EFFICIENT ROUTE TO REGIO- AND STEREOSELECTIVE SYNTHESIS OF 3-AMINO-3-DEOXY SUGARS

Taleb H. Al-Tel; Raed A. Al-Qawasmeh; Christoph Schröder; Wolfgang Voelter

Abstract Starting from the trans-oriented hydroxy-epoxy pentoses (1, 8 and 15) and benzoylisocyanate a regio- and stereoselective route via the benzoylcarbamate intermediates 2, 9 and 16 to the 3-amino-3-deoxy sugars 7, 14 and 18 is described.


Tetrahedron Letters | 1995

A new strategy for carbohydrate-based syntheses of oxaspiro-multichiral systems: An alternative route to pyranosidic homologation

Taleb H. Al-Tel; Raed A. Al-Qawasmeh; Thomas Kaiser; Wolfgang Voelter

Abstract A new strategy for the syntheses of polyfunctionalized oxaspiro variants using furan and the keto sugars 1 and 6 is described. Also, the resulting satellite ring represents an alternative route to homologated pyranosides.


Tetrahedron Letters | 1995

Carbohydrates to carbocycles: Syntheses of polysubstituted chiral furanoids via oxirane ring opening

Taleb H. Al-Tel; Wolfgang Voelter

Abstract A new and effecient route to chiral furanoids through oxirane ring opening by the dianions of β-dicarbonyl compounds followed by intramolecular ring-closure is described. Furthermore, the syntheses of γ-lactones fused at C-2 and C-3 of the pyranosidic ring is also achieved.


Natural Product Letters | 1994

Chiral δ-lactones via Pyranose-annulation

Yousef Al-Abed; Taleb H. Al-Tel; Mohammed Saleh Shekhani; Wolfgang Voelter

Abstract The syntheses of chiral δ-lactones 6, 10, 11a,b and 12 from anhydro riboses 1 and 7a,b are described.


Journal of Organic Chemistry | 1996

PALLADIUM-COBALT-MEDIATED DOUBLE ANNULATION PROCESS : A NEW STRATEGY TO CHIRAL AND POLYSUBSTITUTED BIS-CYCLOPENTANOIDS ON CARBOHYDRATE PRECURSORS

Noshena Naz; Taleb H. Al-Tel; Yousef Al-Abed; Wolfgang Voelter; R. Ficker; W. Hiller


Liebigs Annalen | 1995

Eine neue Synthesestrategie zur Darstellung chiraler, polysubstituierter, an Pyranosen anellierter Tetrahydrofurane

Taleb H. Al-Tel; Mark Meisenbach; Wolfgang Voelter


Chemistry Letters | 1999

Carbohydrates to heterocycles: A new strategy for the synthesis of enantiomerically pure pyridazines and oxazines derived from epoxypyranoside scaffolds

Raed A. Al-Qawasmeh; Taleb H. Al-Tel; Raid J. Abdel-Jalil; Wolfgang Voelter

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Noshena Naz

University of Tübingen

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