Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Abdallah Ezzitouni"'
Publikováno v:
Organic Process Research & Development. 13:581-583
A simple, inexpensive, one-step general procedure was developed for the preparation of medium-chain fatty acid (MCFA) metal salts. This approach offers the advantage of a practical route and is superior to literature methods. Also, it overcomes many
Autor:
Clifford George, Joseph J. Barchi, Victor E. Marquez, Maqbool A. Siddiqui, Ron J. Feldman, Pamela Russ, Abdallah Ezzitouni, Hiroaki Mitsuya, Harry Ford
Publikováno v:
Nucleosides and Nucleotides. 17:1881-1884
Two conformationally locked carba-AZT nucleoside 5′-triphosphates built on a rigid bicyclo[3.1.0]hexane template showed exclusive Northern (2E) and Southern (3E) conformations, respectively. Inhibition of reverse transcriptase (RT) occurred selecti
Autor:
Victor E. Marquez, Clifford George, Hiroaki Mitsuya, Abdallah Ezzitouni, Harry Ford, Pamela Russ, Ron J. Feldman, Joseph J. Barchi, Maqbool A. Siddiqui
Publikováno v:
Journal of the American Chemical Society. 120:2780-2789
It has been proposed that the preference of 3‘-azido-3‘-deoxythymidine (AZT) for the extreme 3E (south) conformation, as observed in its X-ray structure, is responsible for its potent anti-HIV acti...
Publikováno v:
The Journal of Organic Chemistry. 62:4870-4873
Autor:
Clifford George, Victor E. Marquez, Maqbool A. Siddiqui, Pamela Russ, Abdallah Ezzitouni, Hisafumi Ikeda
Publikováno v:
Nucleosides and Nucleotides. 16:1431-1434
A conformational analysis of carbocyclic nucleosides built on a rigid bicyclo[3.1.0]hexane template (1–4, Northern and 5–8 Southern) showed that the Northern conformation prefers an anti glycosyl torsion angle whereas the Southern conformation fa
Publikováno v:
Tetrahedron Letters. 38:723-726
In a functionalized cyclopentene having allylic OH and NH-acyl groups on opposite faces of the ring, the diastereoselective delivery of the incoming methylene group in the diethylzinc version of the Simmons-Smith reaction was completely directed by t
Autor:
Victor E. Marquez, Abdallah Ezzitouni
Publikováno v:
Journal of the Chemical Society, Perkin Transactions 1. :1073-1078
The construction of carbocyclic nucleosides with a fixed 3E ring pucker in the Southern hemisphere of the pseudorotational cycle is achieved from a common precursor carbocyclic amine, (1S,3S,4R,5 S )-3-benzyloxy-4-benzyloxymethyl-1-aminobicyclo[3.1.0
Autor:
Victor E. Marquez, Pamela Russ, Abdallah Ezzitouni, Maqbool A. Siddiqui, Mark D. Matteucci, Richard W. Wagner, Jianying Wang
Publikováno v:
Journal of Medicinal Chemistry. 39:3739-3747
The sugar moiety of nucleosides in solution is known to exist in a rapid dynamic equilibrium between extreme Northern and Southern conformations as defined in the pseudorotational cycle. In the present work, we describe how the bicyclo[3.1.0]hexane t
Publikováno v:
Tetrahedron Letters. 34:315-318
Three 2′, 3′-unsaturated pyrimidine nucleosides, bearing an azido-methyl group at 2′ or 3′ were synthesized as potential anti-HIV agents. The key step involves an SN2′ opening of 2, 2′ or 2, 3′-anhydronucleosides by azide ion.
Publikováno v:
ChemInform. 22
Starting from 1,2-O-isopropylidene-α-D-xylofuranose, a versatile method for the synthesis of branched 3'-deoxy-2',3'-didehydro nucleosides is described and exemplified for an analogue of 3'-deoxy-2',3'-didehydrothymidine (d4T)