J. Béres

The first stereospecific synthesis of (+)-(1r,2s,4r)-4-amino-2-hydroxy-1-cyclopentanemethanol and (+)-carbocyclic thymidine.

László Ötvös, J. Béres, Gy. Sági et al. · Tetrahedron Letters · 1987 · 39 citations

-Carbocyclic Thymidine, Organic Chemistry, Stereoselective Synthesis +2

Stereospecific synthesis and antiviral properties of different enantiomerically pure carbocyclic 2'-deoxyribonucleoside analogs derived from common chiral pools: (+)-(1R,5S)- and (-)-(1S,5R)-2-oxabicyclo[3.3.0]oct-6-en-3-one

J. Béres, György Sági, I. Tömösközi et al. · Journal of Medicinal Chemistry · 1990 · 32 citations

Bioorganic Chemistry, Stereospecific Synthesis, Organic Chemistry +17

Stereospecific synthesis of (−)-carbocyclic 2',3'-Dideoxythymidine, a potential anti-aids agent.

J. Béres, Gy. Sági, I. Tömösközi et al. · Tetrahedron Letters · 1988 · 29 citations

Potential Anti-aids Agent, Medicinal Chemistry, Medicine +6

Study of the thermal behaviours of some metal acrylates

W. Balcerowiak, J. Hetper, J. Béres et al. · Journal of thermal analysis · 1977 · 24 citations

A highly efficient one-flask method for the preparation of the individual diastereoisomers of ribonucleoside 3',5'-cyclic N-substituted phosphoramidates via the direct Appel reaction. X-ray structure of trans-5-isopropyl-2'-deoxyuridine 3',5'-cyclic N-benzylphosphoramidate

J. Béres, Wesley G. Bentrude, Laszlo Parkanji et al. · The Journal of Organic Chemistry · 1985 · 23 citations

Direct Appel Reaction, Natural Product Synthesis, Engineering +11