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Results: 1-10 |
Results: 10
ENZYMES AND PROTECTING GROUP CHEMISTRY
Authors: PATHAK T WALDMANN H
Citation: T. Pathak et H. Waldmann, ENZYMES AND PROTECTING GROUP CHEMISTRY, CURRENT OPINION IN CHEMICAL BIOLOGY, 2(1), 1998, pp. 112-120
SUGAR-MODIFIED URIDINE BISVINYL SULFONE - SYNTHESIS OF A BIFUNCTIONALIZED NUCLEOSIDE MICHAEL ACCEPTOR AND ITS USE IN STEREOSELECTIVE TANDEMCYCLIZATION
Authors: BERA S LANGLEY GJ PATHAK T
Citation: S. Bera et al., SUGAR-MODIFIED URIDINE BISVINYL SULFONE - SYNTHESIS OF A BIFUNCTIONALIZED NUCLEOSIDE MICHAEL ACCEPTOR AND ITS USE IN STEREOSELECTIVE TANDEMCYCLIZATION, Journal of organic chemistry, 63(6), 1998, pp. 1754-1760
5'-O-BENZOYL-2',3'-DIDEOXY-2'-OXO-ALPHA-URIDINE
Authors: SURESH CG SAKTHIVEL K PATHAK T
Citation: Cg. Suresh et al., 5'-O-BENZOYL-2',3'-DIDEOXY-2'-OXO-ALPHA-URIDINE, Acta crystallographica. Section C, Crystal structure communications, 52, 1996, pp. 1776-1779
5'-O-BENZOYL-2'-KETO-3'-DEOXY-ALPHA-URIDINE - FIRST UNAMBIGUOUS SYNTHESIS, CRYSTAL-STRUCTURE AND ITS USE TO ESTABLISH THE ANOMERIZATION OF 2'-KETOURIDINES UNDER BASIC CONDITIONS
Authors: SAKTHIVEL K PATHAK T SURESH CG
Citation: K. Sakthivel et al., 5'-O-BENZOYL-2'-KETO-3'-DEOXY-ALPHA-URIDINE - FIRST UNAMBIGUOUS SYNTHESIS, CRYSTAL-STRUCTURE AND ITS USE TO ESTABLISH THE ANOMERIZATION OF 2'-KETOURIDINES UNDER BASIC CONDITIONS, Tetrahedron, 52(5), 1996, pp. 1767-1772
ONE-POT DEOXYGENATIVE CONVERSION OF A-RIBONUCLEOSIDE TO ENAMINONUCLEOSIDES INVOLVING 1,2-HYDRIDE SHIFT REARRANGEMENT
Authors: SAKTHIVEL K PATHAK T
Citation: K. Sakthivel et T. Pathak, ONE-POT DEOXYGENATIVE CONVERSION OF A-RIBONUCLEOSIDE TO ENAMINONUCLEOSIDES INVOLVING 1,2-HYDRIDE SHIFT REARRANGEMENT, Tetrahedron, 52(13), 1996, pp. 4877-4882
OPENING OF 2',3'-O-ANHYDRO-RING OF 2',3'-O-ANHYDRO-LYXO-URIDINE BY ALKYLAMINES AND ARYLAMINES - EASY SYNTHESES AND PREPARATIVE USES OF 2'-DEOXY-2'-ALKYLAMINO-XYLO-URIDINES AND 3'-DEOXY-3'-ALKYLAMINO-ARA-URIDINES
Authors: BERA S PATHAK T LANGLEY GJ
Citation: S. Bera et al., OPENING OF 2',3'-O-ANHYDRO-RING OF 2',3'-O-ANHYDRO-LYXO-URIDINE BY ALKYLAMINES AND ARYLAMINES - EASY SYNTHESES AND PREPARATIVE USES OF 2'-DEOXY-2'-ALKYLAMINO-XYLO-URIDINES AND 3'-DEOXY-3'-ALKYLAMINO-ARA-URIDINES, Tetrahedron, 51(5), 1995, pp. 1459-1470
3'-DEOXY-3'-(VINYLSULPHONYL)THYMIDINE - A NEW REACTIVE ANALOG OF AZT - ITS SYNTHESIS AND REACTIVITIES TOWARDS VARIOUS NUCLEOPHILES
Authors: BERA S SAKTHIVEL K PATHAK T LANGLEY GJ
Citation: S. Bera et al., 3'-DEOXY-3'-(VINYLSULPHONYL)THYMIDINE - A NEW REACTIVE ANALOG OF AZT - ITS SYNTHESIS AND REACTIVITIES TOWARDS VARIOUS NUCLEOPHILES, Tetrahedron, 51(28), 1995, pp. 7857-7866
REACTIONS OF 2',3'-DI-O-MESYL-LYXO-URIDINE WITH SECONDARY-AMINES - FIRST REPORT ON THE ONE-POT CONVERSION OF MESYLATED NUCLEOSIDES TO ENAMINONUCLEOSIDES AND THE CRYSTAL-STRUCTURE OF ALPHA-ENAMINE
Authors: SAKTHIVEL K PATHAK T SURESH CG
Citation: K. Sakthivel et al., REACTIONS OF 2',3'-DI-O-MESYL-LYXO-URIDINE WITH SECONDARY-AMINES - FIRST REPORT ON THE ONE-POT CONVERSION OF MESYLATED NUCLEOSIDES TO ENAMINONUCLEOSIDES AND THE CRYSTAL-STRUCTURE OF ALPHA-ENAMINE, Tetrahedron, 50(46), 1994, pp. 13251-13260
ONE-STEP SYNTHESIS OF C-2 DIALKYLAMINO-SUBSTITUTED 2',3'-O-ANHYDRO-LYXO-URIDINES - 1ST REPORT ON THE OPENING OF 2,2'-O-ANHYDRO-BRIDGE OF 2,2'-O-ANHYDROURIDINE BY SECONDARY-AMINES
Authors: SAKTHIVEL K BERA S PATHAK T
Citation: K. Sakthivel et al., ONE-STEP SYNTHESIS OF C-2 DIALKYLAMINO-SUBSTITUTED 2',3'-O-ANHYDRO-LYXO-URIDINES - 1ST REPORT ON THE OPENING OF 2,2'-O-ANHYDRO-BRIDGE OF 2,2'-O-ANHYDROURIDINE BY SECONDARY-AMINES, Tetrahedron, 49(45), 1993, pp. 10387-10392
REACTIONS OF DIMESYLTHYMIDINE WITH SECONDARY-AMINES - EASY ACCESS TO ,5'-DIDEOXY-3'-SUBSTITUTED-5'-ALKYLAMINOTHYMIDINES - NEW CLASSES OF POTENTIAL ANTIVIRAL AMINONUCLEOSIDES
Authors: SAKTHIVEL K KUMAR RK PATHAK T
Citation: K. Sakthivel et al., REACTIONS OF DIMESYLTHYMIDINE WITH SECONDARY-AMINES - EASY ACCESS TO ,5'-DIDEOXY-3'-SUBSTITUTED-5'-ALKYLAMINOTHYMIDINES - NEW CLASSES OF POTENTIAL ANTIVIRAL AMINONUCLEOSIDES, Tetrahedron, 49(20), 1993, pp. 4365-4372
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