Novel Synthesis of a New Class of Polynuclear Pyridinethione Nucleosides
摘要:
A novel synthesis of a new class of polynuclear pyridinethione glycosides utilizing the reactions of phenanthridine analogues and proportional to-bromoglucose or proportional to-bromogalactose tetraacetate as starting components is described.
Rearrangement studies on 1-tetralylidenecyanothioacetamide: A different novel synthetic routes to strong fluorescent phenanthridine and phenanthrene analogues
摘要:
A novel synthesis of strong fluorescent phenanthridine and phenanthrene analogues utilizing arylmethylenecyanothioacetamides and 1-tetralylidenemalononitrile or 1-tetralylidenecyanothioacetamide and arylmethylenemalononitriles as starting components is described.
NUCLEIC ACID COMPONENTS AND THEIR ANALOGUES: A NOVEL AND EFFICIENT METHOD FOR THE SYNTHESIS OF A NEW CLASS OF BIPYRIDYL AND BIHETEROCYCLIC-NITRO GEN THIOGLYCOSIDES FROM PYRIDINE-2(1H)-THIONES
作者:Galal H. Elgemeie、Mervat M. El-Enany、Mohamed M. Ismail、Eman K. Ahmed
DOI:10.1081/ncn-120014820
日期:——
ABSTRACT A novelsynthesis of a new class of bipyridyl and biheterocyclic-nitrogen thioglycosides utilizing the reactions of heterocyclic substituted pyridine-2(1H)-thiones and α-bromoglucose or α-bromogalactose tetraacetate as starting components is described.
Rearrangement studies on 1-tetralylidenecyanothioacetamide: A different novel synthetic routes to strong fluorescent phenanthridine and phenanthrene analogues
作者:Galal E.H. Elgemeie、Nahed M. Fathy
DOI:10.1016/0040-4020(95)00063-e
日期:1995.3
A novel synthesis of strong fluorescent phenanthridine and phenanthrene analogues utilizing arylmethylenecyanothioacetamides and 1-tetralylidenemalononitrile or 1-tetralylidenecyanothioacetamide and arylmethylenemalononitriles as starting components is described.
Novel Synthesis of a New Class of Polynuclear Pyridinethione Nucleosides
作者:Galal E. H. Elgemeie、Adel M. E. Attia、Nahed M. Fathy
DOI:10.1080/07328319708001365
日期:1997.4
A novel synthesis of a new class of polynuclear pyridinethione glycosides utilizing the reactions of phenanthridine analogues and proportional to-bromoglucose or proportional to-bromogalactose tetraacetate as starting components is described.